Corynebacterium

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Corynebacterium
"Corynebacterium ulcerans" colonies on a blood agar plate
blood agar
plate
Scientific classification Edit this classification
Domain: Bacteria
Phylum: Actinomycetota
Class: Actinomycetia
Order: Mycobacteriales
Family: Corynebacteriaceae
Lehmann and Neumann 1907 (Approved Lists 1980)[2]
Genus: Corynebacterium
Lehmann and Neumann 1896 (Approved Lists 1980)[1]
Type species
Corynebacterium diphtheriae
(Kruse 1886) Lehmann and Neumann 1896 (Approved Lists 1980)
Species

See text.

Synonyms
  • Bacterionema Gilmour et al. 1961 (Approved Lists 1980)
  • Caseobacter Crombach 1978 (Approved Lists 1980)
  • Turicella Funke et al. 1994

Corynebacterium (

aerobic. They are bacilli (rod-shaped), and in some phases of life they are, more specifically, club-shaped, which inspired the genus name (coryneform
means "club-shaped").

They are widely distributed in nature in the

human microbiota) and are mostly innocuous, most commonly existing in commensal relationships with their hosts.[3] Some, such as C. glutamicum, are commercially and industrially useful.[4][5][6][7] Others can cause human disease, including, most notably, diphtheria, which is caused by C. diphtheriae. As with various species of microbiota (including their relatives in the genera Arcanobacterium and Trueperella), they usually are not pathogenic, but can occasionally opportunistically capitalize on atypical access to tissues (via wounds) or weakened host defenses
.

Taxonomy

The genus Corynebacterium was created by Lehmann and Neumann in 1896 as a

Eubacteria with high G:C content, with close phylogenetic relationship to Arthrobacter, Mycobacterium, Nocardia, and Streptomyces.[8]

The term comes from

pathogenic; for example, C. diphtheriae would be excluded.[citation needed] The term diphtheroid comes from Greek διφθέρα, diphthérā 'prepared hide, leather'.[11][12]

Genomics

Comparative analysis of corynebacterial genomes has led to the identification of several

G+C content ranging from 46-74 mol%.[14]

Characteristics

The principal features of the genus Corynebacterium were described by Collins and Cummins, for Coryn Taylor in 1986.

chemoorganotrophs. They are pleomorphic through their lifecycles, they occur in various lengths, and they frequently have thickenings at either end, depending on the surrounding conditions.[17]

Some corynebacteria are

Cell wall

The

L-Rhap-(1 → 4)--D-GlcNAc-phosphate. These form a complex commonly seen in Corynebacterium species: the mycolyl-AG–peptidoglican (mAGP).[21] Unlike most corynebacteria, Corynebacterium kroppenstedtii does not contain mycolic acids.[22]

Culture

Corynebacteria grow slowly, even on enriched media. In nutritional requirements, all need

blood agar, and trypticase soy agar (TSA). They form small, grayish colonies with a granular appearance, mostly translucent, but with opaque centers, convex, with continuous borders.[16] The color tends to be yellowish-white in Loeffler's medium. In TSA, they can form grey colonies with black centers and dentated borders that either resemble flowers (C. gravis), continuous borders (C. mitis), or a mix between the two forms (C. intermedium).[citation needed
]

Habitat

Corynebacterium species occur commonly in nature in soil, water, plants, and food products.

birds, have been recently reported for Corynebacterium uropygiale.[19] Some species are known for their pathogenic effects in humans and other animals. Perhaps the most notable one is C. diphtheriae, which acquires the capacity to produce diphtheria toxin only after interacting with a bacteriophage.[23][24] Other pathogenic species in humans include: C. amycolatum, C. striatum, C. jeikeium, C. urealyticum, and C. xerosis;[25][26][27][28][29] all of these are important as pathogens in immunosuppressed patients. Pathogenic species in other animals include C. bovis and C. renale.[30] This genus has been found to be part of the human salivary microbiome.[31]

Role in disease

The most notable human infection is

transformed by a gene from the β prophage.[23][24]

Several species cause disease in animals, most notably C. pseudotuberculosis, which causes the disease

trichomycosis axillaris.[36] C. striatum may cause axillary odor.[37] C. minutissimum causes erythrasma
.

