02
PLANT SCIENCES FEED
REVIEW ARTICLE
2012
ISSN : 2231 - 1971
http://psf.lifescifeed.com
TAXONOMY AND PHYSIOLOGICAL STUDIES IN SPIDER FLOWER
(CLEOME SPECIES): A CRITICAL REVIEW
VISHAL T. APARADH*, RAHUL J. MAHAMUNI AND B. A. KARADGE
Cleomaceae is a small family of flowering plants in the order Brassicales, comprising more than 300 species
belonging to 9 genera of which Cleome is the largest genus with about 180 - 200 species of medicinal,
ethnobotanical, ecological importance. The present paper accounts for critical review of spider flower
genus Cleome with special emphasis on its taxonomy, ecology, ethnobotany, cytology, biochemistry,
physiology and pathology with a note on its importance. The review of the researches on Cleome will
provide understanding the value of the species and guidelines for further researches with spider flower
genus.
KEYWORDS : Taxonomy, Physiology, Cytology, Ethnobotany, Pathology, Cleome, Spider Flower
Cite this article as :
Aparadh et al. (2012). Taxonomy and Physiological Studies In Spider Flower (Cleome species): A Critical
Review. Plant Sciences Feed 2 (3) : 25- 46
AUTHOR AFFILIATIONS:
AUTHOR EMAIL
Department of Botany, Shivaji University, Kolhapur (Maharashtra) India. 416 004.
vishu1415@gmail.com
1. INTRODUCTION
Cleome is the largest genus from family Cleomaceae
comprising 180 to 200 species of herbaceous annual or
gynandra grow throughout the year but more vigorously
during rainy season. C. gynandra grows predominantly in
waste places along waste water. C. speciosa is cultivated
perennial plants and shrubs widely distributed in tropical
species growing widely in shadow places in the red soil
species have been recorded [1]. In India, the genus is
gardens.
and subtropical regions. The major diversity of Cleome is
restricted to tropical regions, where approximately 150
represented by fifteen species [2], 12 are reported in
Maharashtra [3], while seven from Kolhapur district [4].
Earlier floristic workers like Hooker and Thomson [5] and
Cooke [6] put Cleome and other allied genera under the
family Capparidaceae, however, recently all these genera
are separated taxonomically and put under a separate
family i.e. Cleomaceae. Many of workers previously treated
this genus in family Capparaceae, until DNA studies (APG II
system) found that the major Cleomaceae members are
closer to Brassicaceae than Capparaceae [7].
The genus Cleome is under constant evolution, many
species show a developmental progression from C3
photosynthesis to C4 photosynthesis and this evolutionary
progression is identical to Brassicaceae members like
Arabidopsis thaliana [8]. There is very scanty and scattered
work in the genus Cleome. Particularly, the anatomical and
physiological studies in the species are rare.
Present exploration is strictly carried out for selective
species of Cleome viz. Cleome chelidonii L.f., C. speciosa Raf.,
C. gynandra L., C. simplicifolia (Camb.) Hook f. & Thoms and
C. viscosa L.. All these species are herbs growing at same
locality but in different soil types as Cleome chelidonii grows
vigorously in moist places and also in the rocky regions,
while C. simplicifolia and C. viscosa grow luxuriantly in the
black soil in rainy season. Cleome simplisifolia has very
short life cycle up to 3-4 months only. C. viscosa and C.
particularly during rainy season. It is famous for its
beautiful showy inflorescence and hence cultivated in
Cleome is known by various names such as spider flower
and mountain bee plant. The indigenous knowledge of
many traditional communities has been formulated,
documented, and ultimately become organized systems of
medicine, such as Ayurveda, Siddha, Unani, and other
systems outside India.
Cleome has traditionally known for its different medicinal
properties like leaf paste on headache, leaf juice of Cleome
gynandra on earache and skin diseases. It is also used in
food in African countries mostly for pregnant women.
Boiled leaves of Cleome serrulata are used in preparation of
black paint. Species like Cleome viscosa, Cleome gynandra
and Cleome chelidonii have many medicinal applications,
often in rubifacient and counter irritant preparations. They
are also used for rheumatism and even headache [9].
Cleome viscosa is bushy aromatic herb with glandular
trichomes, seeds of which are said to be anthelmintic and
useful in fever, diarrhea and infantile convulsion [10].
Cleome viscosa is a popular remedy for a variety of ailments
as documented in ethnobotanical surveys and traditional
systems of medicine, such as Ayurveda and Unani [11].
A brief comparative account of the species which have been
undertaken for the present study, with respect to their
occurance or distribution, their habit, some morphological
traits and flowering period, has been recorded in the
following Table.1
Table 1 A brief comparative account of habitat in Cleome species
Soil type needed
Habitat
C. simplicifolia
Africa and S.
Arabia to
Australia
India
Annual erect
herb
Annual Semierrect/ prostrate
herb
Red and black
both
Black
Plant Sciences Feed Vol. 2 Issue 3
C. gynandra
C. chelidonii
Shrilanka to India to
whole Asia
India
Annual herb
Annual herb
Black mostly with
waste place
Moist black/soil
form due to rock
erosion
C. speciosa
Tropical America.
Redish
semi-shrub
26
Native
C. viscosa
Page
Characters/
Other
Flower colour
Androecium
Gynoecium
Capsule (length)
Simple
Mostly 5 foliate
pinnately compound
Axillary
racemes
Solitary axillary
Corymbose - racemes
Many
6
Yellow
Violet / pink
Gynophore
absent
Gynophore
absent
Many
Seed
5-7 cm
Flowering and
Fruiting
Throughout
year
brownish-black
Subglobose
2-4 cm
Brown
August - Nov.
Economically the genus Cleome is not such admired.
However, in many African countries some species are
cultivated for their foliage which has some medicinal
properties. Some species like C. gynandra are eaten as
vegetable in extreme conditions. Besides, major Cleome
species are considered and ignored as a weed in several
countries. Species like C. speciosa, C. hassleriana, C. serrulata
are commonly planted in gardens or on the hedges for their
striking inflorescence. Seeds of all Cleome species are horse
shoe shaped, containig upto 17to 19% of oil. Oil of Cleome
seeds has insect repellent properties so used against tick.
Seeds of Cleome chelidonii are used as condiment (Flora of
India vol 2). Seeds are rich in unsaturated fatty acid as
linoleic acid and phytosterol [12].
2. TAXONOMY OF CLEOME
Cleome species were put earlier in family
Capparidaceae. However, recently the genus has been given
a separate status. It has been separated from
Capparidaceae and grouped as Cleomaceae. Cooke [6] has
described ten species of Cleome under Capparidaceae. One
hundred and fifty Cleome spp. have been so far described
worldwide in tropical regions [13] and fifteen species occur
in India. Seven species are found to be distributed in the
region of Kolhapur district [4].
There are lots of observations on different parts of
Cleome species and some new species have been described
continuously from past century by different authors.
Diagnosen and Kleinere [14] have reported a new species
Cleome schweinfurthii. Kers [15] has described Cleome
uncifer from Northwest Australia. Cleome kersiana has been
Simple leaves also
at basal region
Axillary and
terminal racemes
White
Violet / pink
Gynandrophore 1cm
long
Gynophore absent
Muricate, dark
brown, globose
Grey brown
4-8cm
August- Dec
3-7 foliate
pinnately
compound
racemes
pink / purple
Many
6
5-8 cm
3-6cm
Grey black
August- Oct.
Sept. - Dec
Gynophore
elongated
described and illustrated by Thulin [16] from Somalia. Iltis
and Ruiz [17] have described endemic species Cleome
torticarpa from wet gallery forests National Park,
Venezuela. Silva [18] from Brazil reported Cleome eosina J.
