Role of secondary metabolites in plant defense against pathogens

Role of secondary metabolites in plant defense against pathogens

Accepted Manuscript Role of secondary metabolites in plant defense against pathogens Madiha Zaynab, Mahpara Fatima, Safdar Abbas, Yasir Sharif, Muhamm...

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Accepted Manuscript Role of secondary metabolites in plant defense against pathogens Madiha Zaynab, Mahpara Fatima, Safdar Abbas, Yasir Sharif, Muhammad Umair, Muhammad Hammad Zafar, Khalida Bahadar PII:

S0882-4010(18)31278-6

DOI:

10.1016/j.micpath.2018.08.034

Reference:

YMPAT 3119

To appear in:

Microbial Pathogenesis

Received Date: 13 July 2018 Revised Date:

16 August 2018

Accepted Date: 18 August 2018

Please cite this article as: Zaynab M, Fatima M, Abbas S, Sharif Y, Umair M, Zafar MH, Bahadar K, Role of secondary metabolites in plant defense against pathogens, Microbial Pathogenesis (2018), doi: 10.1016/j.micpath.2018.08.034. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

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Role of Secondary Metabolites in Plant Defense against Pathogens.

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Madiha Zaynab1*, Mahpara Fatima2*, Safdar Abbas*3 Yasir Sharif4, Muhammad Umair3,

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Muhammad Hammad Zafar4, Khalida Bahadar

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1. College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, PR.

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China.

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2. College of Crop Science, Fujian Agriculture and Forestry University, Fuzhou 350002, PR

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3. Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University

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Islamabad, Pakistan.

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4. College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou 350002, PR.

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China.

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5. Faculty of Life science University of Agriculture Faisalabad

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6. PARC Institutes of Advanced Studies in Agriculture, NARC, Islamabad, Pakistan

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*Corresponding Author: MADIHA ZAYNAB ,

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[email protected]

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MAHPARA FATIMA [email protected]

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SAFDAR ABBAS [email protected]

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Abstract

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Pathogens get entry into host cell, reproduce there and use biological machinery of host

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plants which is threat to global crop production. Integrated management strategies based

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upon minimizing population and use of resistant cultivars can address this potential problem. In

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developing world farmers are less likely to adopt these approaches instead they prefer the use

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of chemical pesticides. Reckless use of chemical pesticides is destroying our ecosystem. That’s

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why it is required to explore ecofriendly alternatives, like plant based metabolites to control

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pathogens. Studies conducted on different plant-metabolites reported that these metabolite

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can potentially combat plant pathogens. In this study we have also discussed some of plant

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secondary metabolites including alkaloids, flavonoids and phenolics. In this review we tried to

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highlight the new trends in utilizing secondary metabolites for controlling bacterial, viral and

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fungal pathogens with the hope that upcoming drugs will be human and ecosystem friendly.

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Keywords: Plant protection, Natural Product, Phytochemicals, Food security, Immunity.

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Introduction

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Plants have evolved complex defense system to overcome the biotic and abiotic stresses as

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natural systems poses plenty of opposing forces on plants [1]. Variety of stress forces together

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affects the plants so, any change in metabolic physiology of plant cannot be referred to be

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associated with a specific particular stress factor. In context of specific stress, several response

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pathways are invoked, and in signaling response pathways for pathogens and herbivorous

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insects, several inter-connections exists [2-10]. Some of these response pathways are induced by

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infection and some are performed regardless of antimicrobial nature. Formation of pathogen’s

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cell wall degrading enzymes and synthesis of polymeric barriers to hinder pathogen entrance are

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some of the other means of plant defense [11]. Additionally plants have specific recognition and

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signaling systems that enables plant to detect pathogen entrance rapidly and initiate an effective

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defense response [12]. Plants have also evolved to respond subsequent microbes attack in case if

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they get infected.

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Plants synthesize diversity of secondary metabolites which prominently function to protect plants

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against predators and microbes according to toxic nature of microbes and repel the microbes and

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herbivores. Some secondary metabolites help plant to communicate with other organisms and

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some protects plants from abiotic stress e.g. UV-B radiations [13], so these secondary

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metabolites are significantly important for growth and development [14]. Three major types of

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secondary metabolites viz. Phenolics, Terpenes and Nitrogen/Sulfur containing compounds are

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produced in plant’s body. Terpenes have 5-C isoterpenoid as their basic unit that are toxins and

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deters herbivores. Shikimic acid pathway gives the products that forms phenolics which

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imparts defensive ability to plants. Nitrogen and sulfur containing compounds are mainly

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synthesized from amino acids [15, 16]. Defensive role of plant’s secondary metabolites have

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been confirmed by in vitro examining of plants for which expression of secondary metabolites

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was modified by modern techniques [17, 18]. Formation of secondary metabolites is the result of

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millions of years of plant’s interaction with pathogens and it is considered that more than

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100,000 metabolites are known to be involve in plant defense system, so the situation is still not

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clear [19]. Although it is considered that plant with high concentration of secondary metabolites

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is more resistant to biotic and abiotic stresses but their production is thought to be expensive for

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plant growth and reproduction [20, 21]. Function and structure of plant secondary

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metabolites explain that why plants have evolved induced defense, which is characterized

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with increased concentration in stress situations [22]. Several studies have uncovered that

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hundreds of plant compounds possess ecological and chemical defensive role, which have

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opened a new area of research known as ecological biochemistry [23, 24].

