研究者業績

浅水 俊平

アサミズ シュンペイ  (Shumpei Asamizu)

基本情報

所属
学習院大学 理学部 生命科学科 助教
学位
博士(工学)(2010年3月 富山県立大学)

研究者番号
90709057
ORCID ID
 https://orcid.org/0000-0002-7178-5410
J-GLOBAL ID
201701009522124891
researchmap会員ID
B000277339

論文

 63
  • Shinta Ijichi, Shumpei Asamizu, Shotaro Hoshino, Hiroyasu Onaka
    The Journal of Antibiotics 2026年10月26日  査読有り招待有り責任著者
  • Manami Takama, Takatoshi Suematsu, Takayuki Okano, Itsuki Tomita, Kenya Tanaka, Takahiro Bamba, Shumpei Asamizu, Tomohisa Hasunuma
    ACS Synthetic Biology 2026年10月24日  査読有り
    Abstract Efficient screening of high-producing strains from large combinatorial libraries remains an important challenge in synthetic biology. Hyperspectral imaging (HSI) enables the non-destructive evaluation of microbial colonies through the simultaneous acquisition of spectral and spatial information. In this study, we developed a novel screening strategy based on the clustering analysis of HSI-derived spectral data without the need to construct training strain sets with different production levels. As a proof of concept, we evaluated this approach using Escherichia coli with differential expression of biosynthetic genes for the production of a type II polyketide secondary metabolite, 1,3,8-trihydroxyanthraquinone (AQ256). A combinatorial library was constructed in which the transcription of AQ256 biosynthetic genes (antA-I and Pl-mcat) from Photorhabdus laumondii TTO1 was controlled by the T7 promoter or its variants. Clustering analysis revealed that AQ256 accumulation was divided into statistically distinct clusters, including those enriched in high-producing strains. The highest AQ256-producing strain, AQ-6′, identified through this screening, produced 49.0 mg L−1 in LB medium, which increased to 89.2 mg L−1 after optimizing cultivation conditions. Furthermore, proteomic analysis indicated that the increased expression of AntD/AntE, responsible for polyketide chain elongation, was associated with enhanced production. These results demonstrate that clustering based on HSI-derived spectral data enables the screening of high-producing strains without the need to prepare training data labeled according to production levels in advance and provides a useful strategy for enhancing type-II polyketide synthase-derived metabolite production.
  • Shingo Kobayashi, Yohei Katsuyama, Misato Matsui, Rina Aoki, Riku Matsumoto, Shumpei Asamizu, Kenya Tanaka, Takahiro Bamba, Kanji Ohshima, Tomohisa Hasunuma, Yasuo Ohnishi
    Metabolic Engineering 102574-102574 2026年10月  査読有り
  • Takatoshi Suematsu, Shumpei Asamizu, Manami Takama, Takahiro Bamba, Mami Matsuda, Itsuki Tomita, Misato Eguchi, Shumpei Hitosugi, Kenya Tanaka, Tomohisa Hasunuma
    Metabolic engineering 102557-102557 2026年9月25日  査読有り
    Malonyl-CoA is a major extender unit in polyketide biosynthesis; however, in Escherichia coli, it is predominantly consumed by fatty acid biosynthesis, limiting its availability for heterologous polyketide production. Here, we engineered a fatty acid biosynthesis-β-oxidation carbon-recycling pathway (FABOX pathway) that redirects fatty acid biosynthetic flux toward free fatty acid formation while reinforcing β-oxidation, thereby recycling carbon through acetyl-CoA to support malonyl-CoA-dependent polyketide biosynthesis. Application of this strategy to three malonyl-CoA-dependent polyketides, 1,3,8-trihydroxyanthraquinone (AQ256), phloroglucinol, and flaviolin, increased AQ256 and phloroglucinol production, whereas no clear improvement was observed for flaviolin. 13C-malonate tracing was consistent with β-oxidation-associated recycling of malonate-derived carbon into acetyl-CoA and extensive incorporation of malonate-derived carbon into AQ256. Here, we show that, although its effectiveness depends on the product and cultivation conditions, the FABOX pathway provides a mechanistically distinct flux-reconfiguration strategy for enhancing malonyl-CoA-dependent polyketide biosynthesis, complementing conventional precursor-supply-based approaches.
