Blastomonas fulva sp. nov., aerobic photosynthetic bacteria isolated from a Microcystis culture

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Title
Blastomonas fulva sp. nov., aerobic photosynthetic bacteria isolated from a Microcystis culture
Author(s)
Hyung Gwan LeeSo Ra Ko; Jun Woo Lee; C S Lee; Chi-Yong Ahn; Hee-Mock Oh; L Jin
Bibliographic Citation
International Journal of Systematic and Evolutionary Microbiology, vol. 67, no. 8, pp. 3071-3076
Publication Year
2017
Abstract
Two Gram-stain-negative, aerobic, non-motile, non-spore-forming and rod-shaped bacteria, designated strains T2T and T5, were isolated from a culture of Microcystis from Daejeon, Republic of Korea. Comparative 16S rRNA gene sequence studies placed the new isolates in the class Alphaproteobacteria and, notably, most closely related to Blastomonas aquatica PE 4-5T, Blastomonas natatoria DSM 3183T and Blastomonas ursincola KR-99T showing 99.4 %, 98.2% and 97.9% 16S rRNA gene sequence similarities, respectively. The two novel strains shared 100% similarity with each other. The cells of strains T2T and T5 formed yellow colonies on R2A agar and contained Q-10 as the only ubiquinone, sphingoglycolipid, phosphatidylethanolamine, phosphatidylcholine, and phosphatidylglycerol as major polar lipids, and C17 : 1ω6c, summed feature 8 (C18 : 1ω7c and/or C18 : 1ω6c), C17 : 1ω8c and C17 : 0 as the major fatty acids (>5 %). The DNA G+C content of the genomes was determined to be 64.2 mol% for strain T2T and 64.4 mol% for strain T5. The DNA-DNA hybridization values of strains T2T and T5 with B. Aquatica PE 4-5T, B. Natatoria DSM 3183T, and B. ursincola KR-99T were 19.7-42.4 %. Based on the combined genotypic and phenotypic data, we propose that strains T2T and T5 represent a novel species of the genus Blastomonas, for which the name Blastomonas fulvasp. Nov. is proposed. The type strain is T2T (=KCTC 42354T=JCM 30467T).
Keyword
BlastomonasBlastomonas fulvaMicrocystis cultureT2T5
ISSN
1466-5026
Publisher
Microbiology Soc
Full Text Link
http://dx.doi.org/10.1099/ijsem.0.002084
Type
Article
Appears in Collections:
Synthetic Biology and Bioengineering Research Institute > Cell Factory Research Center > 1. Journal Articles
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