Kocuria rhizophila: Difference between revisions
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''Kocuria rhizophila'' has a single circular genome with 2,697,540 bp[1]. This is a relatively small genome compared to other species in the order Actinomycetales[1]. ''K. rhizophila'' strain DC2201's G+C content is 71.16%[1]. It is predicted it's genome contains 2,357 genes which code for proteins, 87.7% of which have the same function as proteins in other Actinobacteria[1]. It's genome contains over 200 genes related to membrane transport which have been theorized to help the bacterium use the chemicals around plant roots.1 Gene analysis shows some ''K. rhizophila'' genes have homology with dormancy genes of the closely related bacterium ''M. luteus'' which would provide tolerance to stresses in its environment[1]. | ''Kocuria rhizophila'' has a single circular genome with 2,697,540 bp[1]. This is a relatively small genome compared to other species in the order Actinomycetales[1]. ''K. rhizophila'' strain DC2201's G+C content is 71.16%[1]. It is predicted it's genome contains 2,357 genes which code for proteins, 87.7% of which have the same function as proteins in other Actinobacteria[1]. It's genome contains over 200 genes related to membrane transport which have been theorized to help the bacterium use the chemicals around plant roots.1 Gene analysis shows some ''K. rhizophila'' genes have homology with dormancy genes of the closely related bacterium ''M. luteus'' which would provide tolerance to stresses in its environment[1]. | ||
==Cell Structure | ==Cell Structure and Metabolism== | ||
Interesting features of cell structure; how it gains energy; what important molecules it produces. | Interesting features of cell structure; how it gains energy; what important molecules it produces. | ||
Revision as of 20:45, 19 April 2022
Classification
Domain: Bacteria
Phylum: Actinomycetota
Class: Actinomycetia
Order: Micrococcales
Family: Micrococcaceae
Species
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NCBI Taxonomy: [1] |
Kocuria rhizophila
Description and Significance
Describe the appearance, habitat, etc. of the organism, and why you think it is important.
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Appearance
Appearing to have a rigid cell wall, Kocuria rhizophila is a Gram-positive cocci[8]. Arrangements of K. rhizophila come in pairs, shorts chains, tetrads, cubical packets of eight, and irregular clusters[8]. K. Rhizophila usually form 2-3 millimeter whitish, round, convex colonies on initial isolation[8]. After prolonged incubation, K. Rhizophila might develop a yellowish pigmentation[8,12]. Under strict aerobic conditions the colonies progress to be dull and creamy with a yellow tinge[12].
Use in laboratory testing
The Kocuria rhizophila strain ATCC 9341 has been used in quality control for sterility testing, as a test for the effectiveness of antibiotics and fungicides, and for doxycycline, tetracycline, and chloramphenicol susceptibility testing since 1966 under the designation Micrococcus luteus[4]. This designation was corrected to the current name Kocuria rhizophila in 2003, and its use in these forms has continued since the designation change[4].
Use in multi-metal contaminated soils
Application of Kocuria rhizophila alongside citric acid has been shown to facilitate metal extraction from soil by plants[3]. The level of metal extraction is most fit for removing multi-metal contamination from soils, and it has been demonstrated to be effective in accumulating Cd, Cr, Cu, and Ni in Glycine max[3].
Ionizing radiation resistance
The Kocuria rhizophila strain PT10 has been shown to be resistant to ionizing radiation, isolated from roots of Panicum turgidum from the Tunisian Sahara[6]. Study of the PT10 strain has allowed for identification of mechanisms that generate ionizing radiation resistance[6].
Salt stress tolerance
The Kocuria rhizophila strains Y1 and 14ASP have been shown to enhance salt stress tolerance in maize and Oxalis corniculata respectively[7,9]. The strain Y1 is able to tolerate up to 10% environmental NaCl, and it transfers this tolerance to maize when inoculated[7]. Inoculation with strain Y1 in maize is associated with increased salt stress tolerance, changes in presence of plant hormones IAA and ABA, and increased gene expression of antioxidant and salt tolerance genes[7].
Genome Structure
Describe the size and content of the genome. How many chromosomes? Circular or linear? Other interesting features? What is known about its sequence?
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Kocuria rhizophila has a single circular genome with 2,697,540 bp[1]. This is a relatively small genome compared to other species in the order Actinomycetales[1]. K. rhizophila strain DC2201's G+C content is 71.16%[1]. It is predicted it's genome contains 2,357 genes which code for proteins, 87.7% of which have the same function as proteins in other Actinobacteria[1]. It's genome contains over 200 genes related to membrane transport which have been theorized to help the bacterium use the chemicals around plant roots.1 Gene analysis shows some K. rhizophila genes have homology with dormancy genes of the closely related bacterium M. luteus which would provide tolerance to stresses in its environment[1].
Cell Structure and Metabolism
Interesting features of cell structure; how it gains energy; what important molecules it produces.
(editing in progress)
Cell structure
Kocuria rhizophila is a Gram-positive cocci morphology similar to Staphylococci[8]. It has cell structures which are potentially robust enough to be able to withstand some usually destructive organic compounds[10].
Metabolism
K. rhizophila has required strictly aerobic conditions to be successfully cultured[2]. However, gene analysis shows that it has the potential to grow under anaerobic conditions[1]. Analysis of K. rhizophila’s genome showed that it likely has catabolic pathways for several compounds produced during plant decomposition[1]. It is a chemoorganoheterotroph adapted to utilize the compounds available in the rhizosphere[1].
Ecology and Pathogenesis
Habitat; symbiosis; biogeochemical significance; contributions to environment.
If relevant, how does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.
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Habitat
Kocuria Rhizophila is adapted to live in is the rhizosphere, the soil surrounding plant roots[1]. K. rhizophila has been identified alongside and inside plant roots from a wide variety of environments including maize, Oxalis corniculata, Panicum turgidum, and Typha angustifolia[6,7,9,2]. K. rhizophila has been identified as a member of a marine biofilm on a ship hull[11]. TheK. rhizophila isolated from this biofilm produced EPS with a higher carbohydrate and protein content than the other bacteria isolated from the same biofilm[11]. It has also been identified in Domiati cheese, a type of soft white salty cheese, among other salt-tolerant bacteria[14].
Pathogenesis
While not classified as pathogenic, Kocuria rhizophila has been found to be an opportunistic pathogen in extremely rare cases. The isolation along with the significance of this bacteria warrants great caution[12]. While it’s presence does warrant caution, K. rhizophila’s residency does not confirm infection[12]. K. rhizophila is normal as a flora of skin and mucous membranes[12]. K. rhizophila is ignored as a contaminant by laboratories because it is considered as a non-pathogenic bacteria[12]. While it can be found in people and animals, the infection of K. rhizophila can cause symptoms of sepsis and acute pancreatitis[12,13].
Symbiosis
K. rhizophila has been shown to have mutualistic interactions with maize, Glycine max, and Oxalis corniculata.[3,6,7] In maize and Oxalis corniculata, K. rhizophila strains have been shown to increase the salt tolerance of these plants.[6,7] When inoculated with K. rhizophila these host species were able to have greater biomass soil with low levels of salt compared to non-inoculated specimens as well as being able to survive more extreme levels of salt in soil.[6,7] K. rhizophila inoculated Glycine max, alongside application of citric acid, was able to improve the survivability and biomass of Glycine max in multi-metal contaminated soils as well as facilitating the uptake of Cd, Cr, Cu, and Ni into Glycine max.[3]
References
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Author
Page authored by Timothy Biewer-Heisler, Joseph Bell, and Linnaea Awdey; students of Prof. Jay Lennon at IndianaUniversity.
