Updated on 2026/04/03

写真a

 
NONOYAMA SHOUTA
 
Organization
School of Life Science and Technology Assistant Professor
Title
Assistant Professor
External link

Degree

  • 博士(生命科学) ( 東北大学 )

Research Areas

  • Life Science / Molecular biology

  • Life Science / Applied microbiology

Education

  • Tohoku University   Graduate School of Life Sciences

    2017.4 - 2020.7

      More details

  • Tohoku University   Graduate School of Life Sciences

    2015.4 - 2017.3

      More details

  • Ehime University   Faculty of Engineering

    2011.4 - 2015.3

      More details

Research History

  • Institute of Science Tokyo   School of Life Science and Technology   Assistant Professor

    2024.10

      More details

  • Tokyo Institute of Technology   School of Life Science and Technology   Assistant Professor

    2023.11 - 2024.9

      More details

  • Tokyo Institute of Technology   School of Life Science and Technology

    2022.4 - 2023.10

      More details

  • 東北大学大学院   生命科学研究科   特任研究員

    2022.1 - 2022.3

      More details

  • Tohoku University   Graduate School of Life Sciences

    2020.7 - 2021.12

      More details

Professional Memberships

Papers

  • The roles of hydrogen sulfide and reactive sulfur species in bacterial life within the human body. Reviewed International journal

    Shouta Nonoyama, Takayuki Shimizu, Shinji Masuda

    Nitric oxide : biology and chemistry   162   1 - 8   2026.2

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    We summarize current knowledge on the roles of hydrogen sulfide (H2S) and reactive sulfur species (RSS) in bacterial strategies for survival and colonizing within the human body. Bacteria inhabiting the human body utilize H2S, derived from their host environment, as an electron donor or signaling molecule, while others generate and directly use H2S through the metabolism of sulfur-containing organic and inorganic compounds. The intracellular levels of H2S and RSS are tightly controlled by various mechanisms, enabling bacteria to acquire antibiotic resistance and obtain iron from their hosts. These processes are driven by transcription factors that specifically sense RSS, some of which are derived from H2S. The polysulfidation of specific cysteine residues in these transcription factors plays a key role in regulating the expression of related genes, thereby governing the interactions between bacteria and their hosts. The synthesis of H2S and RSS by bacteria not only affects their pathogenicity but can also influence overall health of the human host.

    DOI: 10.1016/j.niox.2026.02.002

    PubMed

    researchmap

  • Giant linear plasmids in Mycobacterium avium harbour a tRNA array unit. Reviewed

    Yano H, Arikawa K, Ikeda H, Nonoyama S, Maruyama F, Kitada S, Kida H, Ato M, Iwamoto T, Nishiuchi Y

    DNA research : an international journal for rapid publication of reports on genes and genomes   2026.1

     More details

    Publishing type:Research paper (scientific journal)  

    Nontuberculous mycobacteria occasionally harbour clustered tRNA genes, referred to as a tRNA array unit, which is considered a putative antidefense system within their genomes. However, the precise genomic location of these tRNA array units remains unclear. To address this, we sequenced the complete genomes of 5 Mycobacterium avium strains carrying a tRNA array unit using a hybrid assembly of long and short reads followed by manual curation. The assemblies indicated that each strain harbours 3 to 5 extrachromosomal elements. In all genomes, the tRNA array unit was found on a linear contig exceeding 300 kb. Pulse-field gel electrophoresis (PFGE) and sodium dodecyl sulphate-PFGE revealed that the strains harbour linear plasmids corresponding to these large contigs with protein-capped termini. These linear plasmids encode a hybrid type VII/type IV secretion system but lack relaxase genes, which are typically present in mycobacterial circular plasmids. Additionally, they contain approximately 415 bp inverted repeats at the termini. Sequences of related plasmids were identified exclusively in the genomes of M. avium isolates from Japan available in public databases, suggesting a possible Asian origin. This study provides the first experimental evidence that M. avium harbours giant invertron-type linear plasmids carrying a tRNA array unit.