  • Ryotaro Yoshizumi, Shunichi Miura, Hiroaki Matoba, Go Hirai, Shumpei Asamizu, Hiroyasu Onaka, Yoko Yashiroda, Akihisa Matsuyama, Minoru Yoshida, Shinichi Nishimura
    mSystems e0012326 2026年9月14日  査読有り
    UNLABELLED: Microorganisms in nature form communities through diverse interactions, such as mutualism and competition, to adapt to their ecological environments. These interactions seem to be mediated by extracellular metabolites (exometabolites), yet the chemical and biological diversity underlying these processes remains largely unexplored. In this study, we examined the chemical basis of exometabolite-mediated interactions in the fission yeast Schizosaccharomyces pombe by a genome-wide screen employing 3,420 viable gene deletion mutants. We identified 37 strains that exhibited growth defects in monoculture on a minimal medium but exhibited growth recovery in the vicinity of wild-type colonies (co-culture), suggesting that exometabolites derived from wild-type cells compensated for the gene deletion. Both lipophilic and water-soluble fractions obtained by solvent partitioning of the wild-type culture supernatant promoted growth recovery. Among the 11 mutants rescued by the water-soluble fraction, 6 were cysteine auxotrophs, prompting analyses of thiol-containing metabolites by liquid chromatography-mass spectrometry (LC-MS), revealing the presence of glutathione (GSH) in the culture supernatant. GSH restored growth in most strains as a nutrient source. In contrast, GSH rescued cell morphology defects in the hob3∆ mutant, lacking the Bin/amphiphysin/Rvs (BAR) adaptor protein Hob3, through a mechanism independent of nutrition. This research advances understanding of exometabolite-mediated interactions in S. pombe by identifying GSH as an exometabolite that influences cellular processes and potentially shapes microbial communities. IMPORTANCE: Microorganisms secrete a wide range of metabolites that control microbial community behavior. These extracellular metabolites (exometabolites) include not only well-studied signaling molecules but also diverse primary and secondary metabolites, suggesting complex interactions among microbes. However, the molecular basis of these interactions remains poorly understood, partly due to challenges in detecting them experimentally. In this study, we surveyed exometabolites involved in cell-cell interactions in the model eukaryotic microorganism Schizosaccharomyces pombe. S. pombe releases a wide variety of metabolites outside the cells, including previously reported nitrogen signaling factors (NSFs) and glutathione (GSH) identified in this work. By analyzing gene deletion mutants whose growth is supported by extracellular GSH, we provide new insights into how secreted primary exometabolites compensate for specific genetic defects and influence cell physiology in microbial populations.
  • Fumihiro Ishikawa, Hiroyuki Izuno, Shinya Nakamura, Ryotaro Wakano, Shinta Ijichi, Shumpei Asamizu, Nao Miyazaki, Saaya Kusuhara, Hiroyasu Onaka, Isao Nakanishi, Genzoh Tanabe
    ACS chemical biology 2026年9月7日  査読有り
    Nonribosomal peptide synthetases (NRPSs) are modular assembly-line enzymes that generate structurally diverse and biologically active natural products. Although adenylation (A) domain selectivity has been extensively characterized and engineered, the specificity of condensation (C) domains, which catalyze peptide bond formation and can constrain NRPS reprogramming, remains less well understood. Here, we report a systematic functional analysis of VibH, a stand-alone C domain VibH from the vibriobactin biosynthetic pathway. By integrating VibH with wild-type and engineered variants of the upstream aryl acid A domain EntE, we bypassed intrinsic A-domain constraints and independently interrogated donor- and acceptor-site substrate tolerance. The donor site of VibH exhibited stringent specificity, accepting only mono- and disubstituted benzoic acid derivatives closely resembling 2,3-dihydroxybenzoic acid (DHB), whereas bulkier aryl substrates were not processed. In contrast, the acceptor site displayed broad tolerance toward structurally diverse amines. Monoamines