Environmental Factors On Secondary Metabolism of Medicinal Plants

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Acta Scientific Pharmaceutical Sciences (ISSN: 2581-5423)

Volume 3 Issue 8 August 2019


Review Article

Environmental Factors on Secondary Metabolism of Medicinal Plants

Mohi Uddin*
World University of Bangladesh, Bangladesh
*Corresponding Author: Mohi Uddin, World University of Bangladesh, Bangladesh.
Received: April 08, 2019; Published: July 11, 2019
DOI: 10.31080/ASPS.2019.03.0338

Abstract
Plants are unrivaled in the common world in both the number and unpredictability of secondary metabolites they produce, and
the pervasive phenylpropanoids and the heredity explicit glucosinolates speak to two such vast and artificially various gatherings.
Advances in genome-empowered natural chemistry and metabolomic innovations have incredibly expanded the comprehension
of their metabolic systems in assorted plant species. There additionally has been some advancement in explaining the quality ad-
ministrative systems that are critical to their combination, gathering and capacity. Secondary metabolites have essential defense
and flagging jobs, and they add to the general quality of creating and aging natural products. Particularly, light conditions and tem-
perature are exhibited to have an unmistakable job on the organization of phenolic compounds. The present survey centers around
the examinations on components related with the guideline of key secondary metabolites, mostly phenolic compounds, in different
plants. are a helpful cluster of normal items as well as an essential piece of plant defense framework against pathogenic assaults and
environmental stresses. With astounding biological exercises, plant SMs are progressively utilized as drug fixings and nourishment
added substances for remedial, fragrant and culinary purposes. Different hereditary, ontogenic, morphogenetic and environmental
components can impact the biosynthesis and aggregation of SMs. As indicated by the writing reports, for instance, SMs gathering is
unequivocally reliant on an assortment of environmental factors, for example, light, temperature, soil water, soil richness and salti-
ness, and for most plants, an adjustment in an individual factor may modify the substance of SMs regardless of whether different
elements stay steady. Here, we survey with accentuation how every one of single elements to influence the collection of plant sec-
ondary metabolites, and lead a relative examination of applicable normal items in the stressed and unstressed plants. Hopefully, this
narrative survey will diagram a general picture of environmental elements in charge of change in plant SMs, give a handy method to
get reliable quality and high amount of bioactive compounds in vegetation, and present a few proposals for future innovative work.
Keywords: Terms; Medicinal Plants; Organic Compounds; Secondary Metabolite; Biosynthesis

Introduction plants while creating different physiological instruments is through


the generation of an assortment of phytochemicals by which they
While in nourishment plants our fundamental intrigue is the
had the capacity to confront both biotic and abiotic stresses and
starch/sugars, proteins, fats and different nutrients, in restorative
dangers. In this procedure of defense/offense from abiotic stress
plants we search for remedially helpful synthetic substances which
or the attacking illnesses causing life forms or the predators (crea-
are for the most part named as secondary metabolites which are
tures, winged animals, creepy crawlies and herbivorous creatures),
not unreasonably basic for the typical development and improve-
the plant orchestrate an assortment of synthetic compounds. Ob-
ment of the plants/life forms. Plants orchestrate these compounds
viously, plants produce numerous cancer prevention agents for
to ensure themselves for example to change, adjust or guard/insult,
shielding themselves from the oxidative stress. These compounds
from the unfriendly creatures or ailments or the earth. SMs that are
are when all is said in done put away in the leaves or different parts,
valuable in prescription are for the most part polyphenols, alka-
for example, bark, hardwood, natural products, and so forth., with
loids, glycosides, terpenes, flavonoids, coumarins, tannins and so
the goal that the predators or the malady causing creatures can be
forth. The generation of secondary metabolites albeit constrained
either thumped down or incapacitated or even get executed. Much
by qualities however their particular articulation is incredibly af-
of the time, the creation of the secondary metabolites in plant addi-
fected by different components including biotic and abiotic con-
tionally relies upon the relationship of other living creatures, all the
ditions, for example, atmosphere and edaphic factors or other re-
more especially, the plant or soil microorganisms. Such differential
lated living life forms. Over the span of development plants have
articulations of restoratively dynamic standards in plant because of
advanced different physical and substance systems to shield them-
the above said factors seems to have known and surely knew by the
selves from the impulses of nature (dry spell, heat, downpour, flood,
old researchers, when they gave explicit guidelines in the obtain-
and so forth.) and furthermore to guard or insult the predators or
ment of therapeutic plants.
to shield from predators and pathogens. The best adjustment of

