Structural formula for the amino acidpipecolic acid, which contrary to other amino acids is not used as a building block in proteins. In some plants, pipecolic acid act as a defense compound against microorganisms.[1] Because of its limited presence, pipecolic acid is considered a secondary metabolite.Structural formula for the amino acidproline, that in all living beings is a building block in proteins. Because of its universal presence, proline is considered a primary metabolite.
Secondary metabolites, also called specialised metabolites or secondary products, are a type of natural product (organic compounds produced by living organisms) generated by lifeforms (e.g., bacteria, archaea, fungi, plants, or animals) that are not directly involved in the normal growth, development, or reproduction of the organism. Instead, they generally mediate ecological interactions, which may produce a selective advantage for the organism by increasing its survivability or fecundity. Specific secondary metabolites are often restricted to a narrow set of species within a phylogenetic group. Secondary metabolites often play an important role in plant defense against herbivory and other interspecies defenses. Humans use secondary metabolites as medicines, flavourings, pigments, and recreational drugs.[2]
Secondary metabolites commonly mediate antagonistic interactions, such as competition and predation, as well as mutualistic ones such as pollination and resource mutualisms. Usually, secondary metabolites are confined to a specific lineage or even species,[5] though there is considerable evidence that horizontal transfer across species or genera of entire pathways plays an important role in bacterial (and, likely, fungal) evolution.[6] Research also shows that secondary metabolism can affect different species in varying ways. In the same forest, four separate species of arboreal marsupial folivores reacted differently to a secondary metabolite in eucalypts.[7] This shows that differing types of secondary metabolites can be the split between two herbivore ecological niches.[7] Additionally, certain species evolve to resist secondary metabolites and even use them for their own benefit. For example, monarch butterflies have evolved to be able to eat milkweed (Asclepias) despite the presence of toxic cardiac glycosides.[8] The butterflies are not only resistant to the toxins, but are actually able to benefit by actively sequestering them, which can lead to the deterrence of predators.[8]
Plants are capable of producing and synthesizing diverse groups of organic compounds and are divided into two major groups: primary and secondary metabolites.[9] Secondary metabolites are metabolic intermediates or products which are not essential to growth and life of the producing plants but rather required for interaction of plants with their environment and produced in response to stress. Their antibiotic, antifungal and antiviral properties protect the plant from pathogens. Some secondary metabolites such as phenylpropanoids protect plants from UV damage.[10] The biological effects of plant secondary metabolites on humans have been known since ancient times. The herb Artemisia annua which contains Artemisinin, has been widely used in Chinese traditional medicine more than two thousand years ago.[citation needed] Plant secondary metabolites are classified by their chemical structure and can be divided into four major classes: terpenes, phenylpropanoids (i.e. phenolics), polyketides, and alkaloids.[11]
Structural formula for isopentenyl pyrophosphate (IPP), the carbon atoms of which constitute building blocks in terpenes. Because of the presence of five carbon atoms, the derived building block it is termed a C5 unit.Structural formula for humulene, a monocyclic sesquiterpene (called so because it contains 15 carbon atoms) that is built from three C5 units derived from isopentenyl pyrophosphate (IPP).Skeletal formula of the terpenoid taxol, an anticancer drug.
Terpenes constitute a large class of natural products which are composed of isoprene units. Terpenes are only hydrocarbons and terpenoids are oxygenated hydrocarbons. The general molecular formula of terpenes are multiples of (C5H8)n, where 'n' is number of linked isoprene units. Hence, terpenes are also termed as isoprenoid compounds. Classification is based on the number of isoprene units present in their structure. Some terpenoids (i.e. many sterols) are primary metabolites. Some terpenoids that may have originated as secondary metabolites have subsequently been recruited as plant hormones, such as gibberellins, brassinosteroids, and strigolactones.
Phenolics are a chemical compound characterized by the presence of aromatic ring structure bearing one or more hydroxyl groups. Phenolics are the most abundant secondary metabolites of plants ranging from simple molecules such as phenolic acid to highly polymerized substances such as tannins. Classes of phenolics have been characterized on the basis of their basic skeleton.