showed clear chain-length dependence, with productive turnover restricted to medium-chain substrates, whereas diamines were more broadly accepted. Systematic analysis further revealed distance-dependent steric tolerance, in which bulky substituents were accommodated when positioned distal to the reactive amine but were restricted beyond an upper steric threshold. This engineered reconstitution strategy enabled the synthesis of numerous non-native amide conjugates and uncovered an asymmetric substrate-recognition architecture characterized by a stringent donor site and a permissive yet spatially constrained acceptor site. Molecular docking analysis provided a structural rationale for these trends by suggesting distinct binding modes for native and non-native donor substrates and distance-dependent accommodation of bulky amine acceptors. These findings provide mechanistic insights into C-domain specificity and establish a framework for rational NRPS reprogramming.
  • Shotaro Hoshino, Emiko Nagai, Hisayuki Komaki, Shinta Ijichi, Shumpei Asamizu, Hiroyasu Onaka
    The Journal of Antibiotics 2026年7月24日  査読有り
  • Shinta Ijichi, Shotaro Hoshino, Emiko Nagai, Shumpei Asamizu, Hiroyasu Onaka
    ACS Synthetic Biology 2026年7月3日  査読有り
  • Toshiki Nagakubo, Tatsuya Nishiyama, Shumpei Asamizu, Hiroyasu Onaka, Nobuhiko Nomura, Masanori Toyofuku
    Journal of bacteriology e0053225 2026年5月6日  査読有り
    Contractile injection systems (CISs) are derivatives of phage tails and are widely distributed in prokaryotes. CISs load cognate effectors and eject them through contractile actions resembling those of phage tails. Ejected effectors play central roles in CIS functionality by acting on target cells and mediating various biological processes. Here, we report a novel group of CIS effectors related to phage tape measure protein, the transmembrane component of the phage infection machinery. This group is broadly distributed within the class Actinobacteria, one of the bacterial classes in which CIS gene clusters are highly conserved, and is represented by Sle1, a cognate effector of the intracellularly localized Streptomyces lividans phage tail-like nanoparticle (SLP). This effector is associated with Sle2, which contains a CIS effector core domain and interacts with the SLP core component. Sle1 is packaged inside SLP and is translocated to lipid membranes along with SLPs. The functional domain of Sle1 enriches the membrane-associated subproteome in S. lividans and E. coli. This effect modifies the physiological properties of S. lividans, ultimately enhancing its adaptation to microbial competition. In addition, we revealed that Sle1-type effectors conserved among actinobacterial species are structurally and functionally diverse in their functional domains. One of them from Micromonospora eburnea constitutes a novel toxin-antitoxin system, and introducing its functional domain into Sle1 reprograms the phenotypic responsiveness of S. lividans to neighboring bacteria. Our findings illustrate that phage elements can be incorporated into CISs as reconfigurable platforms for bacterial adaptation to various environmental conditions.IMPORTANCEBacterial CISs have attracted interest for their importance in microbial ecology and potential in biotechnological applications. However, understanding of their functional diversity is currently limited because many CIS effectors remain unannotated due to a lack of inferable structural and genetic signatures. Our findings on Sle1 and its relatives illuminate a previously unidentified class of CIS effectors with phage tape measure protein-related modular architecture, association with the CIS effector core domain, and wide distribution within the major class of Actinobacteria, substantially expanding the known repertoire of effector classes. The impact of Sle1 on S. lividans suggests a link between CIS effectors and bacterial adaptation to environmental conditions, highlighting unexplored functional diversity of CIS effectors as tuners of bacterial phenotypes in communities.
  • Akiko Shimizu-Ibuka, Yoshiki Kato, Shumpei Asamizu, Hiroyasu Onaka