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Secondary metabolites in plant interactions with pathogens

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From long time, secondary metabolites have been suggested to interact with pathogenic

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organisms [25, 26] and among longest plant immune response studies one is involvement of

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secondary metabolites in plant interactions with pathogens (Fig.1) [27, 28]. Decades of research

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have demonstrated that a large number of secondary metabolites have proven their role in plant

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defense response to pathogens. Functions of secondary compounds are heavily pooled in

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conserved framework aside from their high structural diversity and several biosynthetic

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pathways are not conserved in plant kingdom [29]. Production and activation of these

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compounds like other conserved mechanisms of plant defense is facilitated by microbial

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detection via defense proteins or MAMPs recognition by pattern recognition patterns [30]. For

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the classification of secondary compounds several criteria has been introduced because of their

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diverse assortment in plant immunity. These criteria include common precursors, core structure

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and mechanism of action. Commonly used classification based on way of synthesis and

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accumulation of defense related phytochemicals. De novo production of metabolites due to an

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infection named as phytoalexins [28, 31] while, Phytoanticipins is a term used for production and

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storage of defense related metabolites in plant tissues [16].

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Secondary metabolites mode of action

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In plants defense system, widely distributed compounds are phenyl propanoids and flavonoids

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which possess different mode of action. Hundreds of antifungal drugs target only 6 processes,

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most of them act parallel to cell signaling compounds and effects physiological activities or act

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on parts of pathogen like; enzyme inhibition, DNA alkylation and reproductive system etc.[32].

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Mostly these compounds have hydroxyl group containing phenolics, which are likely to

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dissociate in phenolate ions. As phenolic hydroxyl groups form ionic bonds and hydrogen bonds

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with peptides and protons so, their higher number results in high astringency and denaturation

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[19]. Without confirmation i.e. proper three-dimensional structure, proteins cannot work

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properly. Protein properties are changed with any change in protein confirmation which can

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prevent crosstalk with other proteins and DNA/RNA. Secondary metabolites interact and

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changes three-dimensional structure of proteins by forming covalent bond with free SH., OH- or

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amino groups, resulting in loss of function or change in protein turnover. Polyphenols form

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hydrogen bonds and stronger ionic bonds. When these weak non-covalent bonds are formed

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concomitantly and act with a protein changes its flexibility resulting in inactivation of protein.

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Polar nature of phenols makes them less toxic compounds because their absorption is less after

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oral intake [19]. An experiment carried out to check the effect of resveratrol and pinosylvin

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(stilbene compounds) on fungi growth using wood decay test with stilbene impregnated aspen

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and birch samples. Plate experiment showed that at pinosylvin concentration which is enough to

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prevent fungal growth, resveratrol enhances the growth [33].

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Secondary metabolites against plant insect

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Secondary metabolites do not reduce the growth and development of plant instead they affect

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the fodder value of plant tissues where they are produce. These are either induced against the

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attack of microbes and insects (phytoalexins) or stored in inactive forms (phytoanticipins) (Fig.2)

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(Table 1). During herbivory, β-glucosidase activated phytoanticipins results in release of biocidal

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aglycones [34]. Hydrolyzation of glucosinolates by myrosinases during tissue disruption is

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classic example of phytoanticipins. Benzoxazinoids (BXs) are another example of

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phytoanticipins that are present among Poaceae. During tissue damage, their hydrolysis by

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plastid targeted β-glucosidase produces biocidal aglycone BXs that acts as insect repellent [35].

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On the other hand phytoalexins includes alkaloids, terpenoids, isoflavonoids, etc., that affects the

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performance of herbivores [36]. Aside from providing defense to plant, secondary metabolites

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improves the fitness of plant. Nuessly 2007 reported that maize HPR to Helecoverpa zea (corn

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eatworm) is due to C-glycosyl flavone maysine and chlorogenic acid. 4,4-dimethyl cyclooctene

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provides defense to sorghum against shoot fly [37].