F. Macbr. which was considered endemic to Paraguay.
Reddy and Raju [19] have reported Cleome chelidonii var
pallai as a new variety from India. Keighery [20] has
discussed nomenclature and taxanomy of Cleome uncifera
and he separated it as a new subspecies using leaf
morphology, a small-leaved variant species named Cleome
uncifera subsp. microphylla Kers. and discused ranges of
variation in the leaves of the new and typical subspecies.
Iltis [21] has described and illustrated Cleome boliviensis
Iltis, with large-flowers, and discussed its relationship to
other species.
Durand and Durand [22] have described six species of
Cleome under Sylloge Flora Congolanae. Two new species,
Cleome viscosa, C. spinosa and also Cleome gynandra have
been described by Wilczek [23] from Bas Katanga district.
Blacklock [24] has described upto 8 species of Cleome from
flora of Iraq and has given a separate key for their
identification. Rao [25] reported for the first time Cleome
rutidosperma from Andaman and Nicobar Islands. Weber et
al. [26] have added Cleome serrulata to the flora of
Colorado USA. Chamberlain et al. [27] have recorded two
new combinations and formal descriptions for eight new
species and three new subspecies for the genera Cleome,
Polycarpaea, Silene, Gypsophila, Dianthus and Rubus in
Volume I of the Flora of the Arabian Peninsula and Socotra.
Siwakoti and Verma [28] have reported Cleome
rutidosperma DC.and C. spinosa Jacq. with other eighteen
27
Inflorescence
3-5 foliate
pinnately
compound
Page
Leaves
Mostly 3
sometime upto 7
foliate pinnately
compound;
Plant Sciences Feed Vol. 2 Issue 3
Many workers have studied pollen morphology of
different Cleome species. Pope [37] studied pollen colours
in different families and concluded that colour of pollen
grains is almost constant in almost all members of a
particular family with few exceptions. He studied Cleome
and observed green coloured pollens in it. Mitra [38] has
studied pollen morphology in some Cleome species.
Solomon et al. [39] studied the pollen morphology of
Cleome serrulata and reported that they are prolate,
tricolporate, tectum reticulate with micropunctate lamina.
Flint and Martyn [40] worked on pollen germination and
they mentioned that when UVB was administerd a large
and significant inhibition of pollen germination was noted
in Cleome lutea. Palacios et al. [41] studied the pollen grains
of three taxa belonging to family Capparidaceae, Cleome
multicaulis, Cleomella mexicana and Polanisia uniglandulosa
and suggested that the species could be separated on the
basis of the characteristics of seeds such as the
ornamentation, apertures and shape. Ruiz et al. [42]
Plant Sciences Feed Vol. 2 Issue 3
Gier [46] prepared a key for identification of
herbaceous dicotyledons and studied the morphology of
Cleome serrulata and reported the absence of stipules in it.
Guedes [47] studied morphology and anatomy of Cleome
simplicifolia and for the first time he described the peltate
petals in it. Puri [48] studied the morphology of leaf and
seeds of Cleome gynandra. Bhattacharya and Maiti [49]
from BSI studied seed morphology of 12 species of Cleome
and prepared a taxonomic key for their identification
through seeds only. Chakrabarty and Gupta [50] have
reported morphohistological characters of 3 herbaceous
species growing along railway track including Cleome
viscosa L. Sereno [51] from Caribbean Barbados region has
studied the morphology of Cleome tenuis. Ruiz and Escale
[52] studied seed morphology of 19 species of Cleome L.
from Venezuela using the scanning electron microscope
and observed seminal characters. Richard et al. [53]
described morphological details of Cleome isomeris and C.
viscosa. Thulin [54] has studied morphology of four species
of Cleome in the Horn of Africa region and reported that C.
omanensis, comb. nov. occurs in the Mahrah Region of
Yemen and also in Oman and prepared a key for
identification of the species.
According to Smith [55] a gynophore is usually defined
as stalk or stip which supports the ovary or gynoecium in
certain flowers of Cleome. Vanderpool [56] in his studies on
SEM of seeds of some Cleome species found the presence of
stomates on the seeds. Lloyd et al. [57] reported occurrence
of heterostyly in S. African species of Bauhinia
(Leguminosae),
Cleome
(Capparaceae),
Aneilema
(Commelinaceae), and Agelaea (Connaraceae). Koyama and
28
Khalifa and EL-Gohary [31] studied micro
morphological attributes like anatomical features of stem,
leaves and petioles to evaluate their significance in
differentiating the 9 Cleome spp. of Egypt. Lynne [32]
studied Cleomoideae and tried to explain their phylogeny
by using cladistic method. Farris [33] studied evolutionary
change for several characters in Cleome serrulata Pursh and
suggested that morphological characters had a greater
impact on fitness in wetter areas, while physiological
characters were more important in the drier areas. Mark et
al. [34] have studied different seed plants for their
phylogeny and reported that the polyphyletics that occurs
in capparidales is due to some members of capparaceae
along with Cleome. Erbar and Leins [35] studied floral
ontogeny of Cleome spinosa, Cleome violacea and Polanisia
dodecandra subsp. Trachysperma and concluded that the
evolutionary steps in the androecial development proceed
from Reseda via Capparis and Polanisia/Cleome to
Brassicaceae. Sanchez [36] tried to investigate phylogenetic
and morphological relationships within, South American
Cleome species. This study supported the monophyly of
Cleome and the recognition of three clades within it, which
are supported morphologically by seed and pollen
characters. In general, seed and, to a lesser extent, pollen
characters were found to be systematically useful within
Cleome species.
examined pollen morphology of 19 Cleome species from
Venezuela using scanning electron microscopy and
concluded that exine sculpturing has diagnostic value
within the genus and supports the classification of species
and there is no relationship between exine sculpturing and
pollination syndromes. Gamal [43] reported that pollen
grains of Cleome are tricolporate. Perveen and Qaiser [44]
investigated pollen morphology of 14 species belonging to
seven genera of the family Capparidaceae viz., Cadaba
Forssk., Capparis L., Cleome L., Dipterygium Decaisne,
Gynandropsis DC., Maerua Forssk by using light and
scanning electron microscopes. They concluded that
palynology is significantly helpful at the specific level.
Fagundez [45] worked on melitopalynology of Cleome
species comimg from the flooded islands with the help of
ligh and scanning electronic microscope. He for the first
time identified Cleome hassleriana pollen sample from
honey along with other plants also and studied importance
of each taxon in the production of honeys of these areas.
Page
dicotyledonous taxa new to Nepal flora. Sivarajan and Sunil
[29] for the first time reported Cleome spinosa Jacq., in wild
status from West Bengal, India (which is native of tropical
America). Panda and Paul [30] reported Cleome aspera
Koenig ex DC. as a new record for Flora of West Bengal.
Choshi [58] have studied developmental stages of pistil in
Cleome spinosa.
Rajendrudu et al. [59] have studied leaf phylotaxy in
Cleome gynandra L. Jelani et al. [60] have described foliar
dermotypes of the seven Indian species of Cleome, viz. C.
aspera Koen. ex DC., C. chelidonii L.f., C. felina L.f., C.
monophylla, L. C. gynandra L., C. tenella L.f. and C. viscosa L.
including epidermal cells, stomatal cells and trichome
complexes. Six trichome types viz., uniseriate capitate,
uniseriate cylindrical, biseriate capitate, multiseriate
capitate, multiseriate clavate and multiseriate conical hairs
have been observed. They prepared a key for identification
of the species studied. Idioblastic cell sacs have been
recorded in C. aspera, C. chelidonii, C. felina and C. tenella. It
was also reported by them that though, C. chelidonii is a
marshy plant, epidermal cells possess straight anticlinal
walls. Changes in the foliar traits of some common plants
including Cleome viscosa L. from polluted site were
observed by Saha et al. [61]. They have reported significant
variation in the palisade ratio and vein islet number in
Chromolaena odoratum, Cleome viscosa, Hyptis suaveolens
and Xanthium strumarium.