Alkaloids are a diverse group of nitrogen-containing basic compounds. They are typically derived from plant sources and contain one or more nitrogen atoms. Chemically they are very heterogeneous. Based on chemical structures, they may be classified into two broad categories:
Structural formula for glucosinolates. The side group R can vary. The structure includes a glucose molecules (to the left), a nitrogen atom derived from an amino acid, and two sulfur atoms, among which one derives from glutathione and the other from sulfate (seen to the left).[13]
Morphine and codeine both belong to the class of alkaloids and are derived from opium poppies. Morphine was discovered in 1804 by a German pharmacist Friedrich Sertürnert. It was the first active alkaloid extracted from the opium poppy. It is mostly known for its strong analgesic effects, however, morphine is also used to treat shortness of breath and treatment of addiction to stronger opiates such as heroin.[16][17] Despite its positive effects on humans, morphine has very strong adverse effects, such as addiction, hormone imbalance or constipation.[17][18] Due to its highly addictive nature morphine is a strictly controlled substance around the world, used only in very severe cases with some countries underusing it compared to the global average due to the social stigma around it.[19]
Opium field in Afghanistan, the largest grower of opium.[20]
Codeine, also an alkaloid derived from the opium poppy, is considered the most widely used drug in the world according to World Health Organization. It was first isolated in 1832 by a French chemist Pierre Jean Robiquet, also known for the discovery of caffeine and a widely used red dye alizarin.[21] Primarily codeine is used to treat mild pain and relief coughing[22] although in some cases it is used to treat diarrhea and some forms of irritable bowel syndrome.[22] Codeine has the strength of 0.1-0.15 compared to morphine ingested orally,[23] hence it is much safer to use. Although codeine can be extracted from the opium poppy, the process is not feasible economically due to the low abundance of pure codeine in the plant. A chemical process of methylation of the much more abundant morphine is the main method of production.[24]
Atropine is an alkaloid first found in Atropa belladonna, a member of the nightshade family. While atropine was first isolated in the 19th century, its medical use dates back to at least the fourth century B.C. where it was used for wounds, gout, and sleeplessness. Currently atropine is administered intravenously to treat bradycardia and as an antidote to organophosphate poisoning. Overdosing of atropine may lead to atropine poisoning which results in side effects such as blurred vision, nausea, lack of sweating, dry mouth and tachycardia.[25]
Resveratrol is a phenolic compound of the flavonoid class. It is highly abundant in grapes, blueberries, raspberries and peanuts. It is commonly taken as a dietary supplement for extending life and reducing the risk of cancer and heart disease, however there is no strong evidence supporting its efficacy.[26][27] Nevertheless, flavonoids are in general thought to have beneficial effects for humans.[citation needed] Certain studies shown that flavonoids have direct antibiotic activity.[28] A number of in vitro and limited in vivo studies shown that flavonoids such as quercetin have synergistic activity with antibiotics and are able to suppress bacterial loads.[29]
The three main classes of fungal secondary metabolites are: polyketides, nonribosomal peptides and terpenes. Although fungal secondary metabolites are not required for growth they play an essential role in survival of fungi in their ecological niche.[31] The most known fungal secondary metabolite is penicillin discovered by Alexander Fleming in 1928. Later in 1945, Fleming, alongside Ernst Chain and Howard Florey, received a Nobel Prize for its discovery which was pivotal in reducing the number of deaths in World War II by over 100,000.[32]
Examples of other fungal secondary metabolites are:
Fungal secondary metabolites can also be dangerous to humans. Claviceps purpurea, a member of the ergot group of fungi typically growing on rye, results in death when ingested. The build-up of poisonous alkaloids found in C. purpurea lead to symptoms such as seizures and spasms, diarrhea, paresthesias, Itching, psychosis or gangrene. Currently, removal of ergot bodies requires putting the rye in brine solution with healthy grains sinking and infected floating.[36]
Bacterial production of secondary metabolites starts in the stationary phase as a consequence of lack of nutrients or in response to environmental stress. Secondary metabolite synthesis in bacteria is not essential for their growth, however, they allow them to better interact with their ecological niche. The main synthetic pathways of secondary metabolite production in bacteria are; b-lactam, oligosaccharide, shikimate, polyketide and non-ribosomal pathways.[37] Many bacterial secondary metabolites are toxic to mammals. When secreted those poisonous compounds are known as exotoxins whereas those found in the prokaryotic cell wall are endotoxins.