    Journal of molecular biology 169619-169619 2025年12月30日  査読有り
    Goadsporin is one of linear azole-containing peptides (LAPs) that form a subgroup within ribosomally synthesized and post-translationally modified peptides (RiPPs). It contains two dehydroalanine residues formed through the action of two enzymes, GodF and GodG, in a two-step process involving serine O-glutamylation followed by elimination. Here, we report the X-ray crystal structure of GodF, which catalyzes the tRNA-dependent glutamylation of target serine residues, resolved at a 2.34-Å resolution. Although GodF exhibits low homology at the primary sequence level, its overall structure closely resembles that of TbtB, a tRNAGlu-dependent enzyme involved in thiopeptide biosynthesis, as well as the O-glutamylation domains of NisB and MibB, which serve as dehydroalanine synthases in lanthipeptide biosynthesis. The residues and structural elements forming the active site are well-aligned among these enzymes, while regions outside the active site are poorly conserved. Like TbtB, GodF features a coiled-coil subdomain at its N-terminus, and AlphaFold3 predicts this region plays a key role in recognizing the substrate tRNAGlu. GodF also contains a typical RiPP recognition element (RRE) motif; however, the spatial arrangement of the secondary structural elements comprising this motif differs notably from those in other O-glutamylating enzymes. These structural characteristics of GodF highlight the diversity of substrate-binding pockets among RiPP-modifying enzymes, reflecting the variability in their substrate peptides and the necessity to accommodate distinct conformational and physicochemical properties.
  • Manami Takama, Takatoshi Suematsu, Takayuki Okano, Shumpei Asamizu, Takahiro Bamba, Tomohisa Hasunuma
    Journal of Bioscience and Bioengineering 2025年10月  査読有り
  • Takatoshi Suematsu, Manami Takama, Itsuki Tomita, Shumpei Asamizu, Takahiro Bamba, Tomohisa Hasunuma
    ACS Synthetic Biology 2025年9月16日  査読有り
  • Shumpei Asamizu
    Natural product reports 2025年7月16日  査読有り招待有り責任著者
    Covering: This review summarizes recent advances in the discovery, biosynthesis, and bioactivity of RiPP-derived lipopeptides, covering studies published up to 2024.Ribosomally synthesized and post-translationally modified peptides (RiPPs) are a diverse superfamily of natural products unified by a common biosynthetic logic: The peptide backbone is genetically encoded, and the translated precursor peptide undergoes a series of post-translational modifications catalyzed by maturase enzymes to produce the final bioactive compound. Despite their structural complexity, RiPPs are encoded by relatively small biosynthesis gene clusters. RiPP maturase enzymes are diverse and often promiscuous, offering significant biotechnological potential. However, their lack of conserved features makes genome-based discovery of novel RiPPs challenging. Recent advances in biosynthetic understanding and genome mining techniques have led to the identification of numerous uncharacterized RiPP biosynthetic gene clusters, often flanked by genes encoding non-RiPP moieties, in microbial genomes. Leveraging this information, a new class of natural products, hybrids of RiPPs and non-RiPP elements, has recently been discovered. Among them, RiPPs bearing fatty acyl groups, referred to as RiPP-derived lipopeptides, represent a newly emerging class of lipopeptide natural products with significant antimicrobial activity.
  • Sung-Jin Kawai, Shumpei Asamizu, Hiroaki Suzuki, Hiroyasu Onaka, Yoshichika Arakawa, Kouji Kimura, Makoto Ojika
    The Journal of antibiotics 2025年7月9日  査読有り筆頭著者責任著者