Raghavan [62] Studied complete life history of Cleome
chelidonii Linn. Weiss [63] studied domestically used plants
from East Africa which included Cleome strigosa and gave
its traditional use. Sharma [64] worked on systematic
position of 11 angiosperm genera [Atylosia, Centella,
Cleome, Glinus, Ludwigia, Malvastrum, Mukia, Pavonia,
Spergula, Trachyspermum and Zaleya] widely distributed in
India. Vanderpool and Estes [65] and Vanderpool et al. [66]
in their systematic investigation of Cleome lutia and Cleome
jonesii concluded that these two entities are conspecific,
each having n=17.
Rajagopal and Ramayya [67] studied anatomy of
Cleome aspera and found the occurrence of idioblastic cellsacs in the leaf epidermis which is significant character for
taxonomy of that plant. Iltis [68] worked on taxonomy of
Cleome multicaulis and described biogeography of this
species. He [69] studied monographic taxonomy and
evolution of Cleome gynandra. Bremer and Wanntorp [70]
made an attempt to classify Cleomoideae cladastically.
Brunel et al. [71] worked on taxonomy of Cleome and
prepared a floral key for identification. Anuradha et al. [72]
worked on chemotaxonomy of Cappareae and Cleomeae
and found that there are close ties among the members of
the two tribes. Subramanian and Susheela [73] studied
cytotaxonomy of 18 species coming under 6 genera of
Capparidaceae and for the first time recorded chromosome
number for some species. They concluded that the
autopolyploidy and allopolyploidy play an important role in
the origin and evolution of the species of South Indian
Capparidaceae. Ruiz [74] has given the taxanomic key for
identification of Cleome with three species and other five
genra from Capparaceae. Arbuzova and Nikitin [75] studied
taxonomy of Cleome and Cleomella-like fossil seeds from
the Palaeogene and Neogene of Russia and adjacent states
using scanning electron microscopy of the seed coat.
Khatoon and Perveen [76] studied Cleome heratensis Bunge
subsp. pakistanica and raised it to the species level as
Cleome pakistanica.
APG II system
Règne Plantae
Sous-règne Tracheobionta
Division Magnoliophyta
Classe Magnoliopsida
Sous-classe Dilleniidae
Ordre Capparales
Famille Capparaceae
Genre Cleome
Kingdom: Plantae
(unranked): Angiosperms
(unranked): Eudicots
(unranked): Rosids
Order: Brassicales
Family: Cleomaceae
Genus: Cleome L.
Classification System: APG III
Classification System: B &H
Regnum: Plantae
Cladus: Angiospermae
Cladus: Eudicots
Cladus: Core eudicots
Cladus: Rosids
Cladus: Eurosids II
Ordo: Brassicales
Familia: Cleomaceae
Genus: Cleome
Scientific classification
Kingdom :
Plantae
Division :
Angiosperms
Sub Division : Dicotyledonae
Class : Polypetalae
Series : Thalamiflorae
Order: Parietales
Family: Capparidaceae
Genera: Cleome
Page
Classification de Cronquist
29
Classification of Cleome in different system
Plant Sciences Feed Vol. 2 Issue 3
Murneek [85] studied andromonoecious reaction or
process in Cleome spinosa L. Eames and Wilson [86] studied
anatomy and floral morphology of Cleome spinosa. Brink
and Cooper [87] studied embryonic development in Cleome
chelidonii. Overbeek [88] studied weed control by different
synthetic chemicals. He reported that Cleome is controlled
by spraying 2, 4, D in agriculture field. Ramanujam and
Khatija [89] studied melittopalynology of Guntur District
Andhra Pradesh, India. A total of 66 pollen types referable
to 38 families including Cleome gynandra have been
recorded in these honey samples. Grzegorz and Maria [90]
investigated megafossils from the fluvial sediments
overlying the Tertiary lignites in the Bełchatów opencast
mine of Middle Poland and recorded some genera (Cleome,
Ternstroemites and Zingiberoideophyllum) which are new
for the Tertiary of Poland.
4. ECOLOGY
Cook [91] studied honey yield of Cleome integrifolia and
other two plants and found that Rocky Mountain bee plant
flourishes on the dry plains of Colorado, he had been quite
successful in growing it and geting much nectar in small
plots for years. Spring-sown seed will rarely germinate. So
in the fall of 1888 he sowed eight acres of Cleome but he
had great disappointment as the seeds did not germinate
well.
Henri [92] has recorded Cleome integrifolia as transient
weed. Menon and Kulkarni [93] have done ecological
studies in Cleome viscosa with respect to seed and seed
germination. Barker et al. [94] recorded the vegetation on
Plant Sciences Feed Vol. 2 Issue 3
Kassas and Zahran [100] reported Cleome droserifolia
community in El Galata and El Bahariya. According to Iltis
[101] centers of Cleome lanceolata are Paraguay and
Southwestern Brazil and NE Brazil. He [102] studied
ecological distribution of Cleome afrospina and its migration
from South America to Africa or vice versa. Cook [103]
reported Cleome ciliate and Cleome viscosa vegetation from
the Kainji reservoir site in Northern Nigeria. Leroy [104]
described 7 species of Cleome in which 3 species are
endemic to Madagascar.
Bruce [105] studied
phytogeography of sand dunes in great basin and Mojava
desert. He reported Cleome sparcifolia as indicator taxa of
all studied basins. Vegetation survey by Salama and Fayed
[106] revealed the following four community types in the
wadis Zilla spinosa - Aerva javanica, Pulicaria undulataSchouwia thebaica, Cleome arabica - Crotalaria aegyptiaca
and Acacia tortilis-Zygophyllum coccineum. Salama and
Fayed [107] studied phytosociology of thirty nine species
including Cleome droserifolia for comprising the vegetation
of the wadi using the Zurich Montpelliar technique. Ali et al.
[108] recorded one hundred and ten species, belonging to
35 families during survey of the Wadi Allaqi. They found
that among the recorded species, Cleome paradoxa,
Sesamum alatum, Gisekia pharnaceoides, Anticharis linearis
and Anticharis arabica are very rare in the Egyptian flora.
This study showed that vegetation distribution in the
30
Day by day there is increase in knowledge about genus
Cleome. Some common botanical features noted are as
follows: Gray [77] described Cleome integrifolia as
cultivated ornamental plant with very beautiful flowers.
Schaffner [78] observed long stipitate condition of the
gynoecium in some Cleome species which may cause
sterility in them. Bancroft [79] noted two species from
genus Cleome and showed an indication of tetrarchy in
hypocotyl. Frank [80] has reported that Cleome is a source
of surplus honey, so bees are attracted towards it. Rijven
[81] observed that glutamine at concentration of 400 ppm
stimulated the growth of embryos of Cleome. Acropetal
dehiscence with complete department of the valves as well
as basipetal incomplete dehiscence occur in the
cleomoideae [82]. Amelaxen and Arbeiter [83] indicated a
cytoplasmic origin for the oil as secretory product of
glandular hairs of Cleome spinosa. Thomas and Philips [84]
reported that leaf anatomy of Cleome tenuis indicated
operation of C3 metabolism.
the campsite members occupied by different fast-growing,
grazing-tolerant weeds like stoloniferous grass, Cynodon
dactylon, and the non-palatable, annual forbs, Cleome
tenella and Gisekia pharnaceoides. Ismail et al. [95] recorded
the occurrence of seeds belonging to 21 and 25 species in
the rubber and oil palm plantations respectively, with
Asystasia gangetica (L.) T. Anders., Cleome rutidosperma DC.,
Borreria alata DC. and Paspalum conjugatum Berg. being
the most abundant in both plantations and accounting for
more than 80% of the total weed seeds. Dickore and Nusser
[96] have reported Cleome as tropical weed in flora of
Nanga Parbat. Lawrence [97] identified Cleome serrulata
and other eleven species of other genera commonly
associated with corrals in Navajo. Merlee and Rekha [98]
studied Cleome viscosa for its autecology and provided
information regarding its distribution and abundance
which is helpful for its cultivation on a commercial scale.
