TY - JOUR
T1 - d-Tartrate utilization correlates with phylogenetic subclade in Pseudomonas cichorii
AU - Iiyama, Kazuhiro
AU - Tani, Sayo
AU - Yagi, Haruka
AU - Hashimoto, Sara
AU - Suga, Yasuhiro
AU - Tsuchiya, Kenichi
AU - Furuya, Naruto
N1 - Publisher Copyright:
© The Author(s) 2021. Published by Oxford University Press on behalf of FEMS.
PY - 2021/2/4
Y1 - 2021/2/4
N2 - Pseudomonas cichorii is divided into two subclades based on the 16S ribosomal RNA gene sequence and core genome multilocus sequence typing. It was shown that subclade 2 strains utilize d-tartrate as a sole carbon source, whereas subclade 1 strains do not. Draft genome sequencing was performed with P. cichorii strains to identify d-tartrate utilization genes. By genome comparative and homology search studies, an ∼7.1-kb region was identified to be involved in d-tartrate utilization. The region is subclade 2 specific, and contains tarD and dctA genes, which encode a putative enzyme and transporter of d-tartrate, respectively. When the region was introduced into subclade 1 strains, the transformants were able to utilize d-tartrate. Partial fragments of tarD and dctA were amplified from all subclade 2 strains tested in this study by PCR using gene-specific primers, but not from subclade 1 strains. This is the first report on the genetic analysis of biochemical characteristics corresponding to a specific phylogenetic group in P. cichorii.
AB - Pseudomonas cichorii is divided into two subclades based on the 16S ribosomal RNA gene sequence and core genome multilocus sequence typing. It was shown that subclade 2 strains utilize d-tartrate as a sole carbon source, whereas subclade 1 strains do not. Draft genome sequencing was performed with P. cichorii strains to identify d-tartrate utilization genes. By genome comparative and homology search studies, an ∼7.1-kb region was identified to be involved in d-tartrate utilization. The region is subclade 2 specific, and contains tarD and dctA genes, which encode a putative enzyme and transporter of d-tartrate, respectively. When the region was introduced into subclade 1 strains, the transformants were able to utilize d-tartrate. Partial fragments of tarD and dctA were amplified from all subclade 2 strains tested in this study by PCR using gene-specific primers, but not from subclade 1 strains. This is the first report on the genetic analysis of biochemical characteristics corresponding to a specific phylogenetic group in P. cichorii.
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U2 - 10.1093/femsle/fnaa223
DO - 10.1093/femsle/fnaa223
M3 - Article
C2 - 33386401
AN - SCOPUS:85102018377
SN - 0378-1097
VL - 368
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
IS - 2
ER -