    DOI: 10.1093/dnares/dsaf039

    PubMed

    researchmap

  • Increased intracellular H2S levels enhance iron uptake in Escherichia coli. Reviewed International journal

    Shouta Nonoyama, Shintaro Maeno, Yasuhiro Gotoh, Ryota Sugimoto, Kan Tanaka, Tetsuya Hayashi, Shinji Masuda

    mBio   e0199124   2024.9

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    UNLABELLED: We investigated the impact of intracellular hydrogen sulfide (H2S) hyperaccumulation on the transcriptome of Escherichia coli. The wild-type (WT) strain overexpressing mstA, encoding 3-mercaptopyruvate sulfur transferase, produced significantly higher H2S levels than the control WT strain. The mstA-overexpressing strain exhibited increased resistance to antibiotics, supporting the prior hypothesis that intracellular H2S contributes to oxidative stress responses and antibiotic resistance. RNA-seq analysis revealed that over 1,000 genes were significantly upregulated or downregulated upon mstA overexpression. The upregulated genes encompassed those associated with iron uptake, including siderophore synthesis and iron import transporters. The mstA-overexpressing strain showed increased levels of intracellular iron content, indicating that H2S hyperaccumulation affects iron availability within cells. We found that the H2S-/supersulfide-responsive transcription factor YgaV is required for the upregulated expression of iron uptake genes in the mstA-overexpression conditions. These findings indicate that the expression of iron uptake genes is regulated by intracellular H2S, which is crucial for oxidative stress responses and antibiotic resistance in E. coli. IMPORTANCE: H2S is recognized as a second messenger in bacteria, playing a vital role in diverse intracellular and extracellular activities, including oxidative stress responses and antibiotic resistance. Both H2S and iron serve as essential signaling molecules for gut bacteria. However, the intricate intracellular coordination between them, governing bacterial physiology, remains poorly understood. This study unveils a close relationship between intracellular H2S accumulation and iron uptake activity, a relationship critical for antibiotic resistance. We present additional evidence expanding the role of intracellular H2S synthesis in bacterial physiology.

    DOI: 10.1128/mbio.01991-24

    PubMed

    researchmap

  • Evolution of the Tn4371 ICE family: traR-mediated coordination of cargo gene upregulation and horizontal transfer. Reviewed International journal

    Satoshi Matsumoto, Kouhei Kishida, Shouta Nonoyama, Keiichiro Sakai, Masataka Tsuda, Yuji Nagata, Yoshiyuki Ohtsubo

    Microbiology spectrum   e0060724   2024.9

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    ICEKKS102Tn4677 carries a bph operon for the mineralization of polychlorinated biphenyls (PCBs)/biphenyl and belongs to the Tn4371 ICE (integrative and conjugative element) family. In this study, we investigated the role of the traR gene in ICE transfer. The traR gene encodes a LysR-type transcriptional regulator, which is conserved in sequence, positioning, and directional orientation among Tn4371 family ICEs. The traR belongs to the bph operon, and its overexpression on solid medium resulted in modest upregulation of traG (threefold), marked upregulation of xis (80-fold), enhanced ICE excision and, most notably, ICE transfer frequency. We propose the evolutional roles of traR, which upon insertion to its current position, might have connected the cargo gene activation and ICE transfer. This property of ICE, i.e., undergoing transfer under environmental conditions that lead to cargo gene activation, would instantly confer fitness advantages to bacteria newly acquiring this ICE, thereby resulting in efficient dissemination of the Tn4371 family ICEs.IMPORTANCEOnly ICEKKS102Tn4677 is proven to transfer among the widely disseminating Tn4371 family integrative and conjugative elements (ICEs) from β and γ-proteobacteria. We showed that the traR gene in ICEKKS102Tn4677, which is conserved in the ICE family with fixed location and direction, is co-transcribed with the cargo gene and activates ICE transfer. We propose that capturing of traR by an ancestral ICE to the current position established the Tn4371 family of ICEs. Our findings provide insights into the evolutionary processes that led to the widespread distribution of the Tn4371 family of ICEs across bacterial species.

    DOI: 10.1128/spectrum.00607-24

    PubMed

    researchmap

  • A transcriptional regulator, IscR, of Burkholderia multivorans acts as both repressor and activator for transcription of iron-sulfur cluster-biosynthetic isc operon. Reviewed International journal

    Shouta Nonoyama, Kouhei Kishida, Keiichiro Sakai, Yuji Nagata, Yoshiyuki Ohtsubo, Masataka Tsuda