Ghaderian and Baker [99] reported that Cleome heratensis
appears to be an indicator of ultramafics in Central Iran.
Populations of this plant cover quite extensive areas during
summer and autumn when there is no rainfall. This plant
contained low concentrations of all metals and thus it
possesses exclusion mechanisms to restrict excessive metal
uptake.
Page
3. BOTANY
Kers [117] studied population ecology of Cleome
angustifolia. The population ecology of Cleome droserifolia
(Forssk) Del. was studied by Hegazy et al. [118] in Egypt.
Costa et al. [119] described habitat, geographic distribution,
morphological variability and prepared illustrations of
different species of Cleome, for Brazil. They also prepared
key for these species.
Hammerton [120] reported Cleome spp. as weed and
described common methods and chemicals used to control
it. Wendy et al. [121] provided Banana mulch treatment
method for control of annual weed species such as
Spermacoce latifolia Aubl. and Cleome aculeate L. Cleome is
common plant found in tropical scrub habitat.
5. BIOTECHNOLOGY
Paigani And Romussi [122] have analysed seeds of
Cleome pungens using chromatography technique. They
isolated feruloyl choline chloride from the seeds using the
techniques like nuclear magnetic resonance, mass spectra,
Naseem and Jha [124] standardized in vitro protocol
for mass propagation of Cleome gynandra DC, using
thalamus, gynandrophore and root segments as explants on
Murashige and Skoog's medium varying the concentrations
of auxin and cytokinin. They observed that a high BA to
NAA ratio produced leathery leaves in culture besides shoot
differentiation. 2, 4-D was not suitable for organogenesis
and long term culture. Regenerants were successfully
transferred to soil. In vitro response of gynandrophore
culture was almost similar to that of thalamus explant.
Simoes et al. [125] have done biotechnological studies in
Cleome rosea. They studied the influence of cytokinins, 6benzyladenine (BA) and 6-furfurylaminopurine (kinetin)
added to the Murashige and Skoog medium (MS) on the
culture and reported plantlet regeneration by direct and
indirect organogenesis. Songsak and Lockwood [126]
established callus and suspension cultures from Cleome
chelidonii to produce glucosinolates.
6. CYTOLOGY
There are few reports on cytology of Cleome. Talyor
[127] studied chromosomes in Cleome spinosa during
mitosis. He recorded 32 chromosomes in the dividing cells
(2n=32). Áskell [128] worked on cytology of some
members of capparidaceae. According to him the
chromosomes number in some Cleome species is as follows.
Cleome gynandra L. n = 17, Cleome monophylla L. n = 11,
Cleome serrulata Pursh. n = 17, Cleome rutidosperma DC. n =
15, Cleome viscosa L. n = 10 and Cleome coluteoides Boiss. n
= 17. But according to Raghavan and Kamble [129]
chromosome number in Cleome gynandra L. is n = 10.
Renard et al. [130] have reported chromosome number for
three Cleome species, Cleome monophylla L. - 2n = 22, C.
schimperi Pax - 2n = 22 and C. gynandra 2n = 34. Koshy and
Mathew [131] worked on cytology of eight species of
Cleome, indigenous to South India and concluded that
chromosome data indicate that polyploidy and widespread
aneuploidy may have played significant role in speciation
and evolution of the genus. Wang et al. [132] worked on
cytology and micropropagation of Cleome spinosa Jacq. (2n
= 20), and also studied germination and the young sprout
growth of Cleome spinosa Jacq.
Farris [33] investigated the extent and adaptive
importance of genetically-based variation in plant water
relations in two populations of Cleome serrulata. He
collected seeds from maternal plants growing along the
moisture gradients and then grew under well-watered
31
Sen and Chawan [114] reported that Cleome viscosa
grows vigourously in spring season. Abdul [115] reported
that Cleome arabica, an annual species is grown only in
winter season. Singh et al. [116] studied weed competition
in green gram (Vigna radiata) and black gram (Vigna
mungo)field and reported the following species during the
monsoon seasons Echinochloa colonum, Dactyloctenium
aegyptium, Eleusine indica, Digitaria sanguinalis, Celosia
argentea, Phyllanthus niruri, Cleome viscosa and Cyperus
rotundus.
uv spectrum and IR spectrum. Koch et al. [123] proposed
that genus Cleome is closest relative of brassicaceae on the
basis of molecular biology.
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studied area was largely dictated by environmental
physiogeographic gradients that control the water
availability in an extremely arid desert. Reddy et al. [109]
reported new naturalized Cardamine trichocarpa Hochst. ex
A. Rich. and Cleome rutidosperma DC. in Andhra Pradesh,
India. Nagar [110] reported Cleome scaposa DC.a rare
species for Saurashtra. Galán de Mera et al. [111] for the
first time reported Cleome violacea L., Puccinellia frigida
(Phil.) I. M. Johnst., Sisymbrium altissimum L. and Solanum
nitidibaccatum Bitter from Peru. Waterhouse [112] has
given new distribution records for the serious tropical
weeds Chromolaena odorata (L.) R.M. King & H. Rob.
(Asteraceae), Mikania micrantha Kunth (Asteraceae),
Cleome rutidosperma DC…. in northern Australia, Papua
New Guinea and Papua (Indonesia). Barua et al. [113] have
described bioecological activities of Leptosia nina var nina
Fabr, a common Pierid butterfly on Cleome viscosa. The
ecological observations were carried out by them in the
field to determine the status and distribution, habits and
habitat, feeding, courtship, mating and egg-laying
behaviour.
Plant Sciences Feed Vol. 2 Issue 3
7. BIOCHEMISTRY
Biochemistry of number of Cleome species has been
studied extensively. Thirty eight species of Capparidaceae
including Cleome had been analyzed for their content of
isothiocyanate-producing glucosides for taxonomic
significance of species and possible biogenesis of the
glucosides [136]. Chauhan and Srivastava [137] have
worked on some phytochemical aspects of the roots of
Cleome viscosa. Rao [138] determined some characteristics
of seed oil from Cleome viscosa and found that the seeds
contain 26% oil. This oil is composed of 10.6%palmitic,
4.9% stearic, 14.4% oleic and 68.6% linoleic acids. Singh
[139] has studied leaf protines of Cleome viscosa. Kumar et
al. [140] have studied effect of isoproturon on leaf cell
membrane permeability of Cleome viscosa. Cleomiscosin D,
a minor coumarino-lignan of the seeds of Cleome viscosa,
has been proved to be regioisomer of cleomiscosin C [141],
and developed a method for degradation of coumarinolignans.
Mnzava [142] studied biochemical properties (Amino
acid analysis, iodine and saponification numbers, crude
protein, lipid, oleic and linoleic acids of the total fatty acids)
of seeds of Cleome gynandra. Hussein et al. [143] have
Plant Sciences Feed Vol. 2 Issue 3
Different workers have isolated different compounds
from different Cleome species e.g. Kaempferide 3glucuronide from the roots [145]; new naringenin
glycoside [146]; three new coumarino-lignoids from the
seeds [147], which posses liver-protective properties
(cleomiscosins A, B and C); stigmasta-5,24(28)-diene-3β-Oα-L-rhamnoside [148] and two new unsaturated cembrane
acids [149] from Cleome viscosa. Cleosandrin from Cleome
icosandrica [150]; Cleomeprenols from Cleome spinosa L.
which were identified as nonaprenol, decaprenol and
undecaprenol [151]. Viqar and Khisal [152] have isolated
cabralealactone and ursolic acid and new trinortriterpenoid
Cleome
dilactone,
deacetoxybrachycarpone
from
brachycarpa by spectroscopic analysis. Ahmad and Alvi
[153] have isolated a cabralealactone, ursolic acid and new
trinortriterpenoid dilactone, deacetoxy-brachycarpone
from Cleome brachycarpa and determined its structure.