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

35

Biosynthesis
The pathways of biosynthesis are in charge of the event of both
essential and secondary metabolites showed in figure 1 biosyn-
thetic reactions are vitality devouring, filled by the vitality dis-
charged by glycolysis of sugars and through the citrus extract cycle.
Oxidation of glucose, unsaturated fats and amino acids results in
ATP development, which is a high-vitality atom shaped by catabo-
lism of essential compounds. ATP is reused in fuel anabolic reac-
tions including middle of the road atoms on the pathways. Though,
catabolism includes oxidation of beginning atoms, biosynthesis
or anabolism includes decrease response. Henceforth, the need of
lessening operator or hydrogen contributor, which is generally the
NADP. These impetuses are known as coenzymes and the most gen-
erally happening is CoA comprised of ADP and pantetheine phos-
Figure 1: Cell Metabolic Cycle and Production of Secondary me-
phate. The most well-known pathways taken for biosynthesis are
tabolites. Plants are sessile organisms and, in order to defend them-
performed through the pentose for glycosides, polysaccharides;
selves against exogenous (a)biotic constraints, they synthesize an
shikimic acid for phenols, tannins, sweet-smelling alkaloids; acetic
array of secondary metabolites which have important physiological
acid derivation malonate for phenols and alkaloids and mevalonic
and ecological effects. Plant secondary metabolites can be classified
acid for terpenes, steroids and alkaloids. As appeared in the figure
into four major classes: terpenoids, phenolic compounds, alkaloids
1, the plan plots how metabolites from the procedure of photo-
and sulphur-containing compounds. These phytochemicals can be
synthesis, glycolysis and Krebs cycle are tapped off from vitality
antimicrobial, act as attractants/repellents, or as deterrents against
producing procedure to give biosynthetic intermediates. By a long
herbivores. The synthesis of such a rich variety of phytochemicals
shot, the essential structure squares utilized in the biosynthesis of
is also observed in undifferentiated plant cells under laboratory
secondary metabolites are gotten from Acetyl-CoA, shikimic acid,
conditions and can be further induced with elicitors or by feeding
mevalonic acid and 1-deoxylulose 5-phosphate [1-7] (Figure 2).
precursors (Source: Guerriero G, Berni R, Muñoz-Sanchez JA, et al.
Production of Plant Secondary Metabolites: Examples, Tips and
Expression of secondary metabolites Suggestions for Biotechnologists. Genes (Basel). 2018;9(6):309.
The nearness of or nonattendance of certain secondary metabo- Published 2018 Jun 20. doi:10.3390/genes9060309).
lites in restorative plants are affected by an assortment of compo-
nents, which incorporate atmosphere/season, edaphic conditions
or the relationship of different plants and other living creatures
number of eggs and the hatchlings that rise up out of these eggs
[8,9]. Another factor that affected the creation of secondary me-
at that point feed on leaves of the plants, some of the time oblit-
tabolites in plants are the entomb connection among plants and
erating the plants through and through by over bolstering. Over
the bug greenery. It is currently commonly acknowledged that the
the span of advancement, the plants started to integrate certain
vegetation and the creepy crawly greenery in a tropical biological
dangerous substance so a decent level of the bolstering hatchlings
system have been co-developing and co-adjusting. A considerable
could be murdered [12-14]. The bug then again started to create
lot of the therapeutic plants are cross-pollinated and they need
obstruction with the goal that a significant number of the hatch-
the assistance of pollinators. In an open territory the breeze could
lings could endure. The plants then again balanced. It orchestrat-
do the capacity, yet in a canopied woods a considerable lot of the
ing an ever increasing number of poisonous compounds. This was
bushes and herbs becoming under the enormous trees can't get
something like the adoration and loathe connection among plants
wind to fertilize. These plants are in this manner intensely relying
and the creepy crawlies, which over the span of a great many long
on the creepy crawlies or even the feathered creatures to fertil-
stretches of advancements have brought about the combination of
ize them. To pull in the creepy crawlies or fowls the plants create
incalculable concoction compounds, for the most part the second-
charming smell (basic oils) and give nectar and dust as sustenance
ary metabolites in plants just as in bugs [15,16]. The changeabil-
to these pollinators. Numerous blooms contain nectar or dust,
ity in living life forms is in reality the protection for survival. The
which are the ordinary nourishment of numerous creepy crawlies
transformative root of cross rearing was for sure a nature's gadget
and feathered creatures [10,11]. The creepy crawlies like honey
for reshuffling of qualities so new variations could be delivered.
bees and butterflies visit many flowers, and take nectar or dust
Thus, the abiotic conditions likewise applied certain impact in the
or both. Amid this procedure they likewise convey dust on their
plants and the plants reacted by creating different synthetic com-
body part, which at that point help in pollinating while at the same
pounds [17]. In outrageous dry spell conditions the desert applies
time visiting different plants. Numerous blooms have basically
a sort of stress on the plants and the plants develop by combining
advanced blossom parts to influence such fertilizations by bugs.
synthetics that would assist them with protecting from stress actu-
These creepy crawlies likewise duplicate on plants. They lay a huge
ated by the desert conditions. An incredible case for this is the plant

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

36

similar sort of fragrance with the comparing synthetic constituents


[18-20].

Importance of secondary metabolites


Secondary metabolites, which are a trademark highlight of
plants, are particularly vital and can secure plants against a wide
assortment of microorganisms (infections, microbes, organisms)
and herbivores (arthropods, vertebrates). Similar to the circum-
stance with all defense frameworks of plants and creatures, a cou-
ple of particular pathogens have developed in plants and have con-
quered the substance defense obstruction. Secondary metabolites,
including anti-infection agents, are delivered in nature and serve
survival capacities for the life forms creating them. Secondary me-
tabolites serve:
• As aggressive weapons utilized against other microbes,
parasites, amoebae, plants, bugs, and substantial creatures;
• As metal transporting specialists;
• As specialists of advantageous interaction among microor-
Figure 2: Biosynthesis scheme of plants secondary metabolites. ganisms and plants, nematodes, bugs, and higher creatures;
Direct examination of secondary metabolite biosynthesis was pos- • As sexual hormones; and
sible with the use of the isotopic tracer technique. This methodol- • As separation effectors.
ogy, applied extensively to primary metabolism beginning in 1935
In spite of the fact that anti-infection agents are not compulsory
and to secondary metabolism from about 1950, was facilitated by
for sporulation, some secondary metabolites (counting anti-micro-
the increasing availability of the 14C isotope. With the use of iso-
bials) invigorate spore arrangement and restrain or animate ger-
topes as tracers, the broad outlines of secondary metabolite bio-
mination. Arrangement of secondary metabolites and spores are
synthesis, reviewed here, were established in the period 1950 to
managed by comparative elements. Consequently, the secondary
1965 (Source: Ronald Bentley. Secondary Metabolite Biosynthesis:
metabolite can:
The First Century. Critical Reviews in Biotechnology Volume 19,
• Slow down germination of spores until a less focused con-
1999 - Issue 1. https://doi.org/10.1080/0738-859991229189)
dition and increasingly positive conditions for development
exist;
• Protect the lethargic or started spore from utilization by
Commiphora wightii; a critical therapeutic plant utilized broadly as
amoebae; or
complimentary drug named 'Guggul'. The restorative piece of the
• Cleanse the quick condition of contending microorganisms
plant is the gum exudates from the stem bark of living plants. This
amid germination [21-24] (figure 3).
gum is customarily gathered from the desert districts of Rajasthan,
Gujarat and even Afghanistan. Incredibly the synthetic information
Environmental stress and secondary metabolites in plants
of this gum uncovered that it doesn't contain the vast majority of
the dynamic compounds. A consistent clarification might be that Environmental factors altogether influence plant development

this plant developing in a warm damp tropical backwoods locale. and biosynthesis of SMs. Plant development and profitability is ad-

