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secondary plant substance

A class of organic compounds produced by plant secondary metabolism with a wide variety and generally less content
synonym Secondary metabolites (Secondary metabolites) generally refer to secondary plant substances
Botany secondary metabolism A class of organic compounds with a wide variety and generally less content, also known as Secondary metabolites It is mainly divided into nitrogen containing organic matter Terpenoid and Phenolic compounds Three categories, such as pigment , alkaloids Terpenoids , antibiotics, etc. They are different from the primary metabolites in terms of distribution and function in addition to their different ways of production. The distribution of secondary substances is limited, only appearing in certain species, organs, tissues or cells. In terms of function, some secondary substances such as plant hormones, as regulators of growth and development, have become important substances of life; Some actions Attractant Repellent Antifeedant And antimicrobials are of great ecological significance.
Chinese name
secondary plant substance
Foreign name
secondary plant substance
Alias
Secondary metabolites
English
secondary plant substance
Composition
Nitrogen containing organics, terpenoids, phenols, etc
Features
More varieties, less content

brief introduction

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except Sugar Fat nucleic acid and protein Equibasic organic compound outside, Plant body There are many other organic substances in the Terpenoids Phenols and alkaloid They are composed of sugars, fats, amino acids and other organic substances metabolize The derived substance is therefore called secondary plant substance [1] The so-called secondary plant substances refer to a variety of organic substances that exist in plants and have no direct relationship with the growth and development of plants, but play an important role in plant adaptation to adverse environments or resistance to pathogens, as well as plant metabolic regulation, also known as secondary products or natural compounds. Secondary plant substances are different from primary metabolites such as amino acids, nucleotides, sugars and membrane lipids photosynthesis Respiration , assimilate transport, growth and differentiation and other physiological processes, there is no direct or obvious role. In addition, the production and distribution of secondary plant substances are often limited to one or several plant species that are similar in taxonomy primary metabolite It exists in all plants. Secondary plant substances stored in vacuoles or cell walls are the final products of metabolism. Except for a few, most of them no longer participate in metabolic activities.

Role of secondary plant substances

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Organic compounds produced in plants but not essential in their growth, development, reproduction and other life activities; Mainly divided into Nitrogenous organic matter Terpenoid and Phenolic compounds Three categories, including non Protein amino acid amine , alkaloids Phenols , benzene propane Acids Coumarins Flavonoids Cyanogenic glycoside lipid Terpenoids anthraquinone And glucosinolates. Its production and distribution are limited, that is, certain secondary substances only appear in specific species, organs, tissues or cells, as well as in specific growth and development periods, and the amount produced is strongly affected by environmental conditions. It plays an important role in the survival and development of plants. [1]
Some are used as growth regulators, such as plant hormones and Growth inhibitor Some actions Attractant Repellent Antifeedant And antimicrobials are of great ecological significance. Some secondary substances have great application value in industry and medicine, such as rubber, ginsenoside, etc. Plant secondary substances There are many varieties with different chemical structures, but they all originate from a few precursors, such as acetic acid Shikimic acid and Isopentene pyrophosphate Etc. These precursors are often found in primary metabolism The critical branch point position in. [1]

Factors affecting the formation of secondary plant substances

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The formation of plant secondary substances is not only related to the growth and development of plants, but also strongly affected by environmental conditions such as light, temperature, rainfall and nutrients. Therefore, in different latitudes, altitudes, climates and soil conditions, the content of secondary substances in plants varies greatly. For example, the content of alkaloid quinine in the bark of Cinchona is up to 15%, while in rainy season soil moisture High hour cinchona It does not produce quinine. In alpine plants Flavonoids The content of substances is much higher than that of the same kind of plants on the flat land. Proper application of nitrogen fertilizer can improve lupin and barley Alkaloid content in. Ammoniacal nitrogen relatively Nitrate nitrogen It is more conducive to the formation of alkaloids in Ligusticum ligusticum. In recent years, there have been many successful cases of using plant tissue culture technology to produce secondary biomass. Through the regulation of the culture environment, some have increased the content of secondary biomass, and some have changed the type of secondary biomass. in China, Ginseng three seven Lithospermum , Coptis chinensis and other medicinal plants cell culture All have achieved success. Such as Lithospermum cell suspension culture Generated Naphthoquinones The content of pigment is 8 times higher than that of the original plant. [1]

