Strain DJ57T is a Gram-reaction-negative, filamentous-shaped, non-flagellated, aerobic bacterium isolated from farmland soil in Hunan province of China. 16S rRNA gene sequence analysis demonstrated that this isolate belonged to the genus Niastella, with 95.83 % nucleotide identity to Niastella populi THYL-44T, while the similarities to other type strains of species of the genus Niastella were less than 95.76 %. The major isoprenoid quinone was menaquinone-7 and the major fatty acids (>5 %) were iso-C15 : 0, iso-C17 : 0 3-OH, iso-C15 : 1 G, anteiso-C15 : 0 and iso-C16 : 0. The DNA G+C content was 44 mol%. Polar lipids were phosphatidylethanolamine, three unknown aminophospholipids, three unknown phospholipids and six unknown lipids. The chemotaxonomic, phenotypic and genotypic data indicated that strain DJ57T represents a novel species of the genus Niastella, for which the name Niastella vici sp. nov. is proposed. The type strain is DJ57T ( = KCTC 42474T = CCTCC AB 2015052T).
BernardetJ. F.,
NakagawaY.,
HolmesB.
Subcommittee on the taxonomy of Flavobacterium and Cytophaga-like bacteria of the International Committee on Systematics of Prokaryotes
2002; Proposed minimal standards for describing new taxa of the family Flavobacteriaceae and emended description of the family. Int J Syst Evol Microbiol 52:1049–1070
BowmanJ. P.2000; Description of Cellulophaga algicola sp. nov., isolated from the surfaces of Antarctic algae, and reclassification of Cytophaga uliginosa (ZoBell and Upham 1944) Reichenbach 1989 as Cellulophaga uliginosa comb. nov. Int J Syst Evol Microbiol 50:1861–1868[CrossRef]
CashionP.,
Holder-FranklinM. A.,
McCullyJ.,
FranklinM.1977; A rapid method for the base ratio determination of bacterial DNA. Anal Biochem 81:461–466 [View Article][PubMed]
KimuraM.1980; A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 16:111–120 [View Article][PubMed]
KroppenstedtR. M.1985; Fatty acid and menaquinone analysis of actinomycetes and related organisms. In Chemical Methods in Bacterial Systematics (Society for Applied Bacteriology Technical Series vol. 20) pp 173–199Edited byGoodfellowM.,
MinnikinD. E.
London: Academic Press;
MesbahM.,
PremachandranU.,
WhitmanW. B.1989; Precise measurement of the G+C conternt of deoxyribonucleic acid by high performance liquid chromatography. Int J Syst Bacteriol 39:159–167 [View Article]
ThompsonJ. D.,
GibsonT. J.,
PlewniakF.,
JeanmouginF.,
HigginsD. G.1997; The clustal_x windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25:4876–4882 [View Article][PubMed]
TindallB. J.1990; A comparative study of the lipid composition of Halobacterium saccharovorum from various sources. Syst Appl Microbiol 13:128–130 [View Article]
VentosaA.,
MarquezM. C.,
KocurM.,
TindallB. J.1993; Comparative study of Micrococcus sp. strains CCM 168 and CCM 1405 and members of the genus Salinicoccus
. Int J Syst Bacteriol 43:245–248 [View Article][PubMed]
WeonH. Y.,
KimB. Y.,
YooS. H.,
LeeS. Y.,
KwonS. W.,
GoS. J.,
StackebrandtE.2006; Niastella koreensis gen. nov., sp. nov. and Niastella yeongjuensis sp. nov., novel members of the phylum Bacteroidetes, isolated from soil cultivated with Korean ginseng. Int J Syst Evol Microbiol 56:1777–1782 [View Article][PubMed]
ZhangK.,
WangY.,
TangY.,
DaiJ.,
ZhangL.,
AnH.,
LuoG.,
RahmanE.,
FangC.2010; Niastella populi sp. nov., isolated from soil of Euphrates poplar (Populus euphratica) forest, and emended description of the genus Niastella
. Int J Syst Evol Microbiol 60:542–545 [View Article][PubMed]