    Research in microbiology   171 ( 8 )   319 - 330   2020.7

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    Bacterial iron-sulfur (Fe-S) clusters are essential cofactors for many metabolic pathways, and Fe-S cluster-containing proteins (Fe-S proteins) regulate the expression of various important genes. However, biosynthesis of such clusters has remained unknown in genus Burkholderia. Here, we clarified that Burkholderia multivorans ATCC 17616 relies on the ISC system for the biosynthesis of Fe-S clusters, and that the biosynthetic genes are organized as an isc operon, whose first gene encodes IscR, a transcriptional regulatory Fe-S protein. Transcription of the isc operon was repressed and activated under iron-rich and -limiting conditions, respectively, and Fur, an iron-responsive global transcriptional regulator, was indicated to indirectly regulate the expression of isc operon. Further analysis using a ΔiscR mutant in combination with a constitutive expression system of IscR and its derivatives indicated transcriptional repression and activation of isc operon by holo- and apo-forms of IscR, respectively, through their binding to the sequences within an isc promoter-containing (Pisc) fragment. Biochemical analysis using the Pisc fragment suggested that the apo-IscR binding sequence differs from the holo-IscR binding sequence. The results obtained in this study revealed a unique regulatory system for the expression of the ATCC 17616 isc operon that has not been observed in other genera.

    DOI: 10.1016/j.resmic.2020.06.005

    PubMed

    researchmap

  • Conjugative Transfer of IncP-9 Catabolic Plasmids Requires a Previously Uncharacterized Gene, mpfK, Whose Homologs Are Conserved in Various MPFT-Type Plasmids. Reviewed International journal

    Kouhei Kishida, Shouta Nonoyama, Tim Lukas, Shotaro Kawahara, Koji Kudo, Yuji Nagata, Yoshiyuki Ohtsubo, Masataka Tsuda

    Applied and environmental microbiology   85 ( 24 )   2019.12

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    Conjugative transfer of bacterial plasmids to recipient cells is often mediated by type IV secretion machinery. Experimental investigations into the minimal gene sets required for efficient conjugative transfer suggest that such gene sets are variable, depending on plasmids. We have been analyzing the conjugative transfer of Pseudomonas-derived and IncP-9 plasmids, NAH7 and pWW0, whose conjugation systems belong to the MPFT type. Our deletion analysis and synthetic biology analysis in this study showed that these plasmids require previously uncharacterized genes, mpfK (formerly orf34) and its functional homolog, kikA, respectively, for their efficient conjugative transfer. MpfK was localized in periplasm and had four cysteine residues whose intramolecular or intermolecular disulfide bond formation was suggested to be important for efficient conjugative transfer. The mpfK homologs were specifically carried by many MPFT-type plasmids, including non-IncP-9 plasmids, such as R388 and R751. Intriguingly, the mpfK homologs from the two non-IncP-9 plasmids were not required for conjugation of their plasmids, but were able to complement efficiently the transfer defect of the NAH7 mpfK mutant. Our results suggested the importance of the mpfK homologs for conjugative transfer of MPFT-type plasmids.IMPORTANCE IncP-9 plasmids are important mobile genetic elements for the degradation of various aromatic hydrocarbons. Elucidation of conjugative transfer of such plasmids is expected to greatly contribute to our understanding of its role in the bioremediation of polluted environments. The present study mainly focused on the conjugation system of NAH7, a well-studied and naphthalene-catabolic IncP-9 plasmid. Our analysis showed that the NAH7 conjugation system uniquely requires, in addition to the conserved components of the type IV secretion system (T4SS), a previously uncharacterized periplasmic protein, MpfK, for successful conjugation. Our findings collectively revealed a unique type of T4SS-associated conjugation system in the IncP-9 plasmids.

    DOI: 10.1128/AEM.01850-19

    PubMed

    researchmap

  • The Small Protein HemP Is a Transcriptional Activator for the Hemin Uptake Operon in Burkholderia multivorans ATCC 17616. Reviewed International journal

    Takuya Sato, Shouta Nonoyama, Akane Kimura, Yuji Nagata, Yoshiyuki Ohtsubo, Masataka Tsuda