It has no desert like conditions and hence there is no doubt of any versely influenced by temperature boundaries, saltiness, and dry

dry season incited stress. A similar plant when developing in des- spell stress. Plant SMs are compounds that have a fundamental im-

ert needs to stand up to dry season prompted stress and the plant pact in the association of plants with abiotic stresses [25]. What's

incorporates the stress beating synthetic substances. There are nu- more, plant development and advancement are additionally to a

merous comparative cases that show that specific explicit climatic great extent intervened by the endogenous dimensions of these

conditions and edaphic circumstances are critical in the creation SMs. A wide scope of SMs are delivered from essential metabolites,

of restoratively attractive therapeutic compounds. Sandalwood is for example, amino acids, lipids, and sugars in higher plants. Spe-

another traditional model. The particular fragrance of sandalwood cific hues, tastes, and scents of plants are related with SMs. Plant

is because of the nearness of certain fundamental oil synthetic con- SMs additionally fill in as fundamental wellsprings of modernly

coctions, generally monoterpenes and sesquiterpenes. The genera- vital synthetic concoctions, flavors, sustenance added substances,

tion of the particular fragrance synthetic compounds is completely and pharmaceuticals [26]. Plants amass such compounds in light

communicated just in those sandalwood trees that develop in cer- of various flagging particles. SM generation is affected by different

tain woods areas of Karnataka. The sandalwood developing in dif- environmental stresses. Environmental elements decide the blend

ferent places in India or somewhere else on the planet don't have a and resulting amassing of SM. Adjustment in any one factor triggers
irritations in the biosynthesis of plant SMs [27].

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

37

Figure 4: Secondary Metabolites and Plant Growth Regulators.


As the plants require oxygen, water, sunlight, and nutrition to grow
Figure 3: Diverse abiotic stresses and the strategic defense
and develop, they do require certain chemical substances to man-
mechanisms adopted by the plants. Outrageous conditions (under-
age their growth and development. These chemicals substances
neath or over the ideal dimensions) limit plant development and
are called Plant Growth Regulators and are produced naturally by
advancement. A horrible situation including outrageous high or
the plants itself. The plant growth regulators are simple organic
low of temperature, saltiness and dry spell represent an intricate
molecules having several chemical compositions. They are also de-
arrangement of stress conditions. Plants can detect and respond to
scribed as phytohormones, plant growth substances, or plant hor-
stresses from multiple points of view that support their sustenance.
mones. Based on their action, plant growth regulators are broadly
They recall past presentation to abiotic stresses and even systems
classified into two major groups: Plant growth promoters and
to defeat them so that reactions to rehashed stresses can be altered
Plant growth inhibitors. (Source: Katerova Z., Todorova D., Sergiev
as needs be. Despite the fact that the outcomes of warmth, dry sea-
I. (2017) Plant Secondary Metabolites and Some Plant Growth Reg-
son, saltiness and chilling are extraordinary, the biochemical reac-
ulators Elicited by UV Irradiation, Light And/Or Shade. In: Ghor-
tions appear to be pretty much comparative. High light force and
banpour M., Varma A. (eds) Medicinal Plants and Environmental
substantial metal lethality additionally produce comparative effect
Challenges. Springer, Cham DOI https://doi.org/10.1007/978-3-
however submergence/flood circumstance prompts degenerative
319-68717-9_6.
reactions in plants where aerenchyma are created to adapt to an-
aerobiosis. It is accordingly, obvious that versatile procedures of
plants against assortment of abiotic stresses are similar to in na-
tae, and spines, yet in addition the generation of different secondary
ture. It might give a vital key to mounting vital resilience to joined
metabolites. Such sorts of plant reactions have been seen against
abiotic stresses in harvest plants (Meena KK, Sorty AM et.al. Abiotic
microscopic organisms, growths, and irritations. These secondary
Stress Responses and Microbe-Mediated Mitigation in Plants: The
metabolites trigger diverse plant defense components as ascorbic
Omics Strategies. Front. Plant Sci., 09 February 2017 | https://doi.
acid, antioxidative chemicals (peroxidase, polyphenol oxidase, li-
org/10.3389/fpls.2017.00172)
poxygenases), salicylic acid, jasmonic acid, and Ca2+ against biotic
stress and furthermore go about as poisons (terpenes, alkaloids,
Differential responses of plants to biotic stress and phenolic compounds) against plant pathogens [30] (Figure 5).

Plants contribute a great deal to this universe yet they need


Engineering of biomass accumulation and secondary metabo-
to confront numerous stresses of biotic or abiotic nature. Biotic
lite production
stress is an extreme environmental imperative to the plant's profit-
ability. Biotic stress incites misfortune in harvest yield presumably Plants are the wellspring of profitable secondary metabolites
more than the total misfortunes from every single other factor. In that are normally utilized in pharmaceutical, nourishment, rural,
any stress, the sort and span are basic for plant development [28]. corrective, and material ventures [31]. Plant cell and tissue culture
Plants utilize different cautious methodologies to endure these innovations can be set up routinely under sterile conditions from
antagonistic elements. Of the different cautious components, one explants, for example, plant leaves, stems, roots, and meristems
is the creation of receptive oxygen species. These cautious com- for both the ways for augmentation and extraction of secondary
ponents against biotic stress are created because of the constant metabolites. In vitro creation of secondary metabolite in plant
cooperation among plant and pathogen [29]. Plants' reactions to cell suspension societies has been accounted for from different
biotic stress are not just the modification in anatomical highlights, restorative plants, and bioreactors are the key advance for their
for example, arrangement of a waxy fingernail skin, trichrome, se- business generation. In view of this lime light, the present audit is

