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Schumannella soli sp. nov., a novel actinomycete isolated from mangrove soil by in situ cultivation
A novel actinobacterial strain, designated 10F1D-1 T , was isolated from soil sample collected from Futian mangrove nature reserve, China using of the in situ cultivation technique. Preliminary analysis based on the 16S rRNA gene sequence revealed that strain 10F1D-1 T was the member of genus Schuma...
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Published in: | Antonie van Leeuwenhoek 2021-10, Vol.114 (10), p.1657-1667 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A novel actinobacterial strain, designated 10F1D-1
T
, was isolated from soil sample collected from Futian mangrove nature reserve, China using of the in situ cultivation technique. Preliminary analysis based on the 16S rRNA gene sequence revealed that strain 10F1D-1
T
was the member of genus
Schumannella
with sharing highest sequence similarity (99.7%) to
Schumannella luteola
DSM 23141
T
. Phylogenetic analyses based on 16S rRNA gene sequences and core proteome consistently exhibited that strain 10F1D-1
T
formed a monophyletic clade with
Schumannella luteola
DSM 23141
T
. Comparative genomic analyses clearly separated strain 10F1D-1
T
from the only species of the genus
Schumannella
based on average nucleotide identity (ANI), average amino acid identity (AAI) and digital DNA-DNA hybridization (dDDH) values below the thresholds for species delineation. The genome of strain 10F1D-1
T
contains the biosynthetic gene clusters for osmoprotectants to adapt to the salt environment of mangrove. Strain 10F1D-1
T
also contains the biosynthetic gene clusters for bioactive compounds as secondary metabolites. On the basis of the polyphasic analysis, strain 10F1D-1
T
is considered to represent a novel species of the genus
Schumannella
, for which the name
Schumannella soli
sp. nov. (type strain 10F1D-1
T
= CGMCC1.16699
T
= JCM 33146
T
) is proposed. |
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ISSN: | 0003-6072 1572-9699 |
DOI: | 10.1007/s10482-021-01631-6 |