    Bacterial interactions can affect the production of secondary metabolites and, therefore, provide a promising approach to exploring new microbial compounds. In this study, we screened actinomycetes isolated from Hegura Island, Ishikawa Prefecture, Japan, to discover new antibiotics through combined-culture with Tsukamurella pulmonis TP-B0596. Three new phenazine-class antibiotics, griseoluteins T (1), C (2), and D (3), along with two known related metabolites, griseoluteic acid (4) and griseolutein A (5), were detected in both mono- and combined-cultures of Streptomyces seoulensis HEK131 with T. pulmonis at different production levels. Detailed spectroscopic analysis revealed that 1 contained a dihydrophenazine core, and was converted to 5 by accepting oxidation spontaneously. 1, containing a dihydrophenazine group, was relatively unstable under oxidative conditions, and the addition of ascorbate was required during the isolation of the compound. 2 and 3 were found to be cysteine-adducts analogous to 4, and their productivity was increased in the combined-culture. We further assessed the antibacterial activities of 1 against clinically significant Gram-positive pathogenic bacteria, including 30 methicillin-resistant Staphylococcus aureus (MRSA), 27 vancomycin-resistant Enterococci (VRE), and 17 Clostridioides difficile. Notably, 1 was found to possess higher antibacterial activity against these microorganisms than several clinically important antibiotics, while displaying lower cytotoxicity against HeLa-S3 cells.
  • Shumpei Asamizu
    World journal of microbiology & biotechnology 41(7) 217-217 2025年6月25日  査読有り招待有り責任著者
    Bacteria form consortia as integral components of diverse ecosystems, where they interact with various organisms. Within these communities, bacterial-bacterial communication plays a pivotal role by driving numerous specific interactions. A key aspect of this chemical communication is the production of secondary metabolites. Recent research demonstrates that interspecies interactions between microorganisms can serve as physiological triggers, activating silent biosynthetic gene clusters and leading to the synthesis of novel secondary metabolites by the interacting species. This review focuses on mixed cultivation strategies involving actinobacteria, with an emphasis on utilizing mycolic acid-containing bacteria such as Tsukamurella pulmonis as inducer organisms. It comprehensively examines recent advances striving to understand these bacterial interactions, specifically involving the ability of actinomycetes to recognize and respond to mycolic acid-containing bacteria to activate secondary metabolism. Furthermore, the genetic basis of secondary metabolism activation was explored and newly discovered secondary metabolites induced by actinobacteria-mycolic acid-containing bacteria co-culture were highlighted. Finally, the integration of combined-culture strategies with genetic engineering methods and the ecological relevance of actinobacteria-mycolic acid-containing bacteria interactions were discussed. These bacterial interactions provide an excellent model system for understanding the molecular mechanisms regulating secondary metabolism and could open new avenues for drug discovery.
  • Kimberly S. Taylor, Madison M. McMonagle, Schaelee C. Guy, Ariana M. Human-McKinnon, Shumpei Asamizu, Heidi J. Fletcher, Bradley W. Davis, Takashi L. Suyama
    Organic & Biomolecular Chemistry 22(15) 2992-3000 2024年4月17日  査読有り
  • Yukun Lei, Hiroyasu Onaka, Shumpei Asamizu
    Frontiers in microbiology 15 1422977-1422977 2024年  査読有り責任著者
    Combined-cultures involving mycolic acid-containing bacteria (MACB) can stimulate secondary metabolite (SM) production in actinomycetes. In a prior investigation, we screened Streptomyces coelicolor JCM4020 mutants with diminished production of SMs, specifically undecylprodigiosin (RED), which was enhanced by introducing the MACB Tsukamurella pulmonis TP-B0596. In this study, we conducted mutational analysis that pinpointed the sco1842 gene, which we assigned the gene name ccr1 (combined-culture related regulatory protein no. 1), as a crucial factor in the deficient phenotype observed in the production of various major SMs in S. coelicolor A3(2). Notably, the Ccr1 (SCO1842) homolog was found to be highly conserved throughout the Streptomyces genome. Although Ccr1 lacked conserved motifs, in-depth examination revealed the presence of a helix-turn-helix (HTH) motif in the N-terminal region and a