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

38

Figure 6: Plant metabolic engineering strategies to regulate


pharmaceutical terpenoids. Pharmaceutical terpenoids of medici-
Figure 5: Metabolic Engineering of Selected Secondary Me- nal plants are often natural defense metabolites against pathogen
tabolites. The demand for the production of valuable secondary attacks. Elicitors, including biotic and abiotic elicitors, can be used
metabolites is increasing rapidly. While many metabolites can be to activate the pathway of secondary metabolism and enhance the
directly extracted from intact plants, others are routinely produced production of target terpenoids (Xu Lu, Kexuan Tang, Ping Li1. Plant
using cell or organ cultures. The latter, also called Hairy roots when Metabolic Engineering Strategies for the Production of Pharmaceu-
generated through the transformation with the bacterium Agrobac- tical Terpenoids. Front. Plant Sci., 08 November 2016 | https://doi.
terium rhizogenes, are also amenable to molecular modifications. org/10.3389/fpls.2016.01647).
Similar to intact plants metabolic pathways can be altered by in-
troducing homologous or foreign genes. The better the knowledge
of a given pathway, the more efficient will be the genetic alteration. In comparison with a long day of light exposure, a short day of
(Source: Ludwig-Müller J. (2014) Metabolic Engineering of Select- light exposure caused a decrease of, caffeoylquinic acids by about
ed Secondary Metabolites. In: Paek KY., Murthy H., Zhong JJ. (eds) 40% and even an approximately double reduction in the content of
Production of Biomass and Bioactive Compounds Using Bioreactor flavonoid aglycones.
Technology. Springer, Dordrechthttps://doi.org/10.1007/978-94-
017-9223-3_21). Camptothecin (CPT) class of compounds has been exhibited to
be viable against a wide range of tumors. Their atomic target has
been immovably settled to be human DNA topoisomerase I (topo I).
meant to cover phytotherapeutic application and late progression The restorative plant Centella asiatica (L.) Urban contains predom-
for the generation of some imperative plant pharmaceuticals [32]. inantly ursane-type triterpene saponins, the most unmistakable
The expanding business significance of secondary metabolites has one is asiaticoside. It is presently immovably settled that the real
brought about an extraordinary enthusiasm for research concen- bioactivities of C. asiatica leaf separates are because of these sa-
trating on secondary digestion and discovering elective ways for ponins, including memory improvement, wound and vein recuper-
secondary metabolite creation. Plant cell and tissue societies are ating, antihistaminic, antiulcer and antilepsory medications, as an
parts of plant biotechnology and they have been presented as elec- energizer, and as antibacterial, antifungal, and cancer prevention
tive ways for the creation of significant secondary metabolites. agent specialists. As a natural indole alkaloid, the SM camptoth-
Plant innovation gives a constant and dependable hotspot for phar- ecin can react to environmental stresses and its collection rate can
maceutical phytochemicals and can without much of a stretch be change with light illumination conditions. It is realized that eclips-
scaled up [33]. In this manner, plant cell and tissue societies have ing can prompt biochemical changes in plants, especially in leaves,
an extraordinary potential to be utilized as an option in contrast to and overwhelming shading of just 27% full sunlight, for instance,
conventional horticulture for the mechanical creation of secondary can hoist the grouping of camptothecin in leaves of Camptotheca
metabolites [34, 35] (Figure 6). acuminata, though considerably diminish that in the parallel foun-
dations of this tree.
Response to secondary metabolism to light irradiation
The key factors related light radiation include photoperiod (du-
There has been extensive open and logical enthusiasm for the
ration), intensity (quantity), direction and quality (frequency or
utilization of phytochemicals got from dietary parts to battle hu-
wavelength). In response to light radiation, plants are able to adapt
man infections. They are normally happening substances found
to the changes of circumstances by the release and accumulation of
in plants. Ferulic acid (FA) is a phytochemical ordinarily found in
various secondary metabolites including phenolic compounds, tri-
foods grown from the ground, for example, tomatoes, sweet corn
terpenoids and flavonoids, and many of them, have high economic
and rice wheat. It emerges from digestion of phenylalanine and ty-
and utilization value due to the well-known antioxidant property
[36] (Figure 7).

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

39

Metabolite Environment Concentration


Metabolite Class Structural Image Plant Species
Name Factor Change
Phenols Caffeoylquinic Short day of light Decrease X. pensylvanicuim
acids

Phenols Pelargonidin Short day of light Decrease P. contorta

Phenols Catechins Long day of light Increase I. batatas

Phenols Hydroxybenzoic Long day of light Increase I. batatas


acids

Phenols Chlorogenic acid Long day of light Increase V. myrtillus

Table 1: Photoperiod change on the content of various plant SMs [37-41].

Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Alkaloids Camptothecin 27% Full sunlight Increase C. acuminate

Phenols Asiatic acid 70% Shade Increase C. asiatica

Phenols Asiaticoside Full sunlight Increase C. asiatica

Phenols Chlorogenic acid Full sunlight Increase V. myrtillus

Table 2: Light intensity changes on the content of various plant SMs [42-45].