Significance of secondary plant substances

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On the surface, plants can not move and will not take the initiative to fight back. They have a long life cycle and are at a disadvantage in the relationship with insects. However, insects are small in size, short in life cycle and high in reproduction rate. They can quickly adapt to the changing environment. Moreover, insects have wings and can migrate from far places and find food resources. However, plants are still lush, covering most of the land surface. Obviously, plants have effective physical, chemical and developmental resistance mechanisms. The mechanism of chemical resistance mainly depends on plant secondary substances: understanding plant secondary substances is a key to study the relationship between insects and plants.
Although Julus Von Liebig pointed out in 1858 Plant secondary substances stay Plant resistance However, some botanists insist that plant secondary substances are only wastes of plant metabolism; It was not until the second half of the 20th century that people unified their understanding and gradually realized the significance of plant secondary substances (Mothes 1995). Fraenkel (1959) further emphasized the role of plant secondary substances in defense against insects and other natural enemies. The secondary substances of plants are more important and effective than any other single natural factors in resisting the invasion of diseases and pests. Not only that, plant secondary substances also play an important role in resisting adverse physical and chemical environment.
It is generally believed that the chemical composition of different parts of plants and between plants are similar (i.e. homogeneous). In fact, the chemical composition of plants is different in space and time, that is, heterogeneous. This heterogeneity in chemical composition and structure of the plant world has formed a huge resistance barrier against insect damage. Here, resistance refers to the characteristics of plants that can avoid or reduce the damage of plant eaters. Resistance and defense are not synonyms, because "defense" means the purpose of evolution, while "resistance" is more neutral, so most people tend to use the word "resistance". [2]

Nitrogenous compound

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Including alkaloids, non Protein amino acid , Amines and Cyanogenic glycoside Etc. [1]

alkaloid

A class of nitrogen-containing alkalinity natural product More than 5500 alkaloids are found in about 4000 plants, mainly distributed in Dicotyledon Medium. Alkaloids are divided into three categories: true alkaloids contain nitrogen Heterocycle Nuclear, e.g Isoquinoline alkaloid Class; The original alkaloids do not have heterocycles and are usually simple amines, such as cactus alkaloids and ephedrine. Both true alkaloids and protoalkaloids are derivatives of amino acids, and some protoalkaloids may be precursors of true alkaloids; Pseudoalkaloids are not derivatives of amino acids, but are derived from Terpenoids purine and Sterols Material production, Pseudoalkaloid include Theobromine And caffeine, both Methylation Purine. Most alkaloids are bitter and toxic, and have strong and specific effects on human nerve centers. as morphine atropine berberine vincristine quinine and Hyoscyamine And so on are important drugs. Some alkaloids can protect plants from animals. The phenomenon that insects choose to invade one or a few plants may be related to the effect of alkaloids. [1]

Non protein amino acids

About 400 species have been identified, which are rich in some legume seeds, most of which are toxic. Because their structures are similar to protein amino acids, they can be wrongly mixed into proteins to form toxic proteins, which affect the normal metabolism of organisms and cause death Antimetabolite as Lily of the valley Ammonia can interfere proline Synthesis or utilization of. wrong Protein amino acid It can protect plants themselves. as Oil hemp vine Plant seeds contain Tyrosine Structurally similar L-dopa It is toxic to insects and can protect seeds from insects. But this substance is non-toxic to mammals and can be used as a treatment Parkinson's disease Drugs. [1]

amine

About 100 kinds of amine secondary substances have been identified. stay seed plant It is widely distributed in the middle part of the plant and often exists in flowers. It has a foul smell and can repel animals and attract some insects pollination Some amines have hallucinogenic effects. [1]

Cyanogenic glycoside

Class I is composed of Decarboxylic amino acid Formed O- Glycoside Cyano group come from Alpha carbon atom And amino groups. Cyanogenic glycoside By beta glucosidase (e.g Bitter almond enzyme )And ocn hydrolase hydrolysis Can be generated later Hydrocyanic acid There are about 30 kinds of cyanogenic glycosides with identified structures, such as flax Picrin Cherokerin , amygdalin Hundred Vein Root Glycosides and Maize Cyanoside Etc. Amygdalin exists in apricot, peach, plum and apple seeds and is generated after enzymatic hydrolysis of bitter almond glucose Benzaldehyde And hydrocyanic acid. stay cherry tree and peach Leaves and Sudan grass And others Sorghum Cyanogen glycosides also exist in plants, and people and animals will die of poisoning due to the production of hydrocyanic acid after eating them by mistake. [1]