helicase C-terminal domain (HCTD) motif in the C-terminal region in some of its homologs. Ccr1 was predicted to be a nucleoid-associated protein (NAP), and its impact on gene transcription was validated by RNA-seq analysis that revealed genome-wide variations. Furthermore, RT-qPCR demonstrated that ccr1 was transcriptionally activated in combined-culture with T. pulmonis, which indicated that Ccr1 is involved in the response to bacterial interaction. We then investigated Streptomyces nigrescens HEK616 in combined-culture, and the knockout mutant of the ccr1 homolog displayed reduced production of streptoaminals and 5aTHQs. This finding reveals that the Ccr1 homolog in Streptomyces species is associated with SM production. Our study elucidates the existence of a new family of NAP-like proteins that evolved in Streptomyces species and play a pivotal role in SM production.
  • Shotaro Hoshino, Shinta Ijichi, Shumpei Asamizu, Hiroyasu Onaka
    Journal of the American Chemical Society 145(32) 17863-17871 2023年8月16日  査読有り
  • Fumihiro Ishikawa, Natsumi Tsukumo, Erika Morishita, Shumpei Asamizu, Saaya Kusuhara, Shinsuke Marumoto, Katsuki Takashima, Hiroyasu Onaka, Genzoh Tanabe
    Chemical Communications 59(62) 9473-9476 2023年8月1日  査読有り
  • Toshiki Nagakubo, Shumpei Asamizu, Tatsuya Yamamoto, Manami Kato, Tatsuya Nishiyama, Masanori Toyofuku, Nobuhiko Nomura, Hiroyasu Onaka
    mSphere 8(3) e0011423 2023年6月22日  査読有り
  • Shinta Ijichi, Shotaro Hoshino, Shumpei Asamizu, Hiroyasu Onaka
    Bioorganic & Medicinal Chemistry Letters 89 129323 2023年6月1日  査読有り責任著者
  • Yukun Lei, Shumpei Asamizu, Takumi Ishizuka, Hiroyasu Onaka
    Applied and Environmental Microbiology 89(3) e0182222 2023年5月9日  査読有り責任著者
  • Takeshi Tsunoda, Shumpei Asamizu, Taifo Mahmud
    Biochemistry 61(22) 2628-2635 2022年11月15日  査読有り
  • Shumpei Asamizu, Shinta Ijichi, Shotaro Hoshino, Hansaem Jo, Hidenori Takahashi, Yuko Itoh, Sohkichi Matsumoto, Hiroyasu Onaka
    ACS Chemical Biology 17(10) 2936-2944 2022年10月21日  査読有り筆頭著者責任著者
  • Shumpei Asamizu, Abrory Agus Cahya Pramana, Sung-Jin Kawai, Yoshichika Arakawa, Hiroyasu Onaka
    ACS Chemical Biology 17(9) 2664-2672 2022年9月16日  査読有り筆頭著者責任著者
  • Masaomi Yanagisawa, Shumpei Asamizu, Katsuya Satoh, Yutaka Oono, Hiroyasu Onaka
    PLoS One 17(7) e0270379 2022年7月14日  査読有り筆頭著者責任著者
  • Manami Kato, Shumpei Asamizu, Hiroyasu Onaka
    Scientific Reports 12(1) 7222 2022年5月4日  査読有り筆頭著者責任著者
  • Ayumi Hikima, Shumpei Asamizu, Hiroyasu Onaka, Huiping Zhang, Hiroshi Tomoda, Nobuhiro Koyama
    The Journal of Antibiotics 75(2) 72-76 2022年2月  査読有り
  • Yoshiki Asai, Tomoshige Hiratsuka, Miyu Ueda, Yumi Kawamura, Shumpei Asamizu, Hiroyasu Onaka, Manabu Arioka, Shinichi Nishimura, Minoru Yoshida
    ACS Chemical Biology 17(1) 207-216 2022年1月21日  査読有り
  • Toshiki Nagakubo, Tatsuya Yamamoto, Shumpei Asamizu, Masanori Toyofuku, Nobuhiko Nomura, Hiroyasu Onaka
    Scientific Reports 11(1) 20116 2021年10月11日  査読有り
  • Ryosuke Kozakai, Takuto Ono, Shotaro Hoshino, Hidenori Takahashi, Yohei Katsuyama, Yoshinori Sugai, Taro Ozaki, Kazuya Teramoto, Kanae Teramoto, Koichi Tanaka, Ikuro Abe, Shumpei Asamizu, Hiroyasu Onaka
    Nature chemistry 12(9) 869-877 2020年9月12日  査読有り
  • Alexander A Vinogradov, Morito Shimomura, Yuki Goto, Taro Ozaki, Shumpei Asamizu, Yoshinori Sugai, Hiroaki Suga, Hiroyasu Onaka
    Nature communications 11(1) 2272 2020年5月8日  査読有り
  • Lu-Min Vaario, Shumpei Asamizu, Tytti Sarjala, Norihisa Matsushita, Hiroyasu Onaka, Yan Xia, Hiroyuki Kurokochi, Shin-Ichi Morinaga, Jian Huang, Shijie Zhang, Chunlan Lian
    Symbiosis 81 1-13 2020年4月23日  査読有り
  • Ryosuke Sugiyama, Takahiro Nakatani, Shinichi Nishimura, Kei Takenaka, Taro Ozaki, Shumpei Asamizu, Hiroyasu Onaka, Hideaki Kakeya
    Angewandte Chemie (International ed. in English) 58(38) 13486-13491 2019年9月16日  査読有り
  • Taro Ozaki, Ryosuke Sugiyama, Morito Shimomura, Shinichi Nishimura, Shumpei Asamizu, Yohei Katsuyama, Hideaki Kakeya, Hiroyasu Onaka
    Organic & Biomolecular Chemistry 17(9) 2370-2378 2019年2月27日  査読有り
  • 尾仲 宏康, 丸山 潤一, 浅水 俊平, 黒岩 真弓, 北本 勝ひこ, 山田 雅人, 五島 徹也, 赤尾 健
