Title |
Sphingosinicella ginsenosidimutans sp. nov., with ginsenoside converting activity |
Author |
Jin-Kwang Kim1,2, Myung-Suk Kang3, Sung Chul Park1, Kyeng-Min Kim4, Kangduk Choi4, Min-Ho Yoon2, and Wan-Taek Im4,5* |
Address |
1KI for the Biocentury, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Republic of Korea, 2Department of Bio-Environmental Chemistry, College of Agriculture and Life Sciences, Chungnam National University, Daejeon 305-764, Republic of Korea, 3Microorganism Resources Division, National Institute of Biological Resources, Incheon 404-708, Republic of Korea, 4Graduate School of Future Convergence Technology, Genomic Informatics Center, Hankyong National University, Kyonggi-do 456-749, Republic of Korea, 5Department of Biotechnology, Hankyong National University, Kyonggi-do 456-749, Republic of Korea |
Bibliography |
Journal of Microbiology, 53(7),435-441, 2015,
|
DOI |
10.1007/s12275-015-5087-3
|
Key Words |
16S rRNA gene, polyphasic taxonomy, Sphingosinicella
ginsenosidimutans, ginsenoside |
Abstract |
The Gram-reaction-negative, strictly aerobic, non-motile, nonspore-
forming, and rod-shaped bacterial strain designated
BS11T was isolated from the compost and its taxonomic position
was investigated by using a polyphasic approach. Strain
BS11T grew optimally at 30?7캜 and at pH 7.0 in the absence
of NaCl on nutrient agar. Strain BS11T displayed ?glucosidase
activity that was responsible for its ability to transform
ginsenoside Rb1 (one of the dominant active components of
ginseng) to Rd. On the basis of 16S rRNA gene sequence
similarity, strain BS11T was shown to belong to the family
Sphingomonadaceae and was related to Sphingosinicella vermicomposti
YC7378T (96.3% sequence similarity), S. xenopeptidilytica
3-2W4T (96.2%), S. microcystinivorans Y2T
(96.1%), and S. soli KSL-125 T (95.9%). The G+C content of
the genomic DNA was 64.9%. The major menaquinone was
Q-10 and the major fatty acids were summed feature 7 (comprising
C18:1 ?c/?t/?2t; 40.6%), C16:0 (22.5%), C17:1 ?c
(13.7%) and C17:0 (9.1%). DNA and chemotaxonomic data
supported the affiliation of strain BS11T to the genus Sphingosinicella.
Strain BS11T could be differentiated genotypically
and phenotypically from the recognized species of the
genus Sphingosinicella. The novel isolate therefore represents
a novel species, for which the name Sphingosinicella
ginsenosidimutans sp. nov. is proposed, with the type strain
BS11T (=KACC 16619T =JCM 18201T). |