Myxobacteria | |
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Myxococcus xanthus | |
Scientific classification | |
Domain: | Bacteria |
Phylum: | Myxococcota |
Class: | Myxococcia Waite et al. 2020 |
Order: | Myxococcales Tchan et al. 1948 |
Families & genera | |
Synonyms | |
"Myxococcidae" Cavalier-Smith 2020 |
The myxobacteria ("slime bacteria") are a group of bacteria that predominantly live in the soil and feed on insoluble organic substances. The myxobacteria have very large genomes relative to other bacteria, e.g. 9–10 million nucleotides except for Anaeromyxobacter and Vulgatibacter. One species of myxobacteria, Minicystis rosea, has the largest known bacterial genome with over 16 million nucleotides. The second largest is another myxobacteria Sorangium cellulosum.
Myxobacteria can move by gliding. They typically travel in swarms (also known as wolf packs), containing many cells kept together by intercellular molecular signals. Individuals benefit from aggregation as it allows accumulation of the extracellular enzymes that are used to digest food; this in turn increases feeding efficiency. Myxobacteria produce a number of biomedically and industrially useful chemicals, such as antibiotics, and export those chemicals outside the cell.
Myxobacteria are used to study the polysaccharide production in gram-negative bacteria like the model Myxococcus xanthus which have four different mechanisms of polysaccharide secretion and where a new Wzx/Wzy mechanism producing a new polysaccharide was identified in 2020.
Myxobacteria are also good models to study the multicellularity in the bacterial world.
Life cycle
When nutrients are scarce, myxobacterial cells aggregate into fruiting bodies (not to be confused with those in fungi), a process long-thought to be mediated by chemotaxis but now considered to be a function of a form of contact-mediated signaling. These fruiting bodies can take different shapes and colors, depending on the species. Within the fruiting bodies, cells begin as rod-shaped vegetative cells, and develop into rounded myxospores with thick cell walls. These myxospores, analogous to spores in other organisms, are more likely to survive until nutrients are more plentiful. The fruiting process is thought to benefit myxobacteria by ensuring that cell growth is resumed with a group (swarm) of myxobacteria, rather than as isolated cells. Similar life cycles have developed among certain amoebae, called cellular slime molds.
At a molecular level, initiation of fruiting body development in Myxococcus xanthus is regulated by Pxr sRNA.
Myxobacteria such as Myxococcus xanthus and Stigmatella aurantiaca are used as model organisms for the study of development.
Various myxobacterial species as sketched by Roland Thaxter in 1892: Chondromyces crocatus (figs. 1–11), Stigmatella aurantiaca (figs. 12–19 and 25-28), Melittangium lichenicola (figs. 20–23), Archangium gephyra (fig. 24), Myxococcus coralloides (figs. 29-33), Polyangium vitellinum (figs. 34-36), and Myxococcus fulvus (figs. 37-41). Thaxter was the first taxonomist to recognize the bacterial nature of the myxobacteria. Previously, they had been misclassified as members of the fungi imperfecti.It has been suggested that the last common ancestor of myxobacteria was an aerobe and that their anaerobic predecessors lived syntrophically with early eukaryotes.
Clinical use
Metabolites secreted by Sorangium cellulosum known as epothilones have been noted to have antineoplastic activity. This has led to the development of analogs which mimic its activity. One such analog, known as Ixabepilone is a U.S. Food and Drug Administration approved chemotherapy agent for the treatment of metastatic breast cancer.
Myxobacteria are also known to produce gephyronic acid, an inhibitor of eukaryotic protein synthesis and a potential agent for cancer chemotherapy.
Phylogeny
The currently accepted taxonomy is based on the List of Prokaryotic names with Standing in Nomenclature (LPSN) and National Center for Biotechnology Information (NCBI)
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See also
References
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- Hoshino, Y.; Gaucher, E.A. (2021). "Evolution of bacterial steroid biosynthesis and its impact on eukaryogenesis". PNAS. 118 (25): e2101276118. doi:10.1073/pnas.2101276118. ISSN 0027-8424. PMC 8237579. PMID 34131078.
- "FDA Approval for Ixabepilone". National Cancer Institute.
- Sasse F, Steinmetz H, Höfle G, Reichenbach H (January 1995). "Gephyronic acid, a novel inhibitor of eukaryotic protein synthesis from Archangium gephyra (myxobacteria). Production, isolation, physico-chemical and biological properties, and mechanism of action". J. Antibiot. 48 (1): 21–5. doi:10.7164/antibiotics.48.21. PMID 7868385.
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- Sayers; et al. "Deltaproteobacteria". National Center for Biotechnology Information (NCBI) taxonomy database. Retrieved 2022-09-09.
- "The LTP". Retrieved 20 November 2023.
- "LTP_all tree in newick format". Retrieved 20 November 2023.
- "LTP_08_2023 Release Notes" (PDF). Retrieved 20 November 2023.
- "GTDB release 08-RS214". Genome Taxonomy Database. Retrieved 10 May 2023.
- "bac120_r214.sp_label". Genome Taxonomy Database. Retrieved 10 May 2023.
- "Taxon History". Genome Taxonomy Database. Retrieved 10 May 2023.
External links
- The Myxobacteria Web Page
- Schwarmentwicklung und Morphogenese bei Myxobakterien on YouTube
- Myxobacteria form Fruiting Bodies on YouTube
- Myxococcus xanthus preying on an E. coli colony on YouTube
Prokaryotes: Bacteria classification | |||||||||||||||||||
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Terrabacteria BV1, BV3, BV5 |
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Thermotogida |
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Fusobacterida |
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Hydrobacteria BV2, BV4 |
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others |
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Taxon identifiers | |
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Myxococcales |