Industrial uses

Nonpathogenic species of Corynebacterium are used for important industrial applications, such as the production of amino acids[38] and nucleotides, bioconversion of steroids,[39] degradation of hydrocarbons,[40] cheese aging,[41] and production of enzymes.[42] Some species produce metabolites similar to antibiotics: bacteriocins of the corynecin-linocin type,[34][43][44] antitumor agents,[45] etc. One of the most studied species is C. glutamicum, whose name refers to its capacity to produce glutamic acid in aerobic conditions.[46]

L-Lysine production is specific to C. glutamicum in which core metabolic enzymes are manipulated through genetic engineering to drive metabolic flux towards the production of NADPH from the pentose phosphate pathway, and L-4-aspartyl phosphate, the commitment step to the synthesis of L-lysine, lysC, dapA, dapC, and dapF. These enzymes are up-regulated in industry through genetic engineering to ensure adequate amounts of lysine precursors are produced to increase metabolic flux. Unwanted side reactions such as threonine and asparagine production can occur if a buildup of intermediates occurs, so scientists have developed mutant strains of C. glutamicum through PCR engineering and chemical knockouts to ensure production of side-reaction enzymes are limited. Many genetic manipulations conducted in industry are by traditional cross-over methods or inhibition of transcriptional activators.[47]

Expression of functionally active human

secretory pathway or the twin-arginine translocation pathway.[49]

Unlike gram-negative bacteria, the gram-positive Corynebacterium species lack

]

Species

Corynebacterium comprises the following species:[50]

References

  1. ^ Lehmann KB, Neumann R (1896). Atlas und Grundriss der Bakteriologie und Lehrbuch der speziellen bakteriologischen Diagnostik [Atlas and outline of bacteriology and textbook of special bacteriological diagnostics] (1st ed.). München: J.F. Lehmann.
  2. ^ Lehmann KB, Neumann R (1907). Lehmann's Medizin, Handatlanten X. Atlas und Grundriss der Bakteriologie und Lehrbuch der speziellen bakteriologischen Diagnostik [Lehmann's Medicine, Handbook X. Atlas and outline of bacteriology and textbook of special bacteriological diagnostics] (4th ed.). Munchen: J. F. Lehmann.
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  10. ^ βακτήριον, βακτηρία in Liddell and Scott.
  11. ^ διφθέρα in Liddell and Scott.
  12. ^ Harper, Douglas. "diphtheria". Online Etymology Dictionary.
  13. PMID 22390973
    .
  14. ^ Bernard, K.A.; Funke, G. (2012). "Genus I. Corynebacterium". In Goodfellow, M.; Kampfer, P.; Busse, H.J.; Trujillo, M.E.; Suzuki, K.; Ludwig, W.; Whitman, W.B. (eds.). Bergey's Manual of Systematic Bacteriology (2nd ed.). Springer. p. 245.
  15. ^ a b Collins, M. D.; Cummins, C. S. (1986). "Genus Corynebacterium Lehmann and Neumann 1896, 350AL". In Sneath, P. H. A.; Mair, N. S.; Sharpe, M. E.; Holt, J. G. (eds.). Bergey's Manual of Systematic Bacteriology. Vol. 2. Baltimore: Williams & Wilkins. pp. 1266–76.
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  24. ^ a b SIB: Viral exotoxin. Expasy: ViralZone. Accessed 2 Feb 2021
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  32. ^ "Difteria: MedlinePlus enciclopedia médica". www.nlm.nih.gov.
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  36. ^ Trichomycosis axillaris at eMedicine
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  38. ^ Yamada, K.; Kinoshita, S.; Tsunoda, T.; Aida, K., eds. (1972). The Microbial Production of Amino Acids. New York: Wiley.
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  50. ^ Euzéby JP, Parte AC. "Corynebacterium". List of Prokaryotic names with Standing in Nomenclature (LPSN). Retrieved June 21, 2022.

Further reading