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Secondary metabolites against plant viruses

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Several secondary compounds of plant metabolism like alkaloids, phenolics, and flavonoids play

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antiviral functions. Due to diversified structures alkaloids have many biologically active

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compounds that effects living organisms [38, 39]. Studies reported some 18000 alkaloids in

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ancient Chinese herbs with antiviral properties. Alkaloid 7-deoxy-trans-dihydronarciclasine

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discovered from plantain lilies (Hosta plantaginea) is anti TMV with least IC50 value i.e. 1.80

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µM [40]. Similarly Bruceine-D present in extract of Brassica javanica possess inhibitory effect

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against PVY, CMV and TMV [41]. It has been studied that application of 100 µgm/L Bruceine-

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D embedded extract of white goosefoot (Chenopodium amaranticolor) inhibited more than 90%

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PVY and CMV infection after 15 minutes [41]. Seventeen quassinoids with IC50 value of 3.42-

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5.66 have been identified as anti TMV infection [42]. Chen et al. [43] evaluated the anti TMV

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properties of Picarma quassioides wood extract and identified a quassinoid with positive results

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and several other β-carboline alkaloids. His further experiments suggested that combined

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application of β-carboline and quassinoids provide infection inhibition of 36.4%-68.4% as

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compared to 25%-47.4% infection inhibition by lonely application of β-carboline @ 50 µgm/l

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[43]. Similarly, An et al. [44] reported the anti TMV activities of 60 and 65% by application of

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Cynanchum

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demethoxytylophorine N-oxide) two alkaloids at 500 µgm/L concentration.

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Plant secondary metabolites as antifungal compounds

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Studies suggest that majority of secondary metabolites possesses antifungal characteristics [45].

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Allied phenolics and flavonoids constitute a large group of phytochemicals [46]. These

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compounds are present in fruit skins and leaves in high concentrations and take part in plant

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defense against pigmentation, UV resistance and disease resistance as shown in (Table 2) [47].

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Phenolics are known to change the cell permeability of microbes and also cause structural and

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functional deformation of membrane proteins which result in distraction of pH gradient, ATP

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production and conservation system, membrane bonded enzymes, substrate utilization for ATP

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production [48, 49].

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Antimicrobial compounds hinders the pathogens growth in apoplast. For example saponins with

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strong antifungal properties α-tomatine (tomato saponin) activates monomeric G-protein

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pathways and phosphotyrosine kinase which binds to cell membrane followed by cell component

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leakage which leads to ROS burst and Ca+2 elevation in Fusarium oxysporum [50]. Different

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saponins resistance against several pathogenic fungi are produced in different plant species [51].

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Large number of linear or cyclic and unsaturated or unsaturated isoprene units constitute the

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terpenes. Some of the best known terpenes are turpentine and camphor (metabolites of

extracts

containing

(7-demethoxytylophorine

and

7-

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odoriferous plants). Some of plant terpenes are industrial and medicinal importance e.g., taxol

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group [52]. Discovery of sesquiterpenoid phytoalexins, zealexins in F. graminearum infected

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maize was result of characterization of physiological responses. Zealexins showed resistance

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against A. flavus, F. graminearum and R. microspores [53]. Antioxidant, antitumor and anti-

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inflammatory properties of flavonoids have reported. Antibacterial activities of secondary

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metabolites have been suggested in one study. Flavonoids have also been reported in liquid

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extracts of legume leaves e.g. Zapoteca portoricensis. These studies suggest anti-pseudomonas

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aeruginosa activity secondary metabolites [54].

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Plant secondary metabolites as antibacterial compounds

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Analysis of Pseudomonas syringae infected Arabidopsis root exudates revealed the defensive

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role of antimicrobial compounds present in root exudates against this bacterium. Out of eight

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strains, seven are unable to cause infection and plants challenged with non-pathogenic strains

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produced more secondary metabolites. Antibacterial activity gained by non-pathogenic bacteria

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was moderate against non-infecting strains. Antibacterial activity of root exudation due to

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infecting strains was nonsignificant [55]. Studies have been carried to clearly demonstrate the

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role of resistive role of phytoanticipins and phytoalexins against pathogens growth. Brassica

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rapa is important world vegetable crop and its quality is affected by the disease caused by

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Xanthomonas campestris pv. campestris (Xcc). Phenolic compounds and glucosinolates can

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confer resistance to Brassica, but little work have done in this context [56].

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Future Prospects

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Plants developed defence system against several biotic and abiotic stresses with the passage

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of time. Aside from the secondary metabolites either induced by infection or demonstrated,

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modern tools are required for correctly assessing the correlation between N and S application and

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resistance management in crops. Number of previous studies have revealed that N and S

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containing secondary metabolites production is affected by amount of these compounds in

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growth medium so, an optimum amount of these nutrients is required for the proper growth of

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plant and resistance against microbes and environmental stresses. Identification of SIR proteins

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induction mechanism might be a great achievement with minimized use of fungicides. For

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efficient organic farming SIR may become a vital tool. That’s why research for development of

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natural pesticides is needed now a days. Gene cassettes for complete metabolic pathways may be

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generated in long term and defense related secondary metabolites may be generated by metabolic

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engineering of plants or in bioreactors. This will help to quickly overcome the plant microbes or

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environmental stresses.