    日本醸造協会誌 114(10) 645-653 2019年  
    富山県高岡市産大麦麦芽より醸造に適した「とやま産まれの酵母」を分離した。本菌株はITS領域解析の結果,Saccharomyces cerevsiae NBRC2114(Kotobukiya whisky No. 1)に最も近い配列を有することが明らかとなった。清酒小仕込み試験による醸造特性解析の結果,とやま産まれの酵母のもろみ日数はK701よりも3日長くなったものの,両者の到達アルコール濃度はほぼ同じ18%であった。K701と比較し,有機酸組成では酢酸,リンゴ酸,コハク酸の含有量が顕著に異なっており,揮発性物質では高級アルコール含量が高く,エステル類の含量が低かった。アミノ酸度はとやま酵母の方が顕著に高かった。これらの性質が官能特性評価にも現れており,K701に比較して,酸味の違いや,旨み,重い,雑味などの味の多さに特徴がある個性的な酒質であった。<br>とやま産まれの酵母による実地醸造は成政酒造にて,これまでに5回行われており,試行錯誤の末,現在では比較的濃醇でキレのある酒質となっている。また,本酵母は野生酵母で特定の酒類醸造に特化した育種もなされていないため,富山県地域のクラフトビール,ワイン,ウイスキーの醸造にも利用されるに至っている。
  • Shotaro Hoshino, Chin Piow Wong, Masahiro Ozeki, Huiping Zhang, Fumiaki Hayashi, Takayoshi Awakawa, Shumpei Asamizu, Hiroyasu Onaka, Ikuro Abe
    The Journal of Antibiotics 71(7) 653-657 2018年7月  査読有り
  • Shotaro Hoshino, Masahiro Okada, Takayoshi Awakawa, Shumpei Asamizu, Hiroyasu Onaka, Ikuro Abe
    Organic letters 19(18) 4992-4995 2017年9月15日  査読有り
  • Shumpei Asamizu
    Bioscience, biotechnology, and biochemistry 81(5) 871-881 2017年5月4日  査読有り招待有り責任著者
    Abstract Actinomycetes are a major source of bioactive natural products with important pharmaceutical properties. Understanding the natural enzymatic assembly of complex small molecules is important for rational metabolic pathway design to produce “artificial” natural products in bacterial cells. This review will highlight current research on the biosynthetic mechanisms of two classes of nitrogen-containing natural products, C7N aminocyclitols and bis-indoles. Validamycin A is a member of C7N aminocyclitol natural products from Streptomyces hygroscopicus. Here, two important biosynthetic steps, pseudoglycosyltranferase-catalyzed C–N bond formation, and C7-sugar phosphate cyclase-catalyzed divergent carbasugar formation, will be reviewed. In addition, the bis-indolic natural products indolocarbazole, staurosporine from Streptomyces sp. TP-A0274, and rearranged bis-indole violacein from Chromobacterium violaceum are reviewed including the oxidative course of the assembly pathway for the bis-indolic scaffold. The identified biosynthesis mechanisms will be useful to generating new biocatalytic tools and bioactive compounds.
  • Andrew R Osborn, Kelsey M Kean, Khaled M Alseud, Khaled H Almabruk, Shumpei Asamizu, Janet A Lee, P Andrew Karplus, Taifo Mahmud
    ACS Chemical Biology 12(4) 979-988 2017年4月21日  査読有り
  • Taro Ozaki, Kona Yamashita, Yuki Goto, Morito Shimomura, Shohei Hayashi, Shumpei Asamizu, Yoshinori Sugai, Haruo Ikeda, Hiroaki Suga, Hiroyasu Onaka
    Nature communications 8 14207 2017年2月6日  査読有り
  • Ryosuke Sugiyama, Shinichi Nishimura, Taro Ozaki, Shumpei Asamizu, Hiroyasu Onaka, Hideaki Kakeya
    Angewandte Chemie (International ed. in English) 55(35) 10278-10282 2016年8月22日  査読有り
  • Taro Ozaki, Yukari Kurokawa, Shohei Hayashi, Naoya Oku, Shumpei Asamizu, Yasuhiro Igarashi, Hiroyasu Onaka
    Chembiochem : a European journal of chemical biology 17(3) 218-223 2016年2月2日  査読有り
  • Shumpei Asamizu, Taro Ozaki, Kanae Teramoto, Katsuya Satoh, Hiroyasu Onaka
    PLoS One 10(11) e0142372 2015年11月6日  査読有り筆頭著者責任著者
  • Hiroyasu Onaka, Taro Ozaki, Yukiko Mori, Masumi Izawa, Shohei Hayashi, Shumpei Asamizu
    The Journal of Antibiotics 68(9) 594-597 2015年9月  査読有り
  • Andrew R Osborn, Khaled H Almabruk, Garrett Holzwarth, Shumpei Asamizu, Jane LaDu, Kelsey M Kean, P Andrew Karplus, Robert L Tanguay, Alan T Bakalinsky, Taifo Mahmud
    eLife 4 e05919 2015年5月12日  査読有り
  • Ryosuke Sugiyama, Shinichi Nishimura, Taro Ozaki, Shumpei Asamizu, Hiroyasu Onaka, Hideaki Kakeya
    Organic letters 17(8) 1918-1921 2015年4月17日  査読有り
  • Kelsey M Kean, Sara J Codding, Shumpei Asamizu, Taifo Mahmud, P Andrew Karplus
    Biochemistry 53(26) 4250-4260 2014年7月8日  査読有り
  • Shohei Hayashi, Taro Ozaki, Shumpei Asamizu, Haruo Ikeda, Satoshi Ōmura, Naoya Oku, Yasuhiro Igarashi, Hiroshi Tomoda, Hiroyasu Onaka
    Chemistry & Biology 21(5) 679-688 2014年5月22日  査読有り
  • Kentaro Haginaka, Shumpei Asamizu, Taro Ozaki, Yasuhiro Igarashi, Tamotsu Furumai, Hiroyasu Onaka
    Bioscience, Biotechnology, and Biochemistry 78(3) 394-399 2014年3月4日  査読有り