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

40

is a flavonoid found in numerous consumable plants (e.g., tea, broc-


coli, cabbage, kale, beans, endive, leek, tomato, strawberries, and
grapes) and in plants or organic items generally utilized in custom-
ary medication (e.g., Ginkgo biloba, Tilia spp, Equisetum spp, Mor-
inga oleifera, Sophora japonica and propolis). Its enemy of oxidant/
mitigating impacts have been exhibited in different malady models,
including those for encephalomyelitis, diabetes, asthma, and car-
cinogenesis. Additionally, kaempferol go about as a forager of free
radicals and superoxide radicals just as safeguard the movement
of different enemy of oxidant proteins, for example, catalase, glu-
tathione peroxidase, and glutathione-S-transferase. The anticancer
impact of this flavonoid is interceded through various methods of
activity, including against multiplication, apoptosis acceptance, cell-
cycle capture, age of receptive oxygen species (ROS), and hostile to
metastasis/against angiogenesis exercises. Setting Catharanthus
roseus (L.) G. Wear (Apocynaceae) is as yet a standout amongst the
most critical wellsprings of terpene indole alkaloids including an-
ticancer and hypertensive medications as vincristine and vinblas-
tine. These last compounds have complex pathway and numerous
proteins are associated with their biosynthesis. To be sure, ajmali-
cine and catharanthine are critical forerunners their expansion can
prompt upgrade dimensions of particles of intrigue. An immediate
coupling of cantharanthine with vindoline to furnish vinblastine is
nitty gritty alongside key robotic and marking thinks about. With
Figure 7: Interactive effects of UV-B light with other abiotic the culmination of an original absolute blend of vindoline that was
factors on plant growth and production of plant secondary me- reached out to a progression of related analogs. The cancer pre-
tabolites. Under high Photosynthetic active radiation. UV-B light vention agent impacts of the flavonoids rutin and quercetin hinder
increases the net plant photosynthesis in several plant species. oxaliplatin-instigated unending difficult fringe neuropathy.
Higher production of flavonoids can be induced under both UV-B
and high PAR in young and old plant leaves. UV-A radiation has Response of Plant SMs to Temperature
a positive effect on the photosynthesis when plants are exposed
The adjustment of temperature to alkaloids aggregation was ac-
to UV-B. Higher epidermal flavonoids are detected in plants un-
counted for, and high temperature desirable over initiate the bio-
der both UV-A and B radiations in some plant species. Exposition
synthesis of alkaloids. The all-out aggregation of alkaloids (morphi-
of plants to blue light prior or subsequent to UV-B also increases
nane, phthalisoquinoline and benzylisoquinoline) in dry Papaver
the acclimation responses to UV-B by reducing the degradation of
somniferum was confined at low temperature [65]. Conversely, the
photosynthetic pigments. Antagonistic responses between UV-B
all-out dimension of phenolic acids and isoflavonoid (genistein,
radiation and low-Red:far-red ratios have been reported. UV-B
daidzein and genistin) in soybean (Glycine max) roots expanded
can inhibit the shade avoidance associated responses under low-
after the treatment at low temperature for 24 h, and among which
Red:far-red ratios. Likewise, a low-Red:far red ratio can reduce the
the most noteworthy increment of about 310% was seen in genis-
UV-B-mediated induction of plant flavonoids. Increased tempera-
tin after the treatment at 10°C for 24 h, in contrast with the control
ture increases acclimation of plants to UV-B, though it can reduce
[52,53] (Table 4).
the UV-B-mediated induction of plant phenolics. Under combined
UV-B radiation and increased temperature, however, higher emis-
In women, maturing and declining estrogen levels are related
sion of the plant volatile isoprene can be detected in some plant
with a few cutaneous changes, huge numbers of which can be
species. Similarly, under UV-B and water stress conditions, a
turned around or improved by estrogen supplementation. Explor-
positive effect on plant survival is reported. Production of UV-B-
atory and clinical examinations in postmenopausal conditions
induced flavonoids can be modulated by the application of UV-B
demonstrate that estrogen hardship is related with dryness, de-
prior or subsequent to water stress.
cay, fine wrinkling, and poor injury recuperating. The isoflavone
genistein ties to estrogen receptor β and has been accounted for
to improve skin changes. In vitro information has demonstrated
rosine by Shikimate pathway in plants. It displays a wide scope of that the soy isoflavones genistein and daidzein may even animate
helpful impacts against different sicknesses like malignant growth, the expansion of estrogen-receptor alpha positive (ERα+) bosom
diabetes, cardiovascular and neurodegenerative. Kaempferol malignant growth cells at low fixations. 10-Hydroxycamptothecin
(3,5,7-trihydroxy-2-(4-hydroxyphenyl)- 4H-1-benzopyran-4-one)

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

41

Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Phenols Ferulic acid Increase red light Decrease L. sativa

Phenols Kaempferol Increase red light Decrease L. sativa

Alkaloids Catharanthine UV-B Increase C. roseus

Alkaloids Vindoline UV-B Increase C. roseus

Phenols Rutin UV Increase F. esculentum

Phenols Quercetin UV Increase F. esculentum

Phenols Catechins UV Increase F. esculentum

Table 3: Light quality change on the content of various plant SMs [46-51].

(10-HCPT), an indole alkaloid detached from a Chinese tree, Camp- Pelargonidin chloride is an anthocyanidin chloride that has pelar-
totheca sharpen, hinders the movement of topoisomerase I and has gonidin as the cationic partner. It has a job as a phytoestrogen and
a wide range of anticancer action in vitro and in vivo. In any case, its a plant metabolite. It contains a pelargonidin.
utilization has been constrained because of its water-insolubility
and danger with i.v. organization. Isoprene is combined through Reaction of Plant SMs to Soil and Water
the 2-C-methylerythritol-5-phosphate (MEP) pathway that ad- Water stress is a standout amongst the most critical environ-
ditionally delivers abscisic acid (ABA). Increments in foliar free mental stresses that can direct the morphological development and
ABA focus amid dry spell incite stomatal conclusion and may like- advancement of plants, and modify their biochemical properties.
wise adjust ethylene biosynthesis. This first report on α-farnesene Serious water shortage has been considered to decrease the plants
union in Y. lipolytica establishes a framework for future research development, however a few examinations have exhibited that wa-
on creation of sesquitepenes in Y. lipolytica and other nearest yeast ter stress might be conceivable to build the measure of SMs in a
species and will conceivably contribute in its modern generation. wide assortment of plant species [59,60] (Figure 8).

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

42

Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Alkaloids Morphine Low temperature Decrease P. somniferum

Phenols Genistein 10 °C for 24 h Increase G. max

Phenols Daidzein 10 °C for 24 h Increase G. max

Alkaloids 10-hydroxycamp- 40 °C for 2 h Increase C. acuminata


tothecin

Alkaloids Vindoline Short-term heat Increase C. roseus

Alkaloids Catharanthine Long-term heat Increase C. roseus

Terpenes Isoprene High temperature Increase Q. rubra

Terpenes α-farnesene High temperature Increase D. carota

Phenols Pelargonidin Low temperature Increase Z. mays

Table 4: Temperature change on the content of various plant SMs [50,54-58].