Ahmad et al. [154] isolated a new triterpenoid
cleocarbpone from Cleome brachycarpa.
Sharaf et al. [155] examined aerial parts of four Cleome
species (Cleome droserifolia, C. amplyocarpa, C. brachycarpa
and C. chrysantha) for their surface flavonoids content. Ten
methylated flavonoids were isolated and identified as
isokaempferide, 5,7,4'-trihydroxy-3,3'-dimethyoxyflavone,
Jaceosidin, penduletin, axillarin, 5,7,4'-trihydroxy-6,3',5'trimethoxyflavone,
chrysosplenetin,
5,3'-dihydroxy3,6,7,4',5'-pentamethoxyflavone, 5,4'-dihydroxy-3,6,7,8,3'pentamethoxyflavone
and 5-hydroxy-3,6,7,3',4',5'hexamethoxyflavone. Two triterpenes of the dammarane
type compounds from aerial parts of Cleome africana were
isolated and their structure was elucidated by Tsichritzis
[156] using high field NMR spectroscopy.
Hussein et al. [157] isolated and identified some
sesquiterpenes from Cleome droserifolia. Harraz et al. [158]
have isolated 6 dormane terpenes from Cleome
ambylocarpa. Ndungu et al. [159] isolated the essential oil
from Cleome monophylla. The identified constituents of this
oil were evaluated and of these 14 compounds were
identified by GC, GC-MS and coinjection with authentic
samples. They have discussed the potential of C. monophylla
against tick attack.
Sharaf et al. [160] isolated and identified thirteen
flavonoid glycosides from four Cleome and three Capparis
species. Qin et al. [161] isolated and elucidated new
32
Hegazy et al. [118] investigated the autotoxic effects of
Anastatica hierochuntica and possible effects on Cleome
droserifoliaand found that the mitotic index was reduced by
55% in C. droserifolia at the 8% level of the A. hierochuntica
extract concentration. Naseem and Jha [133] cultured callus
derived shoot buds from younger leaves of the growing
shoot of Cleome viscosa on Murashige and Skoog medium
fortified with various combinations of 1-Naphthalene acetic
acid (NAA) and 6-Benzylamino pure (BA). Rooting of shoots
was obtained by using Indol-3-butyric acid in the medium
and regenerated plantlets were subsequently transferred to
the soil. Susana and Michael [134] attempted gene
sequencing in Cleome hassleriana using atpB and rbcL.
Claudia et al. [135] worked on cytogenetics and pigement
composition of Cleome rosea. They cultured calluses using
leaf and stem explant on MS medium supplemented with
different concentrations of 2,4-dichlorophenoxyacetic acid
(2,4-D) and from that eleven anthocyanins were obtained
by using high performance liquid chromatography coupled
to diode array detector and electrospray ionization mass
spectrometry (HPLC-DAD/ESIMS).
worked on sesquiterpenes from Cleome droserifolia.
Songsak and Lockwood [144] reported that Cleome
chelidonii and Cleome viscosa contain glucocapparin and
glucocleomin, while Cleome gynandra has only
glucocapparin.
Page
conditions in the greenhouse. By his exprement he
suggested that natural selection had acted on this character
during one or more previous generations. It appears that
slight variations in the physiological genotype can
significantly affect overall fitness in C. serrulata.
Seif et al. [168] have reported some flavonoids from
Cleome droserifolia which were identified as kaempferol-3O-glucoside, rutin, kaempferol and luteolin-7-O-glucoside.
Yang et al. [169] reported five flavonoids from aerial parts
of Cleome droserifolia (Forssk.) Del. Mohamed et al. [170]
investigated ten methylated surface flavonoids from four
Cleome species. Narendhirakannan et al. [171] studied the
anti-arthritic nature of Cleome gynandra L. against Freund’s
complete adjuvant induced arthritis in rats and reported
the presence of many biologically active phyto chemicals
such as triterpenes, tannins, anthroquinones, flavonoids,
saponins, steroids, resins, lectins, glycosides, sugars,
phenolic compounds, and alkaloids in the extract of C.
gynandra and these compounds might be responsible for
the anti-arthritic properties.
Leo et al. [172] synthesized Cleomeolide, the
structurally unique diterpene lactone constituent from
Cleome viscosa. Fathalla et al. [173] obtained four new and
two known dammarane-type triterpenes from Cleome
amblyocarpa. Hidekazu et al. [174] obtained eighteen
dammarane-type triterpenes from Cleome africana. Twelve
of these were novel compounds. Nagaya et al. [175]
separated eighteen triterpene compounds from Cleome
africana, in which twelve were novel.
Preliminary work by Zhang et al. [176] revealed that
dry seeds of Cleome spinosa evolve at least 24 kinds of
volatile compounds into the ambient atmosphere during
Ndungu et al. [178] identified three constituents from
the essential oil of Cleome hirta (phytol, (+)-cedrol, noctacosane) and evaluated against the livestock tick,
repellency and discussed potential of C. hirta in livestock
tick and maize weevil control. Monica et al. [179] identified
one monoacylated and four diacylated cyanidin 3sophoroside-5-glucosides as the main anthocyanins in
flowers of Cleome hassleriana Queen Line.
Sawaya et al. [180] have worked on chemical
composition and nutritional quality of Cleome dolichostyla.
Louda [181] studied chemical changes in Cleome serrulata.
He found that methylglucosinolate concentrations
decreased significantly due to insect damage. Khafagi [182]
developed
heterotrophic
callus
cultures
and
photomixotrophic cultures from whole seedlings of Cleome
droserifolia and studied the effect of light and dark
conditions on them and found that the heterotrophic callus
cultures excreted allelochemicals (autotoxic) which
inhibited callus induction and development. Mirza et al.
[183] studied essential oil of Cleome iberica DC. and found
that it has 26 components. Constance et al. [184] studied
anthocyanin pigmentation patten in petals of cultivated
Cleome hassleriana Chodat and wild species, Cleome
serrulata Pursh. (Rocky Mountain bee flower) and their
relation with three genera of the Brassicaceae.
8. PHYSIOLOGY
Physiological studies in Cleome species are very rare.
Zeevaart [185] studied the effect of growth retardants on
plant growth and development in many species. He
observed that application of amo (2,12), CCC and phoston D
caused delayed flowering in Cleome species. Vyas and Garg
[186] have studied interaction of GA and light on the
germination and growth of seedlings of Cleome viscosa. de
33
Different diterpene derivatives are isolated from
Cleome. Mahato et al. [164] have isolated new diterpene
lactone from Cleome isosandrica. Burke et al. [165] isolated
bicyclic diterpene cleomeolide from Cleome viscosa L. and
established its stereo-structure by chemical, spectral and Xray crystallography techniques. Jente et al. [166] isolated a
new macrocyclic diterpene (3E,7E,11E)-20-oxocembra3,7,11,15-tetraen-19-oic acid (cleomaldeic acid), from
Cleome viscosa. Mahato [167] isolated Cleomeolide, a
diterpene lactone from Cleome icosandra and reported that
it may be used for therapeutic intervention in a wide range
of diseases.
storage periods. The abundant production of butane was
found in two kinds of tropical plants, Cleome spinosa Jacq.
and Cyperus alternifolius L. The fact that the amount of
evolved volatiles increases with increasing period or
temperature of seed storage and suggests that these
volatiles are produced metabolically even in dry seeds.