MISC

 17
  • Ryotaro Yoshizumi, Shunichi Miura, Hiroaki Matoba, Go Hirai, Shumpei Asamizu, Hiroyasu Onaka, Yoko Yashiroda, Akihisa Matsuyama, Minoru Yoshida, Shinichi Nishimura
    bioRxiv 2026年1月22日  
    Abstract Microorganisms in nature form communities through diverse interactions, such as mutualism and competition, to adapt to their ecological environments. These interactions seem to be mediated by extracellular metabolites (exometabolites), yet the chemical and biological diversity underlying these processes remains largely unexplored. In this study, we examined the chemical basis of cell-cell communication in the fission yeast Schizosaccharomyces pombe by a genome-wide screen employing 3,420 viable gene deletion mutants. We identified 37 strains that exhibited growth defects in monoculture on a minimal medium but exhibited growth recovery in the vicinity of wild-type colonies (co-culture), suggesting that exometabolites secreted by wild-type cells compensated for the gene deletion. Both lipophilic and water-soluble fractions obtained by solvent partitioning of the wild-type culture supernatant promoted growth recovery. Among the 11 mutants rescued by the water-soluble fraction, six were cysteine auxotrophs, prompting analyses of thiol-containing metabolites by liquid chromatography-mass spectrometry (LC-MS), revealing the presence of glutathione (GSH) in the culture supernatant. GSH restored growth in most strains as a nutrient source. In contrast, GSH rescued cell morphology defects in the hob3 Δ mutant, lacking the Bin/Amphiphysin/Rvs (BAR) adaptor protein Hob3, through a mechanism independent of nutrition. This research advances understanding of exometabolite-mediated interactions in S. pombe by highlighting the role of GSH as one of the communication molecules that influence cellular processes and shape microbial communities. Author summary Microorganisms secrete a wide range of metabolites that control microbial community behavior. These extracellular metabolites (exometabolites) include not only well-studied signaling molecules but also diverse primary and secondary metabolites, suggesting complex interactions among microbes. However, the molecular basis of these interactions remains poorly understood, partly due to challenges in detecting them experimentally. In this study, we surveyed exometabolites involved in cell-cell interactions in the model eukaryotic microorganism Schizosaccharomyces pombe . S. pombe secretes a wide variety of metabolites, including previously reported nitrogen signaling factors (NSFs) and glutathione identified in this work. By analyzing gene deletion mutants that depend on GSH for growth, we provide new insights into how microbes regulate collective behavior by sharing exometabolites.
  • Toshiki Nagakubo, Tatsuya Nishiyama, Shumpei Asamizu, Hiroyasu Onaka, Nobuhiko NOMURA, Masanori Toyofuku
    bioRxiv e0053225 2025年11月6日  
    Contractile injection systems (CISs) are derivatives of phage tails and widely distributed in prokaryotes. CISs load cognate effectors and eject them through contractile actions resembling those of phage tails. Ejected effectors play central roles in CIS functionality by acting on target cells and mediating various biological processes. Here, we report a novel group of CIS effectors related to phage tapemeasure protein, the transmembrane component of the phage infection machinery. This group is broadly distributed within the class actinobacteria, one of the bacterial classes in which CIS gene clusters are highly conserved, and is represented by Sle1, a cognate effector of the intracellularly localised Streptomyces lividans phage tail-like nanoparticle (SLP). This effector is associated with Sle2, which contains a CIS effector core domain and interacts with the SLP core component. Sle1 is packaged inside SLP and is translocated to lipid membranes along with SLPs. The functional domain of Sle1, probably through interactions with ribosome-containing subcellular fractions, upregulates the membrane-associated proteome in S. lividans and E. coli . This effect modifies the physiological properties of S. lividans , ultimately enhancing its adaptation to microbial competition. In addition, we revealed that Sle1-type effectors conserved among actinobacterial species are structurally and functionally diverse in their functional domains. One of them from Micromonospora eburnea constitutes a novel toxin-antitoxin system and introducing its functional domain into Sle1 reprogrammes the phenotypic responsiveness of S. lividans to neighbouring bacteria. Our findings illustrate that phage elements can be incorporated into CISs as reconfigurable platforms for bacterial adaptation to various environmental conditions.
  • Manami Kato, Shumpei Asamizu, Hiroyasu Onaka
    bioRxiv 2023年1月13日  
    Abstract Chemical cross talks between Mycolicibacterium septicum HEK138M and Bacillus subtilis 168 affect the bacterial morphology of Streptomyces variegatus HEK138A. We found that S. variegatus exhibits unusual hyphae branching by the bacterial interaction. We aimed to elucidate the mechanism by performing activity guided purification of substances that induce the unusual cell morphology. We found that pyrogallol, a redox active aromatic small molecule induced significant hyphae branching in S. variegatus and the activity was also observed in some of other Streptomyces species. Interestingly, the pyrogallol activity was diminished by adding catalase, which broke down H 2 O 2 . To further confirm the involvement, H 2 O 2 was tested and similar activity which induced hyphal branching was observed. This indicates that reactive oxygen species (ROS) generated by redox-active compound (RAC) is the inducing factor of hyphae branching. Further investigation revealed that pyrogallol was generated by NahG enzyme homolog of M. septicum using 2,3-dihydroxybenzoic acid as substrate by heterologous expression in E. coli . Moreover, co-culture with gene knock-out mutants revealed that 2,3-dihydroxybenzoic acid was supplied by B. subtilis produced as intermediate of bacterial siderophore bacillibactin. Since the hyphae branching of vegetative mycelium can increase the density of filamentous network and consequently help secure the milieu in soil, our results suggested that those filamentous soil bacteria use ROS which can be supplied from plant derived RAC as a signal. As those RAC ubiquitously exist in soil environment, the system will be beneficial for sensing the nutrient sources in addition to the generally considered defensive response to oxidative stress. Importance The characterization of interactions between three or more bacteria are lacking as these interactions are visually imperceptible in general. Our current study revealed changes of morphological behavior by the bacterial interaction. This study showed that hydrogen peroxide generated by redox-active compound derived from a breakdown product of siderophore can significantly increase the number of hyphae tip extension in filamentous bacteria. Our result implies the existence of oxidative response system using a low amount of reactive oxygen species as an integrated signal to sense the plant-derived carbon source by the filamentous soil bacteria. As a result of sensing, filamentous soil bacteria may decide whether the hypha tip should be extended to further explore the area or increase the tips to densify filamentous network to monopolize the nutrients in the milieu.
  • 浅水俊平
    Institute for Fermentation, Osaka. Research Communications (34) 2020年12月  
  • 尾仲宏康, 浅水俊平
    Journal of Environmental Biotechnology (Web) 20(1) 2020年6月15日  

講演・口頭発表等

 111

所属学協会

 2

共同研究・競争的資金等の研究課題

 10

産業財産権

 4