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Two bacterial strains, designated MA1002T and MA1003T, were isolated from the air-conditioning system of a car. Cells of both strains were Gram-reaction-positive, non-motile, non-spore-forming coccoids, catalase- and oxidase-positive and UV-radiation resistant. The major fatty acids of strain MA1002T were iso-C17 : 0 and iso-C15 : 0 and those of strain MA1003T were iso-C16 : 0 and iso-C16 : 1 H. The polar lipid profile of MA1002T contained phosphatidylethanolamine, two unidentified phosphoglycolipids, an unidentified phospholipid, an unidentified aminophospholipid, an unidentified aminolipid and an unidentified lipid. MA1003T had three unidentified phosphoglycolipids, six unidentified phospholipids, two unidentified glycolipids and two unidentified polar lipids as the polar lipids. The G+C contents of the genomic DNA of MA1002T and MA1003T were 70.5 and 76.0 mol%, respectively. MK-8 was the predominant respiratory quinone for both strains. 16S rRNA gene sequence analysis showed that strain MA1002T was phylogenetically related to Deinococcus apachensis DSM 19763T, D. geothermalis DSM 11300T, D. aerius TR0125T and D. aetherius ST0316T (92.9, 92.6, 92.0 and 91.9 % sequence similarity, respectively), and MA1003T showed the highest sequence similarity to Deinococcus hopiensis KR-140T (92.9 %) and D. xinjiangensis X-82T (91.4 %). The results of genotypic and phenotypic characterizations showed that both strains could be distinguished from phylogenetically related species, and that the strains represented novel species within the genus Deinococcus, for which we propose the names Deinococcus metallilatus sp. nov. (type strain MA1002T = KACC 17964T = NBRC 110141T) and Deinococcus carri sp. nov. (type strain is MA1003T = KACC 17965T = NBRC 110142T).
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