They have found that the concentration of butane is high in
Cleome spinosa.. McLean et al. [177] examined for the
presence of betaines and other quaternary ammonium
compounds in 55 species and varieties of Capparaceae
distributed in 17 genera. It was found that prolinebetaine
and/or 3-hydroxyprolinebetaine were detected in all the
species of Crataeva, Ritchlea, Maerua, Boscia, Capparis,
Cladostemon, Cadaba, Thilachium, Morisonia and
Steriphoma, whereas glycinebetaine was only betaine
found in Cleome species.
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trinortriterpenoid, 1-epibrachyacarpone from Cleome
chrysantha. Songsak and Lockwood [126] have isolated 2
volatile glucosinolate hydrolysis compounds in Cleome
chellidonii. Tandon et al. [162] studied and isolated
cleomiscosins A, B and C from the seeds of Cleome viscosa.
Chattopadhyay et al. [163] have isolated the optically active
nevirapine, a natural analogue of the previously designed
and synthesized optically inactive nevirapine, a nonnucleoside inhibitor of HIV-1 reverse transcriptase from
the seeds of Cleome viscosa.
Plant Sciences Feed Vol. 2 Issue 3
Rajendrudu et al. [191] studied growth of different
plants (ecotypes) of Cleome gynandra L. that exhibits
diaheliotropic leaf movements. The plants were grown at
full (HI) and 40% (LI) natural irradiance. Sailaja et al. [192]
studied
laser-induced
F-685/F-720
chlorophyll
fluorescence of intact leaves in solar tracking different
plants including Cleome gynandra. It was found that the
plant exhibited remarkable diurnal constancy in contrast
and suggested that the leaves of diaheliotropic plants
maximise light-use efficiency throughout the day and avoid
the hazard of midday depression of photosynthesis.
Naidu et al. [193] have studied photosynthetic pathway
in some weeds including Cleome gynandra and C. speciosa.
Rajendrudu and Rama [194] could find some differences in
the levels of dark respiration between C3 and C4 species
like Cleome gynandra, L. C4 , Cleome rutidosperma, DC. C3,
Cleome monophylla, L. C3 and Cleome viscosa, L. C3. Higher
rates of dark respiration and photosynthetic CO2 uptake
found in C4 plants and in some C3 species may form the
basis for the rapid plant growth and biomass production
per unit time in these species. They also studied
carboxylating enzymes in the leaves of Cleome gynandra.
They concluded that, the plant shows Kranz-type leaf
Plant Sciences Feed Vol. 2 Issue 3
Dutt et al. [199] worked on distribution pattern of free
amino acids in Moringa concanensis, M. oleifera, Cleome
chelidonii, C. gigantea, C. gynandra, C. monophylla, C. viscosa
and Crataeva nurvula for systematic position of Moringa
and concluded that Moringaceae shows almost no affinity
to Capparaceae. Mnzava [142] studied the seeds of
Gynandropsis gynandra L. for their lipids, amino acids and
proteins composition. Meyers [200] compaired Cleome
serrulata and wheat for their protein content and
concluded that protein content of Cleome serrulata is two
times higher than that of wheat plants. Rathore and Meena
[201] have shown that leaves of Cleome viscosa contain
29.9% crude protein.
Selloum et al. [202] studied antioxidative activity of
Cleome arabica L. leaf extract by using superoxide anion
radical generating systems. Narendhirakannan et al. [171]
tried to investigate the possible anti-oxidant potential of
Cleome gynandra leaf extract on experimental rats and
concluded that presence of biologically active ingredients
and vital trace elements in the leaves readily account for
34
Stephan [188] showed that pollen grains of Cleome
lutea can be germinated upto 57% on 15 % sucrose
medium. He also found an inhibition of pollen germination
due to UVB radiation in number of plants including this
species. Ochuodho and Modi [189] have studied
temperature and light requirement for seed germination in
Cleome gynandra. They studied chilling, scarification,
hydration and germination in the presence of KNO3 or GA
(3) on the germination of seeds. They concluded that
germination of seeds was improved by treatment with GA
(3) and recommended that the germination should be
performed under conditions of darkness and either
alternating 20-300C. Boonsong et al. [190] investigated
influence of seed maturity, seed storage and germination
pre-treatments on seed germination of Cleome gynandra.
They used different treatments (various levels of GA3,
KNO3, leaching, pre-chilling, soaking and pre-heating at
different temperatures) and reported that pre-heating at
40 °C for 1–5 days period was the most effective method for
dormancy breaking. Rao et al. [25] have studied the
allelopathic effect of aqueous extracts of Cleome viscosa on
the germination and early seedling growth of bajra.
anatomy and there was higher activity of PEP carboxylase
in the whole leaf extracts than the other Cleome species.
Brown et al. [195] proposed that Cleome is very closely
related genus containing C-4 species to the C-3 model
Arabidopsis and may be used to accelerate our progress in
elucidating the genetic basis of C-4 photosynthesis. Sawaya
et al. [180] analysed seeds of Cleome dolichostyla for
mineral element contents, amino acid composition and in
vitro protein digestibility and calculated protein efficiency
ratio and concluded that seeds were rich (dry wt basis) in
oil (32.1%), protein (24.6%) and fiber (17.8%). The
amount of various mineral elements (mg/100 g) was Ca,
1970; P, 493; Mg, 127; Na, 35; K, 465; Fe, 71.97; Zn, 2.25;
Cu, 0.44 and Mn, 1.45. Aspartic acid, glutamic acid, glycine,
arginine and histidine were the major amino acids in C.
dolichostyla seed. Badri et al. [196] determined the mineral
composition (Ca, Mg, K, Na, Fe, Al, Mn, Co, Ni, Cu and Zn) of
Senna alexandrina and Cleome droserifolia in the Eastern
Desert of Egypt. It was found that the concentration of Fe,
Al, Mn, Co, Ni, Na and Si in the leaves of Cleome was always
higher than that in the leaves of Senna. Edeoga et al. [197]
determined mineral and nutrient components like crude
protein, crude fibre, carbohydrates, crude lipid, ash and
food energy of leaves and stems of Cleome rutidosperma,
along with other nine commonly used medicinal plants of
Nigeria and suggested that these medicinal plants could
potentially be used as raw materials in drug formulation.
Lottermoser et al. [198] reported that the uptake of Cd, Pb
and Zn by Cleome viscosa increases linearly with DTPAextractable soil metal concentrations.
Page
Jong and Bruinsma [187] reported that application of
ethylene and ascorbic acid resulted in inhibition of
gynoecium in Cleome iberidella. Auxin transport inhibitor
TIBA had no effect on corolla elongation while there was
growth promotion by gibberellin.
9. IMPORTANCE OF CLEOME SPECIES
Some of the Cleome species are widely used as food
medicinal plants. Slosson [206]
reported Cleome
speciosissima is cultivated for bee food as well as for
flowers. Walter [207] reported that Cleome integrifolia
leaves boiled with green corn can be used as food.
Krochmal et al. [208] studied many plants and reported
that some Cleome species are eaten by Indian people as
vegetable and obtain black dye from Cleome serrulata after
boiling it in water. Odhav et al. [209] collected preliminary
nutritional data for traditional leafy vegetables in Kwa ZuluNatal, South Africa. Twenty vegetables were studied for
their content of mineral elements and antioxidant levels
and all including Cleome monophylla recommended for
future commercial cultivation.
