Bioactive Secondary Metabolites of Microbial Symbionts

A special issue of Microbiology Research (ISSN 2036-7481).

Deadline for manuscript submissions: 30 June 2024 | Viewed by 1942

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Centre for Applied Research, Innovation and Entrepreneurship, Lethbridge College, 3000 College Drive South, Lethbridge, AB T1K 1L6, Canada
Interests: actinobacteria; fungal endophytes; yeast; microscopic fungi; microalgae; cyanobacteria; lichens; alkaloids; terpenoids; aromatic; lipids; fatty acids; peptides; antitumor; antiviral
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Dear Colleagues,

Secondary metabolites are organic compounds that are not directly involved in the growth, development, or reproduction of an organism. Unlike primary metabolites, which are essential for basic life processes, secondary metabolites often confer adaptive roles that can help an organism to survive in its environment.

Secondary metabolites are incredibly diverse in structure and function, representing a wide variety of compounds that can be grouped into different classes based on their biosynthetic origins and chemical structures.

Many secondary metabolites play roles in defense against herbivores, pathogens, or competitors. Some act as attractants for pollinators or seed-dispersing animals. Others provide protection from UV radiation or assist with allelopathy (where a plant releases chemicals to inhibit the growth of nearby competing plants).

Classes of secondary metabolites, articles that are interesting for publication in this issue:

Alkaloids: Nitrogen-containing compounds that often have potent effects on animals. Examples include caffeine, nicotine, morphine, and quinine. Many are used as drugs or have pharmacological effects.

Terpenoids (or isoprenoids lipids): They comprise the largest class of secondary metabolites. Examples include steroids, carotenoids, and many essential oils.

Phenolic compounds: These include flavonoids, tannins, and lignins. They can have antioxidant properties and play a role in plant defense.

Polyketides: This diverse group includes many antibiotics, anticancer agents, and other bioactive compounds.

Pharmaceutical relevance: Due to their bioactivity, many secondary metabolites have been utilized in human medicine. For instance, the alkaloid compound salicylic acid, derived from willow bark, led to the development of aspirin. Many antibiotics are secondary metabolites produced by bacteria and fungi.

Ecological importance: Secondary metabolites play crucial roles in plant–plant, plant–animal, and plant–microbe interactions. They shape the dynamics of ecosystems, influencing feeding behaviors, mutualistic relationships, and competitive interactions.

Biotechnological applications: With advances in synthetic biology and metabolic engineering, there's growing interest in harnessing microbes like bacteria and yeast to produce valuable secondary metabolites, either by transferring the metabolic pathways from native producers or designing novel pathways.

In summary, while secondary metabolites are not required for the basic metabolic processes of an organism, they play significant roles in its interaction with the environment, defense, and survival and have vast importance for humans in terms of medicine, agriculture, and biotechnology.

Which symbionts produce secondary metabolites?

Many symbiotic organisms produce secondary metabolites that play roles in the mutualistic relationships that they establish. These compounds can have a wide range of functions, ranging from defense to communication. Some symbionts that produce secondary metabolites include:

Endophytic fungi: These are fungi that live inside plant tissues without causing any apparent harm. Many endophytes produce secondary metabolites that can protect the host plant from herbivores, pathogens, or environmental stresses. For example, some grass species harbor endophytic fungi that produce alkaloids toxic to grazing animals, providing the grass with a form of chemical defense.

Mycorrhizal fungi: These fungi form symbiotic associations with the roots of most plants, helping them to take up nutrients from the soil. In return, the plant provides the fungus with carbohydrates. Some of these fungi also produce secondary metabolites that can deter herbivores or protect against pathogens.

Rhizobia: These are nitrogen-fixing bacteria that form nodules on the roots of leguminous plants. While the primary role of rhizobia is to convert atmospheric nitrogen into a form usable by plants, they also produce secondary metabolites that might be involved in communication and establishing the symbiotic relationship.

Marine invertebrates and their microbial symbionts: Many marine organisms, such as sponges, corals, and ascidians, harbor microbial symbionts that produce a plethora of secondary metabolites. Some of these compounds deter predators, inhibit the growth of competing organisms, or protect against pathogens. Often, the exact producer (host or symbiont) of a particular secondary metabolite in these associations can be challenging to determine, but there's evidence that many of these compounds are synthesized by the microbial partners.

Leaf-cutter ants and their fungal cultivars: Leaf-cutter ants cultivate a particular type of fungus as their primary food source. In return, the fungus receives a steady supply of leaf material. Some secondary metabolites produced by the fungus protect the cultivar from parasitic fungi and other potential threats.

Lichens: Lichens are mutualistic associations between fungi and photosynthetic partners (algae or cyanobacteria). Many lichens produce secondary metabolites, visible as unique pigments or detected chemically, that might play roles in protection from UV radiation, herbivory, or microbial invasion.

