Skip Navigation
Skip to contents

Journal of Microbiology : Journal of Microbiology

OPEN ACCESS
SEARCH
Search

Author index

Page Path
HOME > Browse Articles > Author index
Search
Jun Wu 3 Articles
Effects of tryptophan and phenylalanine on tryptophol production in Saccharomyces cerevisiae revealed by transcriptomic and metabolomic analyses
Xiaowei Gong , Huajun Luo , Liu Hong , Jun Wu , Heng Wu , Chunxia Song , Wei Zhao , Yi Han , Ya Dao , Xia Zhang , Donglai Zhu , Yiyong Luo
J. Microbiol. 2022;60(8):832-842.   Published online May 27, 2022
DOI: https://doi.org/10.1007/s12275-022-2059-2
  • 1,196 View
  • 7 Download
  • 13 Web of Science
  • 13 Crossref
AbstractAbstract PDF
Tryptophol (TOL) is a metabolic derivative of tryptophan (Trp) and shows pleiotropic effects in humans, plants and microbes. In this study, the effect of Trp and phenylalanine (Phe) on TOL production in Saccharomyces cerevisiae was determined, and a systematic interpretation of TOL accumulation was offered by transcriptomic and metabolomic analyses. Trp significantly promoted TOL production, but the output plateaued (231.02−266.31 mg/L) at Trp concentrations ≥ 0.6 g/L. In contrast, Phe reduced the stimulatory effect of Trp, which was strongly dependent on the Phe concentration. An integrated genomic, transcriptomic, and metabolomic analysis revealed that the effect of Trp and Phe on TOL production was mainly related to the transamination and decarboxylation of the Ehrlich pathway. Additionally, other genes, including thiamine regulon genes (this), the allantoin catabolic genes dal1, dal2, dal4, and the transcriptional activator gene aro80, may play important roles. These findings were partly supported by the fact that the thi4 gene was involved in TOL production, as shown by heterologous expression analysis. To the