    Applied and environmental microbiology   83 ( 16 )   2017.8

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    Iron and heme play very important roles in various metabolic functions in bacteria, and their intracellular homeostasis is maintained because high concentrations of free forms of these molecules greatly facilitate the Fenton reaction-mediated production of large amounts of reactive oxygen species that severely damage various biomolecules. The ferric uptake regulator (Fur) from Burkholderiamultivorans ATCC 17616 is an iron-responsive global transcriptional regulator, and its fur deletant exhibits pleiotropic phenotypes. In this study, we found that the phenotypes of the fur deletant were suppressed by an additional mutation in hemP The transcription of hemP was negatively regulated by Fur under iron-replete conditions and was constitutive in the fur deletant. Growth of a hemP deletant was severely impaired in a medium containing hemin as the sole iron source, demonstrating the important role of HemP in hemin utilization. HemP was required as a transcriptional activator that specifically binds the promoter-containing region upstream of a Fur-repressive hmuRSTUV operon, which encodes the proteins for hemin uptake. A hmuR deletant was still able to grow using hemin as the sole iron source, albeit at a rate clearly lower than that of the wild-type strain. These results strongly suggested (i) the involvement of HmuR in hemin uptake and (ii) the presence in ATCC 17616 of at least part of other unknown hemin uptake systems whose expression depends on the HemP function. Our in vitro analysis also indicated high-affinity binding of HemP to hemin, and such a property might modulate transcriptional activation of the hmu operon.IMPORTANCE Although the hmuRSTUV genes for the utilization of hemin as a sole iron source have been identified in a few Burkholderia strains, the regulatory expression of these genes has remained unknown. Our analysis in this study using B. multivorans ATCC 17616 showed that its HemP protein is required for expression of the hmuRSTUV operon, and the role of HemP in betaproteobacterial species was elucidated for the first time, to our knowledge, in this study. The HemP protein was also found to have two additional properties that have not been reported for functional homologues in other species; one is that HemP is able to bind to the promoter-containing region of the hmu operon to directly activate its transcription, and the other is that HemP is also required for the expression of an unknown hemin uptake system.

    DOI: 10.1128/AEM.00479-17

    PubMed

    researchmap

  • Complete genome sequence of Burkholderia caribensis Bcrs1W (NBRC110739), a strain co-residing with phenanthrene degrader Mycobacterium sp. EPa45. Reviewed International journal

    Yoshiyuki Ohtsubo, Shouta Nonoyama, Natsumi Ogawa, Hiromi Kato, Yuji Nagata, Masataka Tsuda

    Journal of biotechnology   228   67 - 68   2016.6

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    Complete genome sequence of Burkholderia caribensis Bcrs1W, isolated from a phenanthrene-degrading mixed culture, was determined. The genomic information of Bcrs1W will be beneficial to elucidating the mechanisms of its positive effects on phenanthrene degradation by co-residing Mycobacterium sp. Epa45, and to exploiting their degradation potentials.

    DOI: 10.1016/j.jbiotec.2016.04.042

    PubMed

    researchmap

  • Complete Genome Sequence of Sphingopyxis terrae Strain 203-1 (NBRC 111660), a Polyethylene Glycol Degrader. Reviewed International journal

    Yoshiyuki Ohtsubo, Shouta Nonoyama, Yuji Nagata, Mitsuru Numata, Keiko Tsuchikane, Akira Hosoyama, Atsushi Yamazoe, Masataka Tsuda, Nobuyuki Fujita, Fusako Kawai

    Genome announcements   4 ( 3 )   2016.6

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    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.

    DOI: 10.1128/genomeA.00530-16

    PubMed

    researchmap

  • Complete Genome Sequence of Sphingopyxis macrogoltabida Strain 203N (NBRC 111659), a Polyethylene Glycol Degrader. Reviewed International journal

    Yoshiyuki Ohtsubo, Shouta Nonoyama, Yuji Nagata, Mitsuru Numata, Keiko Tsuchikane, Akira Hosoyama, Atsushi Yamazoe, Masataka Tsuda, Nobuyuki Fujita, Fusako Kawai

    Genome announcements   4 ( 3 )   2016.6

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    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.

    DOI: 10.1128/genomeA.00529-16

    PubMed

    researchmap

▼display all

MISC

  • Analysis of Transcriptional activation involved in iron-sulfur cluster biogenesis operon in Burkholderia multivorans

    野々山翔太, 岸田康平, 酒井啓一郎, 永田裕二, 津田雅孝, 大坪嘉行

    日本農芸化学会大会講演要旨集(Web)   2021   2021

  • Analysis of Transcriptional activation involved in iron-sulfur cluster biogenesis operon in Burkholderia multivorans