Salidroside is segregated from Rhodiola rosea and is one of the gestion, antiarrhythmic impact, and improvement of angiogenesis.
fundamental dynamic segments in Rhodiola species. Rhodiola ro- Tanshinone IIA (Tan-IIA) is gotten from the dried underlying foun-
sea has for quite some time been utilized as a restorative plant and dations of Salvia miltiorrhiza Bunge, a customary Chinese medica-
has been accounted for to have different pharmacological proper- tion. Despite the fact that Salvia miltiorrhiza has been connected
ties, including antifatigue and against stress movement, anticancer, for a long time, the poisonous quality of the mono-constituent of
cancer prevention agent and safe upgrading and animating sexual Salvia miltiorrhiza, tanshinone IIA, is still understudied. Sub-atom-
action, hostile to aggravation, improvement of glucose and lipid di- ic proof found with cryptotanshinone for treatment and avoidance

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

43

Metabolite Class Metabolite Name Structural Image Environment Factor Concentration Change Plant Species
Phenols Salidroside Soil moisture of 55– Increase R. sachalinen-
75% sis

Phenols Tanshinone Severe drought Increase S. miltiorrhiza

Phenols Cryptotanshinone Severe drought Increase S. miltiorrhiza

Alkaloids Codeine Drought Increase P. somniferum

Alkaloids Glycine betaine Drought Increase C. roseus

Phenols Abietic acid Severe drought Increase P. sylvestris

Table 5: Soil water change on the content of various plant SMs [61-64].

of human malignancy. Blend of the perfect solute glycine betaine stances of these metabolites like there is recuperation of the items
presents an extensive level of osmotic stress resilience to Bacillus will be simple and plant societies are especially helpful in the event
subtilis. Ongoing investigation uncovers that abietic acid can be of plants which are troublesome or costly and determination of
created as an injury recuperating specialist. cell lines for high return of secondary metabolites will be simple.
Numerous different precedents could be given plant metabolic de-
Epilogue signing as this exploration zone is growing effectively. Metabolic
building is likely an expansive advance forward yet playing on the
SMs are the helpful regular items that are blended through sec-
qualities won't take care of the considerable number of issues that
ondary digestion in the plants. The generation of some secondary
have kept the improvement of business achievement in the field of
metabolites is connected to the enlistment of morphological sepa-
plant secondary metabolites. Furthermore, Advances in plant cell
ration and it gives the idea that as the phones experience morpho-
societies could give new intends to the savvy, business creation of
logical separation and development amid plant development. It is
even uncommon or colorful plants, their cells, and the synthetic
seen that in-Vitro creation of secondary metabolites is a lot higher
substances that they will deliver. Learning of the biosynthetic path-
from separated tissues when contrasted with non-separated or
ways of wanted compounds in plants just as of societies is regu-
less – separated tissues. There are bunches of favorable circum-

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

44

tion may contain a solitary herb or blends of a few distinct herbs


accepted to have corresponding or potentially synergistic impacts.
Both the crude medications and the completed herbal items made
contain complex blends of natural compounds, for example, unsat-
urated fats, sterols, alkaloids, flavonoids, polyphenols, glycosides,
saponins, tannins, terpenes and so forth. The quality of the com-
pleted item depends on the quality of the crude materials, which is
again relies upon mineral arrangement of soil, topographical region
and so forth. The same number of as 35% of the therapeutic plants
utilized in Indian frameworks of medication are exceedingly cross
pollinated which show the presence of a wide scope of hereditary
changeability in the populaces of these restorative plant species
which thus reflected in the varieties in the piece of secondary me-
tabolites. Environmental and edaphic just as occasional varieties
likewise cause changes in the substance creation of restorative
Figure 8: The effects of drought on soils, plants and their asso- plants. These actualities must be considered while creating qual-
ciated bacterial communities. Drought induces shifts in soil physi- ity parameters principles of therapeutic plants and their completed
cochemistry (upper left), plant phenotype (upper right), root exu- items.
dation (lower right) and soil and rhizosphere microbiome function
(lower left). These shifts are capable of influencing one other; for Bibliography
instance decreases in soil moisture availability (upper left) leads to 1. L Nelson and Michael M. “Lehninger Principles of Biochemis-
a decrease in the rate of plant photosynthesis (upper right), which try 6th Edition David”. Cox Publisher: W.H. Freeman, (2013).
in turn leads to a reduction in the rate of labile carbon exudation
2. Donald Voet., et al. “Fundamentals of Biochemistry: Life at
to the rhizosphere (lower right) and a greater prevalence in bacte-
the Molecular”. Wiley (2016).
ria with oligotrophic life-strategies (lower left), who are less reli-
ant on such simple carbon sources. These shifts lead to a selection 3. William Charles Evans and George Edward Trease. “Trease
for specific phyla (center panel) within the soil, rhizosphere and and Evans Pharmacognosy”. Daphne Evans, Publisher: St.
root microbiome, including enrichment for many Gram-positive, Louis: Elsevier Health Sciences UK (2014).
oligotrophic (middle left) phyla, and concurrent depletion of many
Gram-negative, copiotrophic (middle right) phyla. Members of oth- 4. James E Robbers., et al. “Pharmacognosy and Pharmacobio-
er phyla exhibit a more balanced mixture of enrichment and deple- technology”. Varro E Tyler Publisher: Baltimore: Williams
tion (middle bottom) (Source: Naylor D, Coleman-Derr D. Drought and Wilkins, ©(1996).
Stress and Root-Associated Bacterial Communities. Front. Plant
5. Michael Heinrich., et al. “Fundamentals of Pharmacogno-
Sci., 09 January 2018 | https://doi.org/10.3389/fpls.2017.02223).
sy and Phytotherapy”. Elizabeth M Williamson Publisher:
Churchill Livingstone, (2012).