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Tabel 1. List of plant secondary metabolites against Insects. Listed secondary metabolites

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are shown their linked to a specific category and their target insect in specific plan Plants

Categories

Metabolites Terpenoids

Resistance against

Citrus

Terpenoid

Atta cephalotes

Pine

and Monoterpenes

fir Steroids

Common

Tobbaco

bark beetle

[57]

[58]

Phytoecdysones Insect

[59]

Trans-anethole

[60]

fern Terpenoids

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Limonene

Reference

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Secondary

thymol, litura

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and

Spodoptera

citronellal,

Phenolics

Wheat

Willow

Phenolics

Phenolics

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Phenolics

plant

Salix

AC C

Benzoic acid

Strawberry

Benzoic acid

Cotton

padi Galerucella

[62]

lineola Operophtera

[63]

brumata Phenolics

Phenolics Phenolics

Rhopalosiphum [61]

Tetranychus

[64]

urticae Gossypol

Heliothis

[65]

virescens, Heliothis zea Alkaloids

Nightshade Alkaloid

Leptinotarsa

[66]

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potato Benzoxazinoides Gramineae

demissine

decemlineata

DIMBOA

Ostrinia

[67]

nubilalis Cassava

Cyrtomenus

CNglcs

bergi

Glucosides

Cyanogenic

Bitter

Amygdalin and Capnodis

Glucosides

almond

prunasin

tenebronis

Trifolium

Amygdalin and Hypera postica

Glucosides

repens

prunasin

Cyanogenic

Lotus

Cyanogenic

Zygaena

glucosides

filipendulae

CNglcs

Spodoptera

Cyanogenic

P.lunatus

Glucosides

eridania

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Table 2.List Phenolic compound role against Fungus Chemical

Fungus

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Cyanogenic

Glucosides

benzaldehyde

Botrytis cinerea

protocatechuic Colletotrichum acid

Reference [73] [74]

circinans

Salicylic acid

eutypa lata

[75]

Vanillic acid

Phytophthora

[76]

infestans Chlorogenic

Fusarium

acid

oxysporum

[50]

[69]

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plants

[68]

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Cyanogenic

[70]

[71]

[73]

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Naringin

Penicillium

[77]

Aspergillus

[78]

Oleuropein

Phytophthora

[79]

Nobiletin

Phoma

[80]

tracheiphila Genistein

Monilinia

[81]

fructicola Hordatin A

Helminthosporium [82] sativum

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References

213

[1]

M AN U

211

SC

Flavones

RI PT

digitatum

D.J. Ballhorn, S. Kautz, M. Heil, A.D. Hegeman, Cyanogenesis of wild lima bean

214

(Phaseolus lunatusL.) is an efficient direct defence in nature, Plant Signaling and

215

Behavior, 4 (2009) 735-745. [2]

signals in animals and plants, Addison-Wesley, Reading, MA (1996).

217 218

[3]

M.G. Barbour, J.H. Burk, W.D. Pitts, Terrestrialplant ecology, Second edition, Benjamin/Cummings, Menlo Park, Calif 1987.

219 220

W. Agosta,. Bombardier beetle and fever trees: A close up look at chemical warfareand

TE D

216

[4]

R.M. Bostock, R. Karban, J.S. Thaler, P.D. Weyman, D. Gilchrist, Signal interactions in induced resistance to pathogens and insect herbivores, European Journal of Plant

222

Pathology, 107 (2001) 103-111 [5]

R.M. Bostock, Signal conflicts and synergies in induced resistance to multiple attackers,

AC C

223

EP

221

Physiological and Molecular Plant Pathology, 55 (1999) 99-109

224 225

[6]

226

[7]

R. Hell, Molecular physiology of plant sulfur metabolism. Planta, 202 (1997)138-148. B.P.H.J. Thomma, K. Eggermont, I.A.M.A. Penninckx, B. Mauch-Mani, R. Vogelsang, B.P.A. Cammue, W.F. Broekaert, Separate jasmonate-dependent and salicylate-

227 228

dependent defense-response pathways in Arabidopsis are essential for resistance to

229

distinct microbial pathogens. Proc Nat Acad Sci 95 (1998) 15107-15111

230 231

[8]

P. Vijayan, J. Shockey, C.A. Levesque, R.J. Cook, J. Browse, A role for jasmonate in pathogen defense of Arabidopsis. Proc. Nat. Acad. Sci 95 (1998) 7209-7214

ACCEPTED MANUSCRIPT

232

[9]

Science, 171 (1971) 757-770

233 234

R.H. Whittaker, P.P. Feeny, Allelochemicals: chemical interaction between species.

[10]

A. Kusnierczyk, P. Winge, H. Midelfart, W.S. Armbruster, J.T. Rossiter, A.M. Bones, Transcriptional responses of Arabidopsis thaliana ecotypes with different glucosinolate

236

profiles after attack by polyphagous Myzus persicae and oligophagous Brevicoryne

237

brassicae. J Exp Bot. 58 (2007) 2537-2552. [11]

The Plant Cell, 8 (1996) 1773–1791. [12]

27-33.