Different Cleome species show different medicinal
properties. Shabana et al. [210] tested molluscicidal and
cercaricidal activities of fifty-eight plants from 22 families
and found lower molluscicidal effectiveness shown by
extracts of Panicum turgidum, Calligonum comosum, Cleome
amblyocarpa, Cornulaca monacantha, Silene villosa, Jasonia
montana and Achillea fragrantissima. Saxena et al. [211]
tested 15 plants; four plant extracts showed anti-juvenile
hormone against mosquitoes in the acetone extracts of
Ageratum conyzoides, Cleome icosandra, Tagetes erectes and
Tridax procumbens. They observed significant anti-juvenile
property against mosquitoes only in Ageratum, Cleome and
Tridax extracts. Loss of fecundity was observed in the
treated mosquitoes but no sterilant effects could be
recorded. Adults, obtained from larvae exposed to the plant
extracts produced significantly shorter egg-rafts than in
Gardiner and Brace [220] reported medicinal
properties of Cleome gynandra for relieving pain, curing
skin diseases like lepracy and earache. Bedi [221] noted
that leaf juice of Cleome viscosa was used to remove pus
from wound and leaf juice and oil from seeds of Cleome
gynandra were used to cure skin diseases. Mpuchane and
Gashe [222] determined antibiotic sensitivity of Klebsiella
isolates for Corchorus olitorius and Cleome gynandra.
Shackleton et al. [223] studied use and trading of Cleome
gynandra in South Africa and reported that generally 82%
people use Cleome gynandra in their diet in the Central
Lowveld Savanna Region, and in winter, Cleome gynandra
(usually dried) and Momordica balsamina were the
principal herbs widely sold. Samy et al. [224] studied
antibacterial activity of 16 different ethnomedicinal plants
along with Cleome gynandra and Cleome viscosa. These
Cleome species were tested against three gram positive and
seven gram negative bacteria by the filter paper disc
diffusion method. It was found that the extract of these
species significantly controls the growth of all bacteria.
Zemede and Mesfin [225] mentioned that Cleome gynandra
35
Kumar et al. [204] have worked on differential
performance of Cleome gynandra and C. specoisa under
water stress and their recovery conditions. When Cleome
serrulata, growing at two sites (dry and wet sites) was
studied for comparision, Farris [205] found that
morphological and growth characters were important for
its fitness in mesic site, while physiological characters were
more important in the dry site.
control. Smyth [212] studied anthelmintic, antipyretic and
tonic properties of Cleome serrulata. Ganesan [213] studied
antifungal properties of 30 plants against Drechslera oryzae
and reported that the aqueous leaf extracts of Cleome
aspera could effectively inhibit germ tube elongation.
Perumalsamy and Raja [214]
studied antibacterial
properties of aqueous extracts of some selected weeds
including Cleome species. Ndungu et al. [178] studied
potential of essential oil of Cleome hirta and reported that
three identified constituents (phytol, (+)-cedrol and noctacosane) were evaluated against the livestock tick, and
maize weevil. Lazzeri and Manici [215] have studied
fungitoxic activity of Cleome hassleriana. Stephan et al.
[216] have studied nematocidal activity of some Cleome
species. They have reported toxicity of crude extract of
different plants including Cleome against egg-masses of
Meloidogyne javanica, a root-knot nematode and found that
pre-planting application of Cleome extracts resulted in
significant reduction in root-gall index and improved plant
growth (dry shoot and root weights). Mothana et al. [217]
investigated Cleome socotrana as well as other 24 different
plant species, for their antiviral activity. Nagarajan et al.
[218] studied activity of petroleum ether and benzene
extracts of Cleome felina on alloxan diabetic rats and
concluded that this plant extract has antidiabetic and
antihyperlipemic properties. Sharma et al. [219]
synthesized first time six novel cleomiscosin A and studied
potent anti-inflammatory activity using primary
macrophages cell culture bioassay system.
Page
free radical scavenging property of C. gynandra. Djeridane
et al. [203] screened 18 Algerian medicinal plants for their
phenolic contents and radical scavenging activities and
reported that the phenolic extract of Cleome arabica was
the most effective. Compared to six other standard
antioxidants (ascorbic acid, α-tocopherol, Trolox, (+)
catechin, p-coumaric acid and gallic acid) the isolated
compound was found to be significantly more active in the
radical scavenging assay using 2, 2-diphenyl-1picrylhydrazyl (DPPH).
Plant Sciences Feed Vol. 2 Issue 3
Plant Sciences Feed Vol. 2 Issue 3
Bose et al. [243] have studied antimicrobial activity,
analgesic, anti-inflammatory and antipyretic activity of the
ethanolic extracts of Cleome rutidosperma.
Bellakhdar [244] have reported that in the Sahara and
Dra region, fruits and leaves, mixed with Cleome arabica L.
sub sp. Amblyocarpa and olive oil are used as antiinflammatory ointments. Bouriche et al. [245] found that
Cleome arabica contains higher amount of flavonoids
(19%) due to which it posses high anti-inflammatory
activity. The effects of Cleome arabica leaf extract, rutin and
quercetin on soybean lipoxygenase (Lox) activity was
investigated by Bouriche et al. [246]. It was found that the
extract was beneficial for the treatment of inflammatory
conditions, particularly those characterised by excessive
leukotriene generation. Ismail et al. [247] studied
antiinflammatory property and flavanoids of Cleome
arabica leaves and twigs.
Yaniv et al. [248] have done ethnobotanical survey for
the medicinal plants of Israel, 16 species were found to be
used for hypoglycaemic treatments, Cleome droserifolia is
one of those. Hegazy and Fadl-Allah [249] studied the effect
of Cleome droserifolia shoot extract on its seed germination
36
Polasa and Rukmini [231] tested eight unconventional
oils by the Ames mutagenicity assay and recorded no
mutagenic activity of Cleome viscosa oil. Sebastian and
Bhandari [232] have carried out ethnobotanical survey
from Rajasthan and reported that certain plants such as
Fumaria indica, Brassica juncea, Cleome viscosa, Portulaca
oleraceae, Bauhinia variegata are used as vegetable. Khare
et al. [233] collected fifty plants for the study of their
efficacy against stored grain insect pests. Four ornamental
plants and two wild plants Cleome viscosa and
Boenninghausenia albiflora were found naturally infested
by Lasioderma serricorne. Maikhuri et al. [234] described
the agronomy, yield, cost-benefit analysis, uses, and
ethnobotany of Cleome viscosa and suggested that
systematic efforts must be made to promote its cultivation
on a larger scale in the degraded and in marginal
agricultural lands where traditional crops grow with
difficulty. Devi et al. [235] studied anti-diarrheal potential
of the entire Cleome viscosa L. plant on rats.
Bhamarapravati et al. [236] studied gastroprotective
properties of methanol extracts of Cleome viscosa (leaf)
plants. Devi et al. [237] studied anti-inflammatory potential
of methanol extracts of Cleome viscosa against carrageenin,
histamine and dextran induced rat paw oedema. They also
studied antipyretic activity of a methanol extract of this
plant on normal body temperature and yeast-induced
pyrexia in albino rats. They showed that there was
significant reduction in normal body temperature and
yeast-provoked elevated temperature. Oladele and Abatan
[238] studied toxic effects of crude aqueous extracts of the
leaves of Cleome viscosa, on serum biochemical parameters
and histopathology in albino rats and reported that there
was significant increase in the blood urea nitrogen in the
rats and they concluded that the effect of Cleome viscosa is
nephrotoxic. Parimaladevi et al. [239] studied analgesic
activity of methanol extract of Cleome viscosa in mice, and
reported promising activity in all the tests. Vijayan et al.
[240] have investigated antifungal activity of Cleome
viscosa. A study on Cleome viscosa by Williams et al. [241]
revealed the presence of secretory glandular, club-cylinder
and cylinder shaped trichomes on the leaves and stems of C.
viscosa were extracted with hexane and the extract was
evaluated for different biological activities like antibacterial, anti-fungal, insecticidal and nematicidal activity.