larly still simple, and procedures are thus expected to create data 6. Aly Farag El Sheikha. “Medicinal Plants: Ethno-Uses to Bio-
dependent on a cell and atomic dimension. In view of the complex technology Era”. Affiliation: Department of Biology, McMas-
and not entirely comprehended nature of plant cells in-vitro soci- ter University, 1280 Main St. West, Hamilton, ON, L8S 4K1,
eties, case-by-contextual analyses have been utilized to clarify the Canada

issues happening in the generation of secondary metabolites from


7. Medicinal Plants: Chemistry and Properties M Daniel Pub-
refined plant cells. Advance research has prevailing with regards
lisher: CRC Press (2016).
to creating a wide scope of profitable secondary phytochemical in
disorderly callus or suspension societies till to date; in different 8. Giweli AA., et al. “The Chemical Composition, Antimicrobial
cases, generation requires increasingly separated small scale plant and Antioxidant Activities of the Essential Oil of Salvia fru-
or organ societies. ticosa Growing Wild in Libya”. Archives of Biological Sciences
65.1 (2013): 321-329.
Conclusion
9. Bruno Leite Sampaio., et al. “Effect of the environment on the
Restorative plants establish primary asset base of practically all
secondary metabolic profile of Tithonia diversifolia: a model
the conventional social insurance frameworks. The majority of the
for environmental metabolomics of plants”. Scientific Reports
herbal medications created as of now in dominant part of the cre- 6 (2016): 29265.
ating nations need appropriate quality determination and bench-
marks. Home grown medications utilized in conventional prescrip-

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

45

10. Claire Brittain., et al. “Pollination and Plant Resources Change 24. Fumihiko Sato. “Plant Secondary Metabolism”.
the Nutritional Quality of Almonds for Human Health”. PLoS
One 9.2 (2014): e90082. 25. Zhang B. “MicroRNA: a new target for improving plant toler-
ance to abiotic stress”. Journal of Experimental Botany 66.7
11. Koppert Biological System Why do pollinators visit flowers?. (2015): 1749-1761.

12. Ferris Jabr Farming a Toxin to Keep Crops Healthy Scientific 26. Singh R., et al. “Microbial metabolites in nutrition, healthcare
American The Sciences (2013). and agriculture”. 3 Biotech. 7.1 (2017): 15.

13. Ryan A Blaedow. “Forest Health Handbook North Carolina 27. Ashraf MA., et al. “Environmental Stress and Secondary
Forest Service 3rd Edition Publisher”. (2011). Metabolites in Plants: An Overview”. Plant Metabolites and
Regulation Under Environmental Stress Chapter 8 (2018):
14. Crop Scouting Manual Field Crop Integrated Pest Manage- 153-167.
ment Program - University of Wisconsin-Extension - Coop-
erative Extension Service (2010). 28. Sulmon C., et al. “Abiotic stressors and stress responses: What
commonalities appear between species across biological or-
15. Douglas J Futuymaa and Anurag A Agrawalb. “Macroevolu- ganization levels?”. Environmental Pollution 202 (2015): 66-
tion and the biological diversity of plants and herbivores”. 77.
Proceedings of the National Academy of Sciences of the United
States of America 106.43 (2009): 18054-18061. 29. Rejeb IB., et al. “Plant Responses to Simultaneous Biotic and
Abiotic Stress: Molecular Mechanisms”. Plants (Basel) 3.4
16. Marcia O Mello and Marcio C. “Silva-Filho Plant-insect in- (2014): 458-475.
teractions: an evolutionary arms race between two distinct
defense mechanisms”. Brazil Journal of Plant Physiology 41.2 30. Saddique M., et al. “Differential Responses of Plants to Biotic
(2002). Stress and the Role of Metabolites”. Plant Metabolites and
Regulation under Environmental Stress (2018): 69-87.
17. “Plant Evolutionary Biology Copyright Publisher Name
Springer, Dordrecht Information Springer Science+ Business 31. Cragg GM and Newman DJ. “Natural products: a continuing
Media B.V. (1988). source of novel drug leads”. Biochimica et Biophysica Acta
1830.6 (2013): 3670-3695.
18. Neeraj Jain and Rajani S Nadgauda. “Commiphora wightii
(Arnott) Bhandari—A Natural Source of Guggulsterone: Fac- 32. Hussain MS., et al. “Current approaches toward production of
ing a High Risk of Extinction in Its Natural Habitat”. American secondary plant metabolites”. Journal of Pharmacy and Bioal-
Journal of Plant Sciences 4.6A (2013): 57-68. lied Sciences 4.1 (2012): 10-20.

19. Nakuleshwar Dut Jasuja., et al. “Review on Bioactive Com- 33. Breitling R., et al. “Metabolomics for secondary metabolite
pounds and Medicinal Uses of Commiphora mukul”. A Review research”. Metabolites 3.4 (2013): 1076-1083.
on Bioactive Compounds and Medicinal Uses of Commiphora
mukul”. Journal of Plant Sciences 7 (2012): 113-137. 34. Eibl R., et al. “Plant cell culture technology in the cosmetics
and food industries: current state and future trends”. Applied
20. Medicinal Plants Utilisation and Conservation 2nd Revised Microbiology and Biotechnology 102.20 (2018): 8661-8675.
and Enlarged Edition Editor Prof. Pravin Chandra Trivedi
Publisher: Aavishkar Publishers, Distributors Jaipur 302 003 35. Wilson SA and Roberts SC. “Recent advances towards de-
(Raj) India. velopment and commercialization of plant cell culture pro-
cesses for the synthesis of biomolecules”. Plant Biotechnology
21. Schäfer H and Wink M. “Medicinally important secondary Journal 10.3 (2012): 249-268.
metabolites in recombinant microorganisms or plants: prog-
ress in alkaloid biosynthesis”. Biotechnology Journal 4.12 36. Yang L., et al. “Response of Plant Secondary Metabolites to
(2009):1684-1703. Environmental Factors”. Molecules 23.4 (2018): 762.