Bacteriorubetin, a red-orange carotenoid found in some types of bacteria and archaea.Carotenoids, a pigment produced by different species of bacteria, such as Micrococcus sp.[38][39][40]
Archaea are capable of producing a variety of secondary metabolites, which may have significant biotechnological applications.[41] Despite knowing this, the biosynthetic pathways for secondary metabolites in archaea are less understood than those in bacteria. Notably, archaea often lack some biosynthesis genes commonly present in bacteria, which suggests that they may possess unique metabolic pathways for synthetizing these compounds.[41]
Extracellular polymeric substances can effectively adsorb and degrade hazardous organic chemicals. While these compounds are produced by various organisms, archaea are particularly promising for wastewater treatment due to their high tolerance to saline concentrations and their ability to grow anaerobically.[42]
Selective breeding was used as one of the first biotechnological techniques used to reduce the unwanted secondary metabolites in food, such as naringin causing bitterness in grapefruit.[43] In some cases increasing the content of secondary metabolites in a plant is the desired outcome. Traditionally this was done using in-vitro plant tissue culture techniques which allow for: control of growth conditions, mitigate seasonality of plants or protect them from parasites and harmful-microbes.[citation needed] Synthesis of secondary metabolites can be further enhanced by introducing elicitors into a tissue plant culture, such as jasmonic acid, UV-B or ozone. These compounds induce stress onto a plant leading to increased production of secondary metabolites.
To further increase the yield of SMs new approaches have been developed. A novel approach used by Evolva uses recombinant yeast S. cerevisiae strains to produce secondary metabolites normally found in plants. The first successful chemical compound synthesised with Evolva was vanillin, widely used in the food beverage industry as flavouring. The process involves inserting the desired secondary metabolite gene into an artificial chromosome in the recombinant yeast leading to synthesis of vanillin. Currently Evolva produces a wide array of chemicals such as stevia, resveratrol or nootkatone.
With the development of recombinant technologies the Nagoya Protocol on Access to Genetic Resources and the Fair and Equitable Sharing of Benefits Arising from their Utilization to the Convention on Biological Diversity was signed in 2010. The protocol regulates the conservation and protection of genetic resources to prevent the exploitation of smaller and poorer countries. If genetic, protein or small molecule resources sourced from biodiverse countries become profitable a compensation scheme was put in place for the countries of origin.[44]
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^Zhao ZJ, Pan YZ, Liu QJ, Li XH (June 2013). "Exposure assessment of lovastatin in Pu-erh tea". International Journal of Food Microbiology. 164 (1): 26–31. doi:10.1016/j.ijfoodmicro.2013.03.018. PMID23587710.
^Uys H, Berk M (June 1996). "A controlled double blind study of zuclopenthixol acetate compared with clothiapine in acute psychosis including mania and exacerbation of chronic psychosis". European Neuropsychopharmacology. 6: 60. doi:10.1016/0924-977x(96)87580-8. ISSN0924-977X. S2CID54245612.
^Nisha P, John N, Mamatha C, Thomas M (January 2020). "Characterization of bioactive compound produced by microfouling actinobacteria (Micrococcus Luteus) isolated from the ship hull in Arabian Sea, Cochin. Kerala". Materials Today: Proceedings. International Conference on the Science and Technology of Advanced Materials. 25: 257–264. doi:10.1016/j.matpr.2020.01.362. ISSN2214-7853.
^Yolmeh M, Khomeiri M, Ghorbani M, Ghaemi E, Ramezanpour SS (2017-01-01). "High efficiency pigment production from Micrococcus roseus (PTCC 1411) under ultraviolet irradiation". Biocatalysis and Agricultural Biotechnology. 9: 156–161. doi:10.1016/j.bcab.2016.12.010. ISSN1878-8181.
^Liu BB, Govindan R, Muthuchamy M, Cheng S, Li X, Ye L, et al. (May 2022). "Halophilic archaea and their extracellular polymeric compounds in the treatment of high salt wastewater containing phenol". Chemosphere. 294: 133732. Bibcode:2022Chmsp.29433732L. doi:10.1016/j.chemosphere.2022.133732. PMID35101434.
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