Sudhakar et al. [242] tested antimicrobial activity of
ethanolic extracts of the leaves and flowers of Cleome
viscosa against Escherichia coli, Proteus vulgaris and
Pseudomonas aeruginosa.
Page
is cultivated alongside other vegetables and black dye
obtained from Cleome serrulata is two times higher than
that from wheat plants. Hebbar et al. [226] conducted
ethnomedicine survey of the Dharwad district of Karnataka
in southern India. They recorded 35 plants belonging to 26
families for their medicinal properties. They reported that
Cleome gynandra is used to treat tooth ache.
Narendhirakannan et al. [171] worked on medicinal
properties of Cleome gynandra L., which has traditionally
been used for the treatment of rheumatic and other
inflammatory conditions. Here they worked on checking
significant anti-inflammatory activity in adjuvant-induced
arthritic rats and demonstrated that the plant extract has
no harmful effect and exerts in vivo anti-inflammatory
properties against adjuvant induced arthritis. Modern Hopi
people served Cleome gynandra L as an important
starvation plant [21]. The antibacterial activities of Cleome
gynandra were studied by Vijayakumar et al. [227] against
Escherichia coli, Proteus vulgaris and Enterobacter faecalis.
Samuel and Brian [228] reported use of Cleome gynandra as
inter crop helpful for significant reduction of red spider
mite (Tetranychus urticae Koch) in greenhouse rose
production. Upadhyay et al. [229] isolated essential oils
from Cleome gynandra and studied for their insecticidal,
oviposition inhibitory and repellent activity against pulse
beetle and concludeded that these essential oils could be
used in the control of storage pests and are quite safe. Bala
et al. [230] studied anticancer activity of methanolic extract
of Cleome gynandra in swiss albino mice and showed that
plant has potent dose dependent anticancer activity.
10. PATHOLOGY
Species like Cleome spinosa are susceptible to different
pathogens like Puccinia vexans, P. tosta, P. subnitens,
tobacco budworm, Peronospora parasitica, cabbage white
butterfly, Erysiphe cruciferarum, Aphis gossypii Glover and
Myzus persicae aphids ([257] [258]; [259]; [260]; [261];
[262]; [263] and [264]). Puccinia subnitens also grows on
Cleome serrulata [259]. Cabbage white butterfly insect
breeds on weeds like Cleome viscosa and Cleome gynandra
and parasite complex of cabbage budworm is richer and
more consistent on Cleome species [265]. Benrey et al.
[266] investigated the influence of four host plant species,
including Cleome spinosa (spider flower), on two
Ellis and Halsted [267] and Kellerman [268] reported
new fungal species Cercospora cleomis on Cleome pungens,
Cercospora conspicua on Cleome gynandra and Eeidium
cleomis on Cleome integrifolia [269].
Raman and Sanjayan [270] studied the host plant and
pathogen relationships in terms of the comparative growth
rate, survival percentage, reproductive efficiency and
population dynamics and indicated that the most preferred
host plant for mirid, Cyrtopeltis tenuis are Lycopersicon
esculentum Mill. (Solanaceae), followed by Luffa cylindrica
Roxb. (Cucurbitaceae), Cleome viscosa L. and Gynandropsis
pentaphylla DC. Different Cleome species are recorded as
host plant for many pathogens such as Cleome gynandra as
host plant for Liriomyza hawaiiensis [271]; Cleome
graveolens Raf. for crown gall disease [272]; Cleome viscosa
for powdery mildew [273]; Cleome viscosa, C. spinosa for
PRSV melon viruse and C. viscosa for WMV-2 and ZYMV
melon viruses [274] and also for Albugo cruciferarum, the
white rust of mustard [275]. Zhang and Wang [276]
reported Albugo capparidis on Cleome gynandra L. and C.
viscosa L.
Cleome rutidosperma is infected by Appias libythea
[277] and cabbage webworm [278]. The egg to adult
development of diamondback moth, Plutella xylostella (L.)
was found fastest on Cleome hassleriana [279]. Getachew et
al. [280] reported unwanted and health problematic effect
due to Cleome gallensis plants.
Mamula [281] worked on of transmission of
belladonna mottle virus (BMV) to Cleome spinosa plants.
Bohart and Smith [282] studied plant insect interaction
between Ammoplanops and Cleome species. Field studies
were conducted by Mehra et al. [283] on weed control in
irrigated groundnut and recorded that Fluchloralin,
pendimethalin and oxadiazon herbicide treatments were
found effective against, Cleome viscosa and Diodia teres.
Nyambo [284] studied insect pest of cotton in Western
Tanzania and investigated the role of natural enemies in
regulating the larvae populations of the pest in the mixed
cropping system using Cleome sp. They observed that the
diseases (viral and bacterial) and parasitism were
identified as important mortality factors of the larvae
populations but neither prevented the pest population from
causing economic damage on the crops.
37
Shahina et al. [251] reported that Cleome rupicola
extract can be applied as eye-drops. Hawley [252] prepared
black carbon paint from Cleome. Saboor et al. [253] have
tested Cleome dolichostyla seed oil extract for iodine
number, saponification number, Hehner value, ReichertMeissl number and refractive index and reported its
potential as an edible oil for human. Shackleton [254]
examined use and commercial value of wild edible herbs in
South Africa which include Amaranthus, Bidens,
Chenopodium, Cleome, Corchorus and Momordica. Juan and
Gabriele [255] Studied herbal mixtures in the traditional
medicine of Eastern Cuba and created 199 formulae by
using one hundred seventy plant species including Cleome
species. Claudia et al. [256] compared methanolic extracts
of Cleome rosea, collected from natural habitat and from in
vitro propagated plants. They also analysed different in
vitro biological assays and reported that C. rosea presents
medicinal potential and that the acclimatization process
reduces the plant toxicity both to plasmid DNA and to J774
cells.
components of the host selection process in Cotesia
glomerata (L.), namely, attraction and host acceptance and
concluded that phytochemistry mediates host selection
more by influencing parasitoid attraction than it does by
affecting host acceptance.
Page
and seedling growth. Cleome droserifolia was found
autotoxic. A total of 20 fungal species belonging to 10
genera were found by Badran and Aly [250] to be
associated with all stages of Culex pipiens. The water extract
of both Artemesia cina and Cleome droserifolia showed an
inhibitory effect on the protein content and growth of some
selected isolates. Hegazy and Fadl-Allah [249] examined the
effect of different extracts of Cleome droserifolia on its seed
germination and seedling growth, and concluded that
Cleome droserifolia is autotoxic. They tested allelopathic
effects of Cleome droserifolia on Penicillium chrysogenum
and P. funiculosum and found that these fungi are most
sensitive. Badri et al. [196] have studied accumulation of
metals in Cleome droserifolia. Khafagi [181] studied
anthelminthic and antibacterial activity of ethanolic
extracts of twelve plant species including Cleome
droserifolia (Forssk.) Del. against six bacterial strains.
Plant Sciences Feed Vol. 2 Issue 3
As per mineral analysis Cleome species have great
tolerance capacity for any kind of environmental stress and
also indicates that these species may act as antioxidants. On
the basis of GCMS analysis seed oil from five different
Cleome species shows much more similarity. Some
compounds found common in all studied species at
measurable concentrations may be taxonomically
important criteria for family Cleomaceae or genus Cleome.
While, some compounds are specific and are found only in
single species. This character is also helpful for the study of
variation among the species. SEM studies in Cleome species
have shown that seeds of every Cleome species have their
own ornamentation characteristics which will be helpful in
identification of plant species on the basis of seed
ornamentation.
The review of the researches will provide guidelines
for understanding the value of the Cleome species and this
will be helpful for further researches with spider flower
genus Cleome.
[8]
[9]
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