241 242

A. Schaller, C.A. Ryan, Systemin-a polypeptide signal in plants. Bioessays, 18 (1996)

SC

239 240

K.E. Hammond-Kosack, J.D. Jones, Resistance gene-dependent plant defense responses.

[13]

H. Schafer, M. Wink, Medicinally important secondary metabolites in recombinant

243

microorganisms

244

Journal, 4 (2009) 1684-1703

245

[14]

plants:

progress

in

alkaloid biosynthesis. Biotechnology

G.A. Rosenthal, The biochemical basis for the deleterious effects of L-canavanine. Phytochemistry, 30 (1991) 1055-1058.

246 247

or

M AN U

238

RI PT

235

[15]

G.A. Rosenthal, M.R. Berenbaum, Herbivores: Their interaction with secondary plant metabolites, Vol II Ecological and evolutionary processes, 2ndedition academic press,

249

San Diego (1992).

250

[16]

H.D. Van Etten, J.W. Mansfield, J.A. Bailey, E.E. Farmer, Two classes of plant antibiotics: Phytoalexins versus “phytoanticipins”. Plant Cell 6 (1994) 1191-1192

251

[17]

J.J. Mes, A.A. Van Doorn, J. Wijbrandi, G. Simons, B.J.C. Cornelissen, M.A. Haring.

EP

252

TE D

248

Expression of the Fusarium resistance gene I-2 colocalizes with the site of fungal

254

containment. The Plant Journal, 23 (2000) 183-193.

255

[18]

The

role

of

and phytoanticipins. In: Slusarenko A, Fraser R, Van Loon L, eds.

Mechanisms of resistance to plant diseases, Netherlands: Kluwer Academic Publishers.

257

(2000) 325–370

258

260

J.W. Mansfield, Antimicrobial compounds and resistance. phytoalexins

256

259

AC C

253

[19]

M. Wink, Plant Secondary Metabolism: Diversity, Function and its Evolution. Natural product communications 3 (2008) 1205-1216.

ACCEPTED MANUSCRIPT

261

[20]

E.L. Simms, Costs of plant resistance to herbivory. In plant resistance to herbivores

262

and pathogens.eds. Ecology, evolution and genetics, Fritz RS and Simms EL, Chicago:

263

University of Chicago Press, (1992) 392-425 [21]

Press (1997).

265 266

R. Karban, I.T. Baldwin, Induced responses to herbivory. Chicago: University of Chicago

[22]

C,D, Harvell, R. Tollrian, Why

inducible defenses? In The ecology and evolution of

267

inducible defenses,

268

Princeton University Press (1999) pp: 3–9

273

[25]

[26]

A. Kössel, Über die Chemische Zusammensetzung der Zelle. Archiv für Physiologie (1891) 181–186.

276 277

T. Hartmann, The lost origin of chemical ecology in the late 19th century. Proceedings of the National Academy of Sciences, USA 105 (2008) 4541–4546

274 275

CD, Princeton, New Jersey:

J.B. Harborne, Recent advances in chemical ecology, Natural Products Reports, 6 (1989) 85-109.

272

Harvell

M AN U

[24]

and

J.B. Harborne, Introduction to ecological biochemistry, Third edition. Academic press, New York (1988).

270 271

R

SC

[23]

Tollrian

[27]

K.P. Link,

H.R. Angell, J.C. Walker, The isolation of protocatechuic acid from

TE D

269

eds.

RI PT

264

278

pigmented onion scales and its significance in relation to disease resistance in onions.

279

Journal of Biological Chemistry 81 (1929) 369–375.

280

[28]

K.O. Müller, H. Börger, Experimentelle Untersuchungen über die Phytophthora‐ Resistenz der Kartoffel. Arbeiten aus der Biologischen Reichsanstalt für Land‐ und

282

Forstwirtschaft 23 (1940) 189–231. [29]

Piślewska‐Bednarek, A. Loraine, P. Schulze‐Lefert, A regulon conserved in monocot

284

and dicot plants defines a functional module in antifungal plant immunity. Proceedings of

285

the National Academy of Sciences, USA 107 (2010) 21896–21901.

286 287

[30]

290

I. Ahuja, R. Kissen, A.M. Bones, Phytoalexins in defense against pathogens, Trends in Plant Science 17 (2012) 73–90.

288 289

M. Humphry, P. Bednarek, B. Kemmerling, S. Koh, M. Stein, U. Göbel, K. Stüber, M.

AC C

283

EP

281

[31]

J.D. Paxton, Phytoalexins – a working redefinition. Phytopathologische Zeitschrift 101 (1981) 106–109.

ACCEPTED MANUSCRIPT

291

[32]

the ionome. Chem. Rev. 109 (2009) 4553–4567.