    野々山翔太, 岸田康平, 永田裕二, 大坪嘉行, 津田雅孝

    日本農芸化学会大会講演要旨集(Web)   2020   2020

  • Burkholderia属細菌における鉄硫黄クラスター生合成系の転写制御機構の解析

    野々山翔太, 岸田康平, 永田裕二, 大坪嘉行, 津田雅孝

    日本農芸化学会大会講演要旨集(Web)   2019   2019

  • Mycobacterium sp.EPa45株におけるフェナントレン分解遺伝子群の転写解析

    市橋永吉, 小川なつみ, 加藤広海, 岸田康平, 野々山翔太, 永田裕二, 大坪嘉行, 津田雅孝

    日本ゲノム微生物学会年会要旨集   13th   2019

  • ナフタレン分解遺伝子有すプラスミドNAH7の新規接合伝達必須遺伝子の同定

    岸田康平, 野々山翔太, 永田裕二, 大坪嘉行, 津田雅孝

    日本農芸化学会東北支部大会プログラム・講演要旨集   153rd   2018

  • IncP-9群プラスミドNAH7の新規な接合伝達必須遺伝子の機能解明

    岸田康平, LUCAS Tim, 野々山翔太, 永田裕二, 大坪嘉行, 津田雅孝

    日本農芸化学会大会講演要旨集(Web)   2018   2018

  • ナフタレン分解プラスミドNAH7の接合伝達に必須な遺伝子セットの同定

    岸田康平, LUCAS Tim, 野々山翔太, 永田裕二, 大坪嘉行, 津田雅孝

    日本ゲノム微生物学会年会要旨集   12th   2018

  • Burkholderia multivoransの鉄硫黄クラスター生合成遺伝子群に対する転写因子Fur及びIscRの作用機序

    野々山翔太, 佐藤拓哉, 岸田康平, 大坪嘉行, 永田裕二, 津田雅孝

    日本ゲノム微生物学会年会要旨集   11th   2017

  • 土壌細菌Burkholderia multivoransにおける鉄硫黄クラスター生合成系の転写制御機構の解析

    野々山翔太, 佐藤拓哉, 岸田康平, 大坪嘉行, 永田裕二, 津田雅孝

    日本農芸化学会大会講演要旨集(Web)   2017   2017

  • Burkholderia multivoransにおける鉄硫黄クラスター合成遺伝子群の転写制御に対するFur及びIscRの作用機作

    野々山翔太, 佐藤拓哉, 岸田康平, 大坪嘉行, 永田裕二, 津田雅孝

    日本ゲノム微生物学会年会要旨集   10th   2016

  • Burkholderia multivoransにおける鉄硫黄クラスター合成系遺伝子群の転写制御機構の解析

    野々山翔太, 佐藤拓哉, 岸田康平, 大坪嘉行, 永田裕二, 津田雅孝

    日本農芸化学会大会講演要旨集(Web)   2016   2016

▼display all

Presentations

  • Mechanism of intracellular H2S-dependent activation of iron uptake in Escherichia coli Invited

    Shouta Nonoyama, Shinji Masuda

    2026.3 

     More details

    Event date: 2026.3

    Presentation type:Symposium, workshop panel (nominated)  

    researchmap

  • The H2S-responsive transcriptional regulator YgaV regulates iron uptake in response to intracellular H2S.

    Shouta NONOYAMA, Shintaro MAENO, Tetsuya HAYASHI, Shinji MASUDA

    2024.3 

     More details

    Event date: 2024.3

    researchmap

  • 硫黄化合物を介したタマネギ-Burkholderia属細菌間の相互作用のメカニズム

    野々山 翔太, 増田 真二

    第64回日本植物生理学会年会 

     More details

    Event date: 2023.3

    researchmap

  • qTn-Seq法を用いたSphingobium japonicum UT26株の超低栄養環境での増殖に関わる遺伝子の同定

    野々山 翔太, 柳 熙盟, 加藤 広海, 大坪 嘉行, 永田 裕二

    日本農芸化学会2022年度大会 

     More details

    Event date: 2022.3

    Presentation type:Oral presentation (general)  

    researchmap

  • qTnSeq 法を用いた Burkholderia 属細菌における潜在的抗生物質耐性遺伝子の網羅的同定

    野々山 翔太, 逸見 裕太郎, 永田 裕二, 大坪 嘉行

    第15回日本ゲノム微生物学会年会 

     More details

    Event date: 2021.3

    Presentation type:Poster presentation  

    researchmap

  • 土壌細菌Burkholderia multivorans における 転写制御因子IscRの解析

    野々山 翔太, 岸田 康平, 酒井 啓一郎, 永田 裕二, 津田 雅孝, 大坪 嘉行

    日本農芸化学会2021年度大会 

     More details

    Event date: 2021

    Presentation type:Oral presentation (general)  

