
- •Instance , a ntioxidant s a re biologically produced as
- •Xanthones, flavonol and proanthocyanidins in l eaves
- •In c. Sura ttensis flower [4]. Lutein prot ects pho to-induc ed free radical damage in plant t issues in 2 ways:
- •Is the first report on the inhibitio n activity of most plant
- •Inhibit the growth of a broad spectrum of bacteria
- •In c. Pul c he rr ima [20,21,42,43]. Ph ytochemical com-pounds in c. Pulcherrima tha t posse sse d an timicrobial
- •100 G of dry l . Leucocep hal aleaves, 0.53 g/100 g I n
Is the first report on the inhibitio n activity of most plant
extracts against MRSA.
As phyt ochemicals o f ten play a n i mpor tant role in
plan t defe nce aga inst prey, mic roo rganis m, stress as well
as inters pecies protec tions, th ese plant comp onents have
been used as drugs for millennia. Hence, phytochemicals
scre en in g s erv es a s t he ini t ial s tep in p redic t in g t he
types of potential active compounds from plants.
The presences of flavonoids [32], triterpenoid saponins
[33] and t annins [34] in A. auriculiformis have been
re p or te d. Goo d D PP H fr ee ra di ca l s ca ven g in g ac t iv i ty o f
A. a uriculiformisis not only a ttributed to the presence
o f t a nn i n s, b ut a l so l e uc o an t ho c ya n i di n s ( l e uc o d el p h i ni -dins and l eucocyanidins) which are present abundantly
in the plant. This is because of the h ydroxylation at 4 ’
o r t ho p o s i t i o n o f l e u co an t h o c ya n i d i ns t h at c o u l d ch a n g e
DPP H radi cal to no n- radi cal DPP H-H [35] . Be sid es , tw o
acy la ted b isglyc oside s aponins, a caciaside A and B iso-lated fr om A . au r ic ul if o rm is, we r e fo un d to ex hi bi t an ti -bacterial a nd antifungal ac tivi ty. Mandal e t al. [36]
foundthatmixture ofthesetwo saponinsareableto
inhibit c onidial germinatio n of Aspergillus o chraceous
and Curvularia lunata at 300 μg/mL while the bacterici-dal co n cen tration of the mixture agai ns t Ba cillus mega-teri um , Sa lmonella ty phi murium and P. aer u gino sa was
at 700 μ g/m L or higher. A lso , three a ntifungal f lavo-noids were found in heartwood of A. a uriculi formis .
Mihara e t al. [1 8] proposed t hat t he antifunga l activity
of 3, 4’ ,7 , 8- te t ra hy dro xy fla v on e an d te ra ca ci din we re co r-rela ted to the ant iox idant act ivities , where th ese ant ifun-ga l fla v on o id s co ul d sc ave ng e t he fr ee r ad i cal s pr odu ce d
by extracellular fungal en zyme laccase, henc e inhibiting
the mycelia growth of fungus.
The e xtract of C. p u lche r ri ma has b een repo rted to
Inhibit the growth of a broad spectrum of bacteria
[19,37,38]. The extract has also shown antifungal activity
again st p lan t pa thoge ns and ye ast [37,38]. H ow ever,
none of the G ram n egat ive bacteria were i nhib ited b y
C. pulcherrima extracts i n o ur preliminary sc ree nin g.
Mukh erje e an d Ray [39] an d Ali e t a l. [19 ] reported the
presence of all f ive c lasses of phytochemicals in the
leaves while tannins, saponins a nd alka loids w er e
Chew et al . BMC Complementary and Alternative Medicine2011, 11:12
http://www.biomedcentral.com/1472-6882/11/12
Page 7 of 10
detected in the aerial p arts [15]. I n c ont rary, our f ind-ings sho wed al kalo id and s ap onin werenotdetectedin
this plant. The pre sence of gallic acid, ellagic a cid and
fl av o no i d s ( i. e. my r i ce t in , ca t ec hi n, ru ti n, an d q ue r ce ti n)
w er e fo u nd i n C. pul cherrima fl o we r s [ 40 , 4 1] . H o we v er ,
our previo u s report [4] showed t he presence of rutin
but absence of tannins a nd other flavonoids. This can
be explain ed b y t he ec ophy siol ogi cal ef fe ct a nd a biotic
gr owth fact ors that w o u ld po ssib ly be the m ajo r d eter-mining factors w hich could modify the expression of
phyt oche micals in the plant [4] . Ter penoids were found