Keiko Tsuchikane
National Institute of Technology and Evaluation
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Publication
Featured researches published by Keiko Tsuchikane.
Biotechnology for Biofuels | 2015
Noppon Lertwattanasakul; Tomoyuki Kosaka; Akira Hosoyama; Yutaka Suzuki; Nadchanok Rodrussamee; Minenosuke Matsutani; Masayuki Murata; Naoko Fujimoto; Suprayogi; Keiko Tsuchikane; Savitree Limtong; Nobuyuki Fujita; Mamoru Yamada
BackgroundHigh-temperature fermentation technology with thermotolerant microbes has been expected to reduce the cost of bioconversion of cellulosic biomass to fuels or chemicals. Thermotolerant Kluyveromyces marxianus possesses intrinsic abilities to ferment and assimilate a wide variety of substrates including xylose and to efficiently produce proteins. These capabilities have been found to exceed those of the traditional ethanol producer Saccharomyces cerevisiae or lignocellulose-bioconvertible ethanologenic Scheffersomyces stipitis.ResultsThe complete genome sequence of K. marxianus DMKU 3-1042 as one of the most thermotolerant strains in the same species has been determined. A comparison of its genomic information with those of other yeasts and transcriptome analysis revealed that the yeast bears beneficial properties of temperature resistance, wide-range bioconversion ability, and production of recombinant proteins. The transcriptome analysis clarified distinctive metabolic pathways under three different growth conditions, static culture, high temperature, and xylose medium, in comparison to the control condition of glucose medium under a shaking condition at 30°C. Interestingly, the yeast appears to overcome the issue of reactive oxygen species, which tend to accumulate under all three conditions.ConclusionsThis study reveals many gene resources for the ability to assimilate various sugars in addition to species-specific genes in K. marxianus, and the molecular basis of its attractive traits for industrial applications including high-temperature fermentation. Especially, the thermotolerance trait may be achieved by an integrated mechanism consisting of various strategies. Gene resources and transcriptome data of the yeast are particularly useful for fundamental and applied researches for innovative applications.
Genome Announcements | 2014
Shoko Ohji; Atsushi Yamazoe; Akira Hosoyama; Keiko Tsuchikane; Takayuki Ezaki; Nobuyuki Fujita
ABSTRACT Pseudomonas putida has attracted much interest for its environmental, industrial, biotechnological, and clinical importance. Here, we report the complete genome sequence of the type strain P. putida NBRC 14164. This genome sequence will assist to further elucidate the molecular mechanisms of the characteristic traits among strains belonging to the species P. putida.
Genome Announcements | 2013
Masaki Shintani; Akira Hosoyama; Shoko Ohji; Keiko Tsuchikane; Hiromi Takarada; Atsushi Yamazoe; Nobuyuki Fujita; Hideaki Nojiri
ABSTRACT Pseudomonas resinovorans strain CA10 can grow on carbazole as its sole carbon and nitrogen source. Here, we report the complete nucleotide sequence of the CA10 genome (a 6,285,863-bp chromosome and a 198,965-bp plasmid). CA10 carries a larger number of genes that are potentially responsible for aromatic hydrocarbon metabolism than do other previously sequenced Pseudomonas spp.
Microbiology and Immunology | 2016
Hiroyuki Hata; Tatsuya Natori; Takuya Mizuno; Izumi Kanazawa; Ibrahim Eldesouky; Masahiro Hayashi; Machiko Miyata; Hajime Fukunaga; Shoko Ohji; Akira Hosoyama; Eiji Aono; Atsushi Yamazoe; Keiko Tsuchikane; Nobuyuki Fujita; Takayuki Ezaki
Multilocus sequence analysis based on hypervariable housekeeping proteins was utilized to differentiate closely related species in the family Enterobacteriaceae. Of 150 housekeeping proteins, the top 10 hypervariable proteins were selected and concatenated to obtain distance data. Distances between concatenated proteins within the family were 0.9–41.2%, whereas the 16S rRNA and atpD‐gyrB‐infB‐rpoB concatenated sequence (4MLSA) distances were 0.8–6.0% and 0.9–22.1%, respectively. These data indicate that phylogenetic analysis by concatenation of hypervariable proteins is a powerful tool for discriminating species in the family Enterobacteriaceae. To confirm the discriminatory power of the 10 chosen concatenated hypervariable proteins (C10HKP), phylogenetic trees based on C10HKP, 4MLSA, and the 16S rRNA gene were constructed. Comparison of average bootstrap values among C10HKP, 4MLSA and 16S rRNA genes indicated that the C10HKP tree was the most reliable. Location via the C10HKP tree was consistent with existing assignments for almost all species in the family Enterobacteriaceae. However, the C10HKP tree suggested that several species (including Enterobacter massiliensis, Escherichia vulneris, Escherichia hermannii, and Salmonella subterranea) should be reassigned to different clusters than those defined in previous analyses. Furthermore, E. hermannii and S. subterranea appeared to fall onto a branch independent from those occupied by the other Enterobacteriaceae. Therefore, we propose Atlantibacter gen. nov., such that E. hermannii and S. subterranea would be transferred to genus Atlantibacter as Atlantibacter hermannii, comb. nov. and Atlantibacter subterranea. comb. nov., respectively.
Genome Announcements | 2014
Kohei Fukuda; Akira Hosoyama; Keiko Tsuchikane; Shoko Ohji; Atsushi Yamazoe; Nobuyuki Fujita; Masaki Shintani; Kazuhide Kimbara
ABSTRACT Comamonas testosteroni TK102 (NBRC 109938; JCM 19603) can utilize biphenyl as a sole carbon source and degrade polychlorinated biphenyls (PCBs). The complete nucleotide sequence of the TK102 genome was determined. TK102 possesses several integrative and conjugative element-like regions, and one of them carries biphenyl-degradative genes.
Genome Announcements | 2015
Takamasa Miura; Yoshihito Uchino; Keiko Tsuchikane; Yoshiyuki Ohtsubo; Shoko Ohji; Akira Hosoyama; Masako Ito; Yoh Takahata; Atsushi Yamazoe; Ken-ichiro Suzuki; Nobuyuki Fujita
ABSTRACT Sulfurospirillum strains UCH001 and UCH003 were isolated from anaerobic cis-1,2-dichloroethene-dechlorinating microbial consortia derived from groundwater in Japan. Here, we report the complete genome sequences of strains UCH001 and UCH003.
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.
Genome Announcements | 2014
LiiMien Yee; Akira Hosoyama; Shoko Ohji; Keiko Tsuchikane; Jun Shimodaira; Atsushi Yamazoe; Nobuyuki Fujita; Chiho Suzuki-Minakuchi; Hideaki Nojiri
ABSTRACT Acinetobacter guillouiae strain 20B can utilize dimethyl sulfide (DMS) as the sole sulfur source and degrade chloroethylenes. We report here the complete 4,648,418-bp genome sequence for this strain, which contains 4,367 predicted coding sequences (CDSs), including a well-characterized DMS degradative operon.
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.