Mitsuru Numata
National Institute of Technology and Evaluation
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Featured researches published by Mitsuru Numata.
Genome Announcements | 2015
Yoshiyuki Ohtsubo; Yuji Nagata; Mitsuru Numata; Kieko Tsuchikane; Akira Hosoyama; Atsushi Yamazoe; Masataka Tsuda; Nobuyuki Fujita; Fusako Kawai
ABSTRACT Sphingopyxis macrogoltabida strain 203, the type strain of the species, grew on polyethylene glycol (PEG) and has been deposited to the stock culture at the Biological Resource Center, National Institute of Technology and Evaluation (NITE), under the number NBRC 15033. Here, we report the complete genome sequence of strain NBRC 15033. Unfortunately, genes for PEG degradation were missing.
Genome Announcements | 2015
Yoshiyuki Ohtsubo; Yuji Nagata; Mitsuru Numata; Kieko Tsuchikane; Akira Hosoyama; Atsushi Yamazoe; Masataka Tsuda; Nobuyuki Fujita; Fusako Kawai
ABSTRACT Strain 113P3 was isolated from activated sludge and identified as a polyvinyl alcohol (PVA)-degrading Pseudomonas species; it was later reidentified as Sphingopyxis species. Only three genes are directly relevant to the metabolism of PVA and comprise the pva operon, which was deposited as accession no. AB190228. Here, we report the complete genome sequence of strain 113P3, which has been conserved as a stock culture (NBRC 111507) at the Biological Resource Center, National Institute of Technology and Evaluation (NITE) (Tokyo, Japan). The genome of strain 113P3 is composed of a 4.4-Mb circular chromosome and a 243-kb plasmid. The whole finishing was conducted in silico except for four PCRs. The sequence corresponding to AB190288 exists on the chromosome.
Genome Announcements | 2014
Takamasa Miura; Keiko Tsuchikane; Mitsuru Numata; Maiko Hashimoto; Akira Hosoyama; Shoko Ohji; Atsushi Yamazoe; Nobuyuki Fujita
ABSTRACT Alcanivorax sp. strain NBRC 101098 was isolated from seawater in Japan. Strain NBRC 101098 is able to degrade various types of n-alkanes. Here, we report the complete genome of strain NBRC 101098.
Contact Dermatitis | 2018
Mamiko Shono; Mitsuru Numata; Kazumi Sasaki
Solvent Orange 60 (SO 60) is a perinone-type oil-soluble plastic dye, and may cause allergic contact dermatitis when used in spectacle frames. In 1999, we reported the first male case, who had a strong positive patch test reaction to SO 60 1% pet. (1, 2). We since continued to patch test SO 60 in patients with suspected spectacle frame dermatitis, and encountered 4 female patients with positive reactions between 2009 and 2016, the latest of whom is presented here.
Journal of General and Applied Microbiology | 2016
Kenta Yonezuka; Naoto Araki; Jun Shimodaira; Shoko Ohji; Akira Hosoyama; Mitsuru Numata; Atsushi Yamazoe; Daisuke Kasai; Eiji Masai; Nobuyuki Fujita; Takayuki Ezaki; Masao Fukuda
Bacteria capable of degrading cis-dichloroethene (cDCE) were screened from cDCE-contaminated soil, and YKD221, a bacterial strain that exhibited a higher growth on minimal salt agar plates in the presence of cDCE than in the absence of cDCE, were isolated. Phylogenetic studies of the 16S rRNA as well as gyrB, rpoD, and recA in YKD221 indicated that this strain is closely related to the type strains of Pseudomonas plecoglossicida, monteilii, and putida. An average nucleotide identity analysis indicated that YKD221 is most closely related to P. putida strains, including the type strain, which suggests that YKD221 belongs to P. putida. Although the genome of YKD221 was very similar to that of P. putida F1, a toluene-degrading strain, the YKD221 genome has 15 single-nucleotide polymorphisms and 4 insertions compared with the F1 genome. YKD221 caused the release of sufficient chloride ions from cDCE to suggest that the strain is able to completely dechlorinate and degrade cDCE. YKD221 also degraded trichloroethene but was unable to degrade trans-dichloroethene and tetrachloroethene. The degradation activity of YKD221 was elevated after growth on toluene. Inactivation of todC1, which encodes for a large subunit of the catalytic terminal component in toluene dioxygenase, resulted in a complete loss of growth on toluene and cDCE degradation activity. This is the first evidence of the involvement of todC1C2BA-coded toluene dioxygenase in cDCE degradation. YKD221 did not appear to grow on cDCE in a minimal salt liquid medium. However, YKD221 did exhibit an enhanced increase in cell concentration and volume of cells during growth on minimal salt agar plates with cDCE when first grown in LB medium. This behavior appears to have led us to misinterpret our initial results on YKD221 as an indication of improved growth in the presence of cDCE.