292 293

J. Morrissey, M.L. Guerinot, Iron uptake and transport in plants: the good, the bad, and

[33]

S.K. Seppänen, L. Syrjälä, K. Weissenberg, T.H. Teeri, L. Paajanen, A. Pappinen, Antifungal activity of stilbenes in in vitro bioassays and in transgenic Populus expressing

295

a gene encoding pinosylvin synthase. Plant Cell Reports, 22 (2004) 584–593.

296

[34]

RI PT

294

A.V. Morant, K. Jørgensen, C. Jørgensen, S.M. Paquette, R. Sánchez-Pérez, B.L. Møller,

297

S. Bak, beta-Glucosidases as detonators of plant chemical defense. Phytochemistry. 69

298

(2008)1795-813.

(2000) 195–216.

300 301

L.L. Walling, The Myriad Plant Responses to Herbivores. J. Plant Growth Regul. 19

SC

[35]

[36]

G.S. Nuessly, B.T. Scully, M.G. Hentz, R. Beiriger, M.E. Snook, N.W. Widstrom,

M AN U

299

302

Resistance to Spodoptera frugiperda (Lepidoptera: Noctuidae) and Euxesta stigmatias

303

(Diptera: Ulidiidae) in sweet corn derived from exogenous and endogenous genetic

304

systems. J. Econ. Entomol. 100 (2007) 1887-1895

305

[37]

S.K. Chamarthi, H.C. Sharma, K.L. Sahrawat, L.M. Narasu, M.K. Dhillon, Physico‐ chemical mechanisms of resistance to shoot fly, Atherigona soccata in sorghum,

307

Sorghum bicolor, J. Appl. Entomol. 135(2011) 446-455

308

[38]

TE D

306

M. Moloudizargari, P. Mikaili, S. Aghajanshakeri, H.M. Asghari, J. Shayegh,

309

Pharmacological and therapeutic effects of Peganum harmala and its main alkaloids.

310

Pharmacognosy Reviews, 7 (2013) 199–212. [39]

O. Erharuyia A. Faloduna P. Langer, Medicinal uses, phytochemistry and pharmacology

EP

311

of Picralima nitida (Apocynaceae) in tropical diseases: A review, Asian Pacific Journal of

313

Tropical Medicine 7 (2014) 1-8.

314

[40]

Y.H. Wang, Z.K. Zhang, F.M. Yang, Q.Y. Sun, H.P. He, Y.T. Di, S.Z. Mu, Y. Lu, Y. Chang, Q.T. Zheng, M. Ding, J.H. Dong, X.J. Hao, Benzylphenethylamine Alkaloids

315

from Hosta plantaginea with Inhibitory Activity against Tobacco Mosaic Virus and

316

Acetylcholinesterase J. Nat. Prod., 70 (2007) 1458–1461

317 318

AC C

312

[41]

E. Shen, J. Zou, F.H. Behrens, L. Chen, C. Ye, S. Dai, L. Fan, Identification, evolution,

319

and expression partitioning of miRNAs in allopolyploid Brassica napus . Journal of

320

Experimental Botany, 66 (2015), 7241–7253.

ACCEPTED MANUSCRIPT

321

[42]

X. Yan, J. Chen, Y.T. Di, X. F, J.H. Dong, P. Sang, Y.H. Wang, H.P. He, Z.K. Zhang,

322

X.J. Hao, Anti-Tobacco Mosaic Virus (TMV) Quassinoids from Brucea javanica (L.)

323

Merr. . Agric. Food Chem., 58 (2010) 1572–1577 [43]

inhibition of the glycine receptor, Journal of Neurochemistry 110 (2009) 1685-1694

325 326

X. Chen, A. Brett, C. Joseph, W. Lynch, Molecular determinants of β‐carboline

[44]

RI PT

324

T. An, R.Q. Huang, Z. Yang, D.K. Zhang, G.R. Li, Y.C. Yao, J. Gao, Alkaloids from

327

Cynanchum komarovii with inhibitory activity against the tobacco mosaic virus.

328

Phytochemistry. 58 (2001) 1267-1269. [45]

J. Koga, M. Shimura, K. Oshima, N. Ogawa, T. Yamauchi, N. Ogasawara,.

SC

329

Phytocassanes A, B, C and D, novel diterpene phytoalexins fromrice,Oryza sativa L.

331

Tetrahedron 51 (1995) 7907–7918.

332

[46]

M AN U

330

A. Crozier, I.B. Jaganath, M.N. Clifford, Phenols, poliphenols andtannins: an overview,

333

inPlant Secondary Metabolites: Occurrence, Structureand Role in the Human Diet, eds A.

334

Crozier, M. N. Clifford, and H. Ashihara(Oxford, UK: Blackwell Publishing Ltd) (2008)

335

1–24. [47]

mankind already?Biochemistry (Lond) 22 (2000) 37–40.