22. Michael Wink “Chapter 11 Importance of plant secondary 37. dos Santos MD., et al. “Effects of caffeoylquinic acid deriva-
metabolites for protection against insects and microbial in- tives and C-flavonoid from Lychnophora ericoides on in vitro
fections”. Advances in Phytomedicine 3 (2007): 251-268. inflammatory mediator production”. Natural Product Com-
munications 5.5 (2010): 733-740.
23. Michael Wink “Plant breeding: importance of plant second-
ary metabolites for protection against pathogens and her- 38. Skrovankova S., et al. “Bioactive Compounds and Antioxidant
bivores”. Theoretical and Applied Genetics 75.2 (1988): 225- Activity in Different Types of Berries”. International Journal of
233. Molecular Sciences 16.10 (2015): 24673-24706.

Citation: Mohi Uddin. “Environmental Factors on Secondary Metabolism of Medicinal Plants”. Acta Scientific Pharmaceutical Sciences 3.8 (2019): 34-46.
Environmental Factors on Secondary Metabolism of Medicinal Plants

46

39. Del Rio D., et al. “Bioavailability of coffee chlorogenic acids 53. Janas KM., et al. “Constitutive elevated accumulation of phen-
and green tea flavan-3-ols”. Nutrient 2.8 (2010): 820-833. ylpropanoids in soybean roots at low temperature”. Plant Sci-
ence 163.2 (2002): 369-373.
40. Monteiro M., et al. “Chlorogenic acid compounds from coffee
are differentially absorbed and metabolized in humans”. The 54. Irrera N., et al. “Dietary Management of Skin Health: The Role
Journal of Nutrition 137.10 (2007): 2196-2201. of Genistein”. Nutrients 9.6 (2017): 622.

41. National Center for Biotechnology Information. PubChem 55. Poschner S., et al. “The Impacts of Genistein and Daidzein on
Compound Database; CID=135, https://pubchem.ncbi.nlm. Estrogen Conjugations in Human Breast Cancer Cells: A Tar-
nih.gov/compound/135 (accessed Jan. 16, 2019). geted Metabolomics Approach”. Frontiers in Pharmacology 8
(2017): 699.
42. Hashimoto T and Yamada Y. “Alkaloid biogenesis: Molecular
aspects”. Annual Review of Plant Biology 45 (1994): 257-285. 56. Ping YH., et al. “Anticancer effects of low-dose 10-hydroxyc-
amptothecin in human colon cancer”. Oncology Reports 15.5
43. Vincent RM., et al. “Sustained harvest of camptothecin from (2006):1273-1279.
the leaves of Camptotheca acuminate”. Journal of Natural
Products 60.6 (1997): 618-619. 57. Yang X., et al. “Heterologous production of α-farnesene in
metabolically engineered strains of Yarrowia lipolytica”. Bio-
44. Gottschalk KW Shade. “leaf growth and crown development resource Technology 216 (2016): 1040-1048.
of quercus rubra, quercus velutina, prunus serotina and acer
rubrum seedlings”. Tree Physiology 14.7-9 (1994): 735-749. 58. National Center for Biotechnology Information. PubChem
Compound Database; CID=67249, https://pubchem.ncbi.
45. Liu Z., et al. “Camptothecin production in Camptotheca acu- nlm.nih.gov/compound/67249 (accessed Jan. 16, 2019).
minata seedlings in response to shading and flooding”. Cana-
dian Journal of Botany 75 (1997): 368-373. 59. Zobayed SMA., et al. “Phytochemical and physiological chang-
es in the leaves of St. John’s wort plants under a water stress
46. Kim OT., et al. “Characterization of the Asiatic Acid Glucos- condition”. Environmental and Experimental Botany 59.2
yltransferase, UGT73AH1, Involved in Asiaticoside Biosyn- (2007): 109-116.
thesis in Centella asiatica (L.) Urban”. International Journal of
Molecular Sciences 18.12 (2017): 2630. 60. Zhu Z., et al. “Impact of fertilization on drought response in
the medicinal herb Bupleurum chinense DC: Growth and
47. Liu LF., et al. “Mechanism of action of camptothecin”. Annals saikosaponin production”. Industrial Crops and Products
of the New York Academy of Sciences 922 (2000): 1-10. 29.2-3 (2009): 629-633.

48. Srinivasan M., et al. “Ferulic Acid: therapeutic potential 61. Zhang BC., et al. “Salidroside decreases atherosclerotic
through its antioxidant property”. Journal of Clinical Bio- plaque formation in low-density lipoprotein receptor-defi-
chemistry and Nutrition 40.2 (2007): 92-100. cient mice”. Evidence-Based Complementary and Alternative
Medicine (2012): 607508.
49. Benyammi R., et al. “Screening and kinetic studies of cath-
aranthine and ajmalicine accumulation and their correlation 62. Wang T., et al. “Evaluation of Tanshinone IIA Developmental
with growth biomass in Catharanthus roseus hairy roots”. Toxicity in Zebrafish Embryos”. Molecules 22.4 (2017). E660.
Pharmaceutical Biology 54.10 (2016): 2033-2043.
63. Chen W., et al. “Molecular evidence of cryptotanshinone for
50. Ishikawa H., et al. “Direct coupling of catharanthine and treatment and prevention of human cancer”. Anti-Cancer
vindoline to provide vinblastine: total synthesis of (+)- and Agents in Medicinal Chemistry 13.7 (2013): 979-987.
ent-(-)-vinblastine”. Journal of the American Chemical Society
130.2 (2008): 420-421. 64. Park JY., et al. “Abietic acid isolated from pine resin (Resina
Pini) enhances angiogenesis in HUVECs and accelerates cuta-
51. Azevedo MI., et al. “The antioxidant effects of the flavonoids neous wound healing in mice”. Journal of Ethnopharmacology
rutin and quercetin inhibit oxaliplatin-induced chronic pain- 203 (2017): 279-287.
ful peripheral neuropathy”. Molecular Pain 9 (2013): 53.

52. Bernáth J and Tétényi P. “The Effect of environmental fac- Volume 3 Issue 8 August 2019
tors on growth. Development and alkaloid production of © All rights are reserved by Mohi Uddin.
Poppy (Papaver somniferum L.): I. Responses to day-length
and light intensity”. Biochemie und Physiologie der Pflanzen
174.5-6 (1979): 468-478.

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