terpenoids and steroids

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seed plant It can form various terpenoids and Steroid About 3500 structures have been identified. They are composed of isopentene unit, which is formed by acetic acid - Mevalonate Pathway biosynthesis. By two Isopentene (C5) Unit synthesis Monoterpene , such as myrcene Limonene menthol camphor And so on volatile oil Composition; Synthesis from three isopentene units Sesquiterpene , such as plant hormone abscisic acid , Intestinal Parasitics Yamato Year Etc., found in recent years Compositae Contains multiple sesquiterpenes lactone , has anti-cancer and sensitization effects; Diterpenoids are composed of four isopentene units, such as plant hormones gibberellin anticatarrhals Andrographolide Etc; Synthesized from 5 isopentene units Bisquiterpene There are few in nature, such as amperocoelin from fungi and spongin isolated from sponges; Consists of 6 isopentene units Triterpene Ginseng The main components of Triterpene saponin , some Cardiac glycoside This is also true; 8 Isopentene The unit forms terpene, such as Carotene ; It is composed of multiple isopentene units, such as rubber. Steroids They are not true triterpenes, but have C27-C29 skeletons rather than C30 skeletons. Because their biosynthetic precursors are all C30 Spinalene , so it is often considered together with triterpenes. Steroidal cholesterol And its esters are important components of biofilm. Cholesterol is also the raw material for biosynthesis of steroid hormones, which is synthesized in many plants Ecdysone Of Steroid hormone Ecdysone can affect insect metamorphosis, and can be used to control the development and behavior of silkworm in agriculture Pollution-free pesticide Pest control. [1]

Phenolic compounds

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Include simple Phenols flavonoid And quinones. [1]

Simple phenols

Contains a quilt hydroxyl Substituted benzene ring Compounds. It is widely distributed in plant leaves and other tissues. They have the effect of regulating plant growth, such as 4- Hydroxybenzene Acid salicylic acid P-coumaric acid Gallic acid coumarin And 7-hydroxy-6-methoxycoumarin; At high concentrations Plant growth inhibitor Its inhibition mechanism is mainly through interference with plants growth hormone (In particular Indole acetic acid )Role of. They are also related to the disease resistance of plants, chlorogenic acid and Coumarinoid They have been proved to be important disease resistant substances in plants. Antibiotics produced when plants are attacked by pathogens phytoalexins It also contains many phenols. higher plant Interspecific Mutual restriction phenomenon , also with Phenols The secretion of substances. There are two main pathways for the biosynthesis of simple phenols, namely Shikimic acid pathway and acetic acid - Malonic acid The former is mainly green plants, Heterotrophic microorganism The latter is dominant. [1]

Flavonoids

A large category of benzene Chromone Plant based on environmental system natural product Press Pyran ring The oxidation degree of can be divided into Anthocyanin flavone isoflavone and Flavanone Four categories. Flavonoids It is water-soluble, and is usually associated with Pentose or Hexose (sometimes with disaccharides or Trisaccharide )Cheng Glycoside Form exists. Flavonoids There are many kinds. The yellow, orange, red, blue and other pigments of plant flowers, leaves, fruits and other parts are mainly Flavonoids Some flavonoids are associated with auxin ( Indole acetic acid )Control of activity, e.g Quercus bark Ketogenic inhibition Indoleacetic acid oxidase Active, while 4, 5, 7- Trihydroxyflavone Alcohols can promote the activity of this enzyme. Some isoflavones are phytoalexins , such as the tincture to avoid killing accumulated after pea tissue is infected by bacteria. Some isoflavones have similar estrogen Activity. Some flavonoid It is highly toxic to some animals, such as rotenone Most flavonoids and isoflavones are non-toxic to mammals, and some can be used for medicine, such as Vitamin P and rutin Some Flavonoids It is unique to some plant groups and can be used as a basis for plant classification. [1]

Quinones

By benzene or more cyclic hydrocarbon Aromatic dioxides derived from hydrocarbons (such as naphthalene, anthracene, etc.). According to its ring system, it can be divided into Benzoquinone Naphthoquinone and Anthrone Etc. Quinones are widely found in biological group Medium. With long Isoprenoid Side chain quinones, such as Plastoquinone Ubiquinone And quinones participate in basic life activities such as photosynthesis and respiration. Quinones are yellow, orange or red, which is also the reason why plants are colored. [1]