Genome Announcements | 2015
Yoshiyuki Ohtsubo; Yuji Nagata; Mitsuru Numata; Kieko Tsuchikane; Akira Hosoyama; Atsushi Yamazoe; Masataka Tsuda; Nobuyuki Fujita; Fusako Kawai
ABSTRACT Strain EY-1 was isolated from a microbial consortium growing on a random polymer of ethylene oxide and propylene oxide. Strain EY-1 grew on polyethylene glycol and polypropylene glycol and identified as Sphingopyxis macrogoltabida. Here, we report the complete genome sequence of Sphingopyxis macrogoltabida EY-1. The genome of strain EY-1 is comprised of a 4.76-Mb circular chromosome, and five plasmids. The whole finishing was conducted in silico, with aids of computational tools GenoFinisher and AceFileViewer. Strain EY-1 is available from Biological Resource Center, National Institute of Technology and Evaluation (Tokyo, Japan) (NITE).
Contact Dermatitis | 2018
Atsuko Aizawa; Akiko Ito; Yukiko Masui; Kazumi Sasaki; Yutaka Ishimura; Mitsuru Numata; Riichiro Abe
Department of Dermatology, Niigata University School of Medicine, Niigata, Japan Nagata Clinic, Niigata, Japan National Institute of Technology and Evaluation, Tokyo, Japan Correspondence Dr Atsuko Aizawa, Department of Dermatology, Niigata University School of Medicine, 1 Asahimachidori, Chuouku. Niigata 951-8510, Japan. Email: [email protected]
Genome Announcements | 2016
Yoshiyuki Ohtsubo; Shouta Nonoyama; Yuji Nagata; Mitsuru Numata; Keiko Tsuchikane; Akira Hosoyama; Atsushi Yamazoe; Masataka Tsuda; Nobuyuki Fujita; Fusako Kawai
ABSTRACT We determined the complete genome sequence of Sphingopyxis macrogoltabida strain 203N, a polyethylene glycol degrader. Because the PacBio assembly (285× coverage) seemed to be full of nucleotide-level mismatches, the Newbler assembly of MiSeq mate-pair and paired-end data was used for finishing and the PacBio assembly was used as a reference. The PacBio assembly carried 414 nucleotide mismatches over 5,953,153 bases of the 203N genome.
Genome Announcements | 2016
Yoshiyuki Ohtsubo; Shouta Nonoyama; Yuji Nagata; Mitsuru Numata; Keiko Tsuchikane; Akira Hosoyama; Atsushi Yamazoe; Masataka Tsuda; Nobuyuki Fujita; Fusako Kawai
ABSTRACT The complete genome sequence of Sphingopyxis terrae strain 203-1, which is capable of growing on polyethylene glycol, was determined. The genome consisted of a chromosome with a size of 3.98 Mb and a plasmid with a size of 4,328 bp. The strain was deposited to the National Institute of Technology and Evaluation (Tokyo, Japan) under the number NBRC 111660.
Genome Announcements | 2015
Yoshiyuki Ohtsubo; Yuji Nagata; Mitsuru Numata; Kieko Tsuchikane; Akira Hosoyama; Atsushi Yamazoe; Masataka Tsuda; Nobuyuki Fujita; Fusako Kawai
ABSTRACT Microbacterium (formerly Corynebacterium) sp. No. 7 was isolated from activated sludge as a polypropylene glycol (PPG)-assimilating bacterial strain. Its oxidative PPG degradation has been proposed on the basis of PPG dehydrogenase activity and the metabolic products. Here, we report the complete genome sequence of Microbacterium sp. No. 7. The genome of the strain No. 7 is composed of a 4,599,046-bp circular chromosome and two linear plasmids. The whole finishing was conducted in silico with aids of the computational tools GenoFinisher and AceFileViewer. Strain No. 7 is available from the Biological Resource Center, National Institute of Technology and Evaluation (NITE) (Tokyo, Japan).