These are just a few examples. The production of secondary metabolites in symbiotic relationships is widespread and represents a rich field of study, especially given the clear ecological and potential pharmacological importance of these compounds.

Prof. Dr. Valery M. Dembitsky
Guest Editor

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Keywords

  • microbial symbionts
  • plants
  • lichens, fungi
  • seaweeds
  • microalgae
  • marine invertebrates
  • secondary metabolites
  • human health
  • fungal endophytes
  • bacteria

Published Papers (2 papers)

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Research

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10 pages, 1419 KiB  
Communication
Comparative Analysis of Cyanotoxins in Fishponds in Nigeria and South Africa
by Odo J. Bassey, Jabulani R. Gumbo, Munyaradzi Mujuru, Adeeyo Adeyemi and Farai Dondofema
Microbiol. Res. 2024, 15(2), 447-456; https://doi.org/10.3390/microbiolres15020030 - 24 Mar 2024
Viewed by 526
Abstract
Over the decades, the aquaculture sector has witnessed substantial growth, contributing significantly to the nation’s economy. However, the menace of CyanoHABs threatens the sustainability of fish farming. Considering the possible hazards linked to cyanotoxins in food and water, a comparative study design between [...] Read more.
Over the decades, the aquaculture sector has witnessed substantial growth, contributing significantly to the nation’s economy. However, the menace of CyanoHABs threatens the sustainability of fish farming. Considering the possible hazards linked to cyanotoxins in food and water, a comparative study design between commercial fish in Nigeria and South Africa was employed to investigate cyanotoxins in the water from fishponds. Six commercial fishponds in Calabar Municipality—Nigeria and Duthuni—South Africa with varying climatic zones were selected. Water samples from the ponds were collected at intervals during different seasons (summer, winter, dry, and wet seasons) to capture climate-induced variation. Liquid chromatography–mass spectrometry (LCMS) in combination with the metabolites database was used for the identification of toxic cyanometabolites in water samples. The molecular networking approach, coupled with the Global Natural Products Social Molecular Networking (GNPS) database and CANOPUS annotation, enabled the putative identification of cyanometabolites. The resulting molecular network unveiled discernible clusters representing related molecule families, aiding in the identification of both known cyanotoxins and unfamiliar analogues. Furthermore, the molecular network revealed that water samples from different fishponds shared specific metabolites, including ethanesulfonic acid, pheophorbide A, cholic acid, phenylalanine, amyl amine, phosphocholine (PC), and sulfonic acid, despite variations in location, local climatic factors, and sampling sites. The fishponds in Nigeria showed the presence of multiple cyanotoxin classes in the dry, wet, and summer seasons in the water. Aflatoxin was identified in all sampling sites in Nigeria (N1, N2, and N3). The Duthuni, South Africa, sampling sites (P1, P2, and P3) exhibited the presence of microginins and microcystins. All the fishponds displayed a widespread occurrence of anabaenopeptins, aplysiatoxins, aflatoxin, microcolins, and marabmids during the selected summer. In conclusion, the untargeted metabolome analysis, guided by GNPS, proved highly effective in identifying both toxic and non-toxic metabolites in fishponds. Full article
(This article belongs to the Special Issue Bioactive Secondary Metabolites of Microbial Symbionts)
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25 pages, 3552 KiB  
Review
Bioactive Diepoxy Metabolites and Highly Oxygenated Triterpenoids from Marine and Plant-Derived Bacteria and Fungi
by Valery M. Dembitsky
Microbiol. Res. 2024, 15(1), 66-90; https://doi.org/10.3390/microbiolres15010005 - 21 Dec 2023
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Abstract
This article explores the diverse array of biologically active compounds derived from microbial symbionts, particularly focusing on the isolation and characterization of diepoxides, highly oxygenated triterpenoids, secosteroids, ergostane-type steroids, and meroterpenoids from various marine and plant-derived fungi. We highlight significant discoveries such as [...] Read more.
This article explores the diverse array of biologically active compounds derived from microbial symbionts, particularly focusing on the isolation and characterization of diepoxides, highly oxygenated triterpenoids, secosteroids, ergostane-type steroids, and meroterpenoids from various marine and plant-derived fungi. We highlight significant discoveries such as vitamin D variants from fungal species, unique sesterterpenoids from mangrove endophytic fungi, and secosteroids with potential medicinal applications. The study delves into the structural uniqueness and bioactivities of these compounds, including their anti-inflammatory, antibacterial, antifungal, antiviral, and cytotoxic effects. Notable findings include the isolation of compounds with significant activity against cancer cell lines, the inhibition of acetylcholinesterase, and promising antifouling properties. This work underscores the potential of microbial symbionts as a rich source of novel bioactive compounds with diverse therapeutic applications, highlighting the importance of marine and fungal biodiversity in drug discovery and development. Full article
(This article belongs to the Special Issue Bioactive Secondary Metabolites of Microbial Symbionts)
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