337 338

W.S. Pierpoint, (2000). Why should plants make medicine – don’t theydo enoughfor

[48]

TE D

336

T.L.C. De Oliveira, R. de Araújo Soares, E.M. Ramos, M. das Graças Cardoso, E. Alves, R.H. Piccoli, Antimicrobial activity ofSatureja montana L. essential oil against

340

Clostridium perfringens type A inoculated in mortadella-type sausages formulated with

341

different levels of sodium nitrite.Int. J. FoodMicrobiol.144 (2011) 546–555. [49]

fresh strawberries. Food Control 28 (2012) 157–162.

343 344

M.M El-Mogy, B.W. Alsanius, Cassia oil for controlling plantand human pathogens on

[50]

AC C

342

EP

339

S.I Ito, T. Ihara, H. Tamura, S. Tanaka, T. Ikeda, H. Kajihara, alpha-Tomatine, the major saponin in tomato, induces programmed cell death mediated by reactive oxygen species

345

in the fungal pathogen Fusarium oxysporum. FEBS Lett.581 (2007) 3217–3222

346 347

[51]

A. Osbourn, Saponins and plant defence—a soap story. Trends Plant Sci.1 (1996) 4–9.

348

[52]

J. Bohlmann, C.L. Keeling, Terpenoid biomaterials. Plant J.54 (2008) 656–669.

349

[53]

A. Huffaker, F. Kaplan, M.M. Vaughan, N.J. Dafoe, X. Ni, J.R. Rocca, Novel acidic

350

sesquiterpenoids constitute a dominant class ofpathogen-induced phytoalexins in maize.

351

Plant Physiol.156 (2011) 2082–2097.

ACCEPTED MANUSCRIPT

352

[54]

K.N. Agbafor, E.I. Akubugwo, M.E. Ogbashi, P.M. Ajah, C.C. Ukwandu, Chemical and

353

antimicrobial properties of leaf extracts of Zapoteca portoricensis, J. Med. Plant. 5 (2011)

354

605-612.

355

[55]

H.P. Bais, T.S. Walker, F.R. Stermitz, R.A. Hufbauer, J.M. Vivanco, Enantiomericdependent phytotoxic and antimicrobial activity of (+/-)-catechin. A rhizosecreted

357

racemic mixture from spotted knapweed, Plant Physiol. 128 (2002)1173-1179.

358

[56]

RI PT

356

P. Velasco, M. Lema, M. Francisco, P. Soengas, M.E. Cartea, In vivo and in vitro effects of secondary metabolites against Xanthomonas campestris pv. campestris. Molecules. 18

360

(2013) 11131-11143. [57]

phytochemical ecology.London: Academic Press (1972) 13-24

362 363

[58]

S.C. Trapp, R.B. Croteau, Genomic organization of plant terpene synthases and molecular evolutionary implications. Genetics. 158 (2001) 811-832

364 365

J.M. Cherrett, Chemicai aspects of plant attack hy ieaf-cutting ants. In: Harborne JB, ed.

M AN U

361

SC

359

[59]

D. Canals, J. Irurre-Santilari, J. Casas, The first cytochrome P450 in ferns. Evidence for

366

its involvement in phytoecdysteroid biosynthesis in Polypodium vulgare. FEBS J. 272

367

(2005) 4817-4825. [60]

L.A. Hummelbrunner, M.B. Isman, Acute, sublethal, antifeedant, and synergistic effects

TE D

368 369

of monoterpenoid essential oil compounds on the tobacco cutworm, Spodoptera litura

370

(Lep., Noctuidae). J Agric Food Chem. 49 (2001) 715-720.

371

[61]

B. Leszczyński, Changes in phenols content and metabolism in leaves of susceptible and resistant winter wheat cultivars infested by Rhopalosiphum padi (L.) (Hom., Aphididae).

373

1985. [62]

Leaf Phenolic Chemistry in Salix dasyclados and Susceptibility to Galerucella lineola

375

(Coleoptera), Oikos 47 (1986) 205-210.

376 377

[63]

T. Ruuhola, O.P. Tikkanen, J. Tahvanainen, Differences in host use efficiency of larvae of a generalist moth, Operophtera brumata on three chemically divergent Salix species. J

378

Chem Ecol. 27 (2001) 1595-615.

379 380

S. Larsson, A. Wirén, L. Lundgren, T. Ericsson, Effects of Light and Nutrient Stress on

AC C

374

EP

372

[64]

A. Luczynski, M.B. Isman, D.A. Raworth, Strawberry Foliar Phenolics and Their

381

Relationship to Development of the Twospotted Spider Mite. J Econ Entomol. 83 (1990)

382

557–563.

ACCEPTED MANUSCRIPT

383

[65]

F.G. Maxwell, J.N. Jenkins, W.L. Parrott, Influence of Constituents of the Cotton Plant

384

on Feeding, Oviposition, and Development of the Boll Weevil. J Econ Entomol. 60

385

(1967) 1294–1297. [66]

New York (1988).