    researchmap

  • 二機能性融合タンパク質 DahX の tRNA 編集活性

    高橋由紀子, 中鉢千尋, 野々山翔太, 佐藤優花里, 永田裕二

    日本生化学会東北支部 第 86 回例会 

     More details

    Event date: 2020.8

    Presentation type:Oral presentation (general)  

    researchmap

  • Acidovorax sp.KKS102株が有する融合酵素DahXのtRNA編集活性

    高橋由紀子, 中鉢千尋, 野々山翔太, 佐藤優花里, 永田裕二

    日本農芸化学会2020年度大会 

     More details

    Event date: 2020.3

    Presentation type:Oral presentation (general)  

    researchmap

  • Burkholderia属細菌におけるヘム獲得系活性化因子HemPの機能解析

    野々山 翔太, 岸田 康平, 永田 裕二, 大坪 嘉行, 津田 雅孝

    第13回 細菌学若手コロッセウム in みやぎ蔵王 

     More details

    Event date: 2019.8

    Presentation type:Poster presentation  

    researchmap

  • IscR of Burkholderia multivorans plays both repressing and activating roles in transcription of isc operon for biosynthesis of Fe-S cluster

    Shouta Nonoyama, KouheiKishida, Yoshiyuki Ohtsubo, Yuji Nagata, Masataka Tsuda

    8th Congress of European Microbiologists  2019.7 

     More details

    Event date: 2019.7

    Language:English   Presentation type:Poster presentation  

    researchmap

  • Mycobacterium sp. EPa45株におけるフェナントレン分解遺伝子群の転写解析

    市橋 永吉, 小川 なつみ, 加藤 広海, 岸田 康平, 野々山 翔太, 永田 裕二, 大坪 嘉行, 津田 雅孝

    第13回日本ゲノム微生物学会年会 

     More details

    Event date: 2019.3

    Presentation type:Poster presentation  

    researchmap

  • Burkholderia multivoransの鉄硫黄クラスター生合成遺伝子群における転写制御因子IscRの解析

    野々山 翔太, 永田 裕二, 大坪 嘉行, 津田 雅孝

    日本農芸化学会2018年度大会 

     More details

    Event date: 2018.3

    Presentation type:Oral presentation (general)  

    researchmap

  • Furで制御されるBurkholderia属細菌ヘム獲得系活性化因子HemPの解析

    野々山 翔太, 佐藤 拓哉, 大坪 嘉行, 永田 裕二, 津田 雅孝

    第12回日本ゲノム微生物学会年会 

     More details

    Event date: 2018.3

    Presentation type:Poster presentation  

    researchmap

  • IncP-9群プラスミドNAH7の新規な接合伝達必須遺伝子の機能解明

    岸田 康平, Tim Lucas, 野々山 翔太, 永田 裕二, 大坪 嘉行, 津田 雅孝

    日本農芸化学会2018年度大会 

     More details

    Event date: 2018.3

    Presentation type:Oral presentation (general)  

    researchmap

  • 出芽酵母におけるホウ酸耐性機構の解明

    岡田健太, 野々山翔太, 澤崎達也, 野澤彰

    第 39 回日本分子生物学会年会 

     More details

    Event date: 2016.11

    Presentation type:Poster presentation  

    researchmap

  • Identification and Characterization of A Novel Gene Essential for Conjugative Transfer of Naphthalene-Catabolic Plasmid NAH7.

    岸田 康平, 野々山 翔太, 大坪 嘉行, 永田 裕二, 津田 雅孝

    Plasmid biology 2018 Seattle, US  2018 

     More details

    Presentation type:Oral presentation (general)  

    researchmap

▼display all

Research Projects

  • 硫黄化合物を介したBurkholderia属細菌-タマネギ間相互作用メカニズムの解明

    Grant number:25K18158  2025.4 - 2028.3

    日本学術振興会  科学研究費助成事業  若手研究

    野々山 翔太

      More details

    Grant amount:\4810000 ( Direct Cost: \3700000 、 Indirect Cost:\1110000 )

    researchmap