387 388

[67]

H.M.

Niemeyer,

Hydroxamic acids

(4-hydroxy-1,4-benzoxazin-3-ones), defence

chemicals in the gramineae. Phytochemistry. 27 (1988) 3349-3358

389 390

J.B. Harborne, Introduction to ecological biochemistry, Third edition. Academic press,

RI PT

386

[68]

R. Croteau, T. Kutchan, N. Lewis, Chapter 24: Natural products (secondary metabolites). In: Buchanan, B., Gruissem, W., Joneas, R. (eds), Biochemistry and Molecular Biology

392

of Plants, American Society of Plant Biologists, Rockville, MD, (2000) 1250 -1268. [69]

J. Malagon, A. Garrido, Relation between cyanogenic glycosides content and the

M AN U

393

SC

391

394

resistance to Capnodis tenebrionis (L.) in stone fruits. Boletin de Sanidad Vegetal 16

395

(1990) 499-503.

396

[70]

M.M. Ellsbury, G.A. Pederson, T.E. Fairbrother, Resistance to foliar feeding hipergine

397

weerils (Coleoptera, Curculionidae) in cyanogenic white clover. J Econ Entomol. 85

398

(1992) 2467-2472 [71]

M. Zagrobelny, S. Bak, C.E. Olsen, B.L. Møller, Intimate roles for cyanogenic glucosides

TE D

399 400

in the life cycle of Zygaena filipendulae (Lepidoptera, Zygaenidae). Insect Biochem Mol

401

Biol. 37 (2007) 1189-1197.

402

[72]

L.B. Brattsten, Cytochrome P-450 involvement in the interactions between plant terpenes and insect herbivores, pp. 173-195. In P. A. Hedin [ed.], Plant resistance to insects. ACS

404

(Am. Chem. Soc.), Washington, DC (1983). [73]

greenhouse isolates of Botrytis cinerea. Plant. Dis. 83 [1999] 569-575.

406 407

[74]

J.C. Walker, M.A. Stahman, Chemical nature of disease resistance in plants. Anna. Rev. plant Physiol. 6 (1955) 351-366

408 409

L.F. Yourman, S.N. Jeffers, Resistance to benzimidazole and dicarboximide fungicides in

AC C

405

EP

403

[75]

V. Lattanzio, D. De Cicco, D. Di Venere, G. Lima, M. Salerno, Antifungal activity of

410

phenolics against fungi commonly encountered during storage. Ital. J. Food Sci. 6 (1994)

411

23-30.

412 413

[76]

J.B. Harborne, Recent advances in chemical ecology, Natural Products Reports, 6 (1989) 85-109.

ACCEPTED MANUSCRIPT

414

[77]

M.C. Arcas, J.M. Botía, A.M. Ortuño, J.A. Del Río, UV irradiation Alters the Levels of

415

Flavonoids Involved in the Defence Mechanism of Citrus aurantium Fruits against

416

Penicillium digitatum, European Journal of Plant Pathology (2000), 06,617–622

417

[78]

M. Weidenbörner, H. Hindorf, H.C. Weltzien, Aneffective treatment of legume seeds with flavonoids and isoflavonoids against storage fungi of the genus Aspergillus. Seed

419

Sci Technol 20 (1992) 447-463

420

[79]

RI PT

418

J.A. Del Río, M.C. Arcas, O. Benavente-García, F. Sabater, A. Ortuño Changes of polymethoxylated flavones levels during development of Citrus aurantium (cv. Sevillano)

422

fruits. Planta medica 64 (2003) 575-576 [80]

Sumere, eds. Biochemistry of Plant Phenolics. Rec. Adv. Phytochem. 12 (1979) 557-588.

424 425

[81]

P.N. Johnson Effects of soil phosphate level and shade on plant growth and mycorrhizas, New Zealand Journal of Botany (New Zealand), 1976 14(4):333-340

426 427

J. Friend, Phenolic substances and plant disease. In T. Swain, J. Harborne and C. F. Van

M AN U

423

SC

421

[82]

J.C. Overeem, Pre-existing antimicrobial substances in plants and their role in disease

428

resistance. In 'Biochemical Aspects of Plant-Parasite Relationships' (J. Friend and D. R.

429

Threlfall, eds), (1976)195-206. Academic Press, London.

EP AC C

431

TE D

430

M AN U

SC

RI PT

ACCEPTED MANUSCRIPT

432

TE D

435

mechanism of species against microbial fungi and virus.

EP

434

Fig1.Schematic classification of Secondary metabolites that may be involved in defence

AC C

433

EP

437

Fig 2: Profiling Plant secondary metabolites and their role in plant defense system

AC C

436

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1.Plants synthesize diversity of secondary metabolites which prominently functions to protect plant.

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2.Secondary metabolites induced against the attack of microbes and insects 3.We have highlight the new trends in utilizing secondary metabolites for controlling bacterial,

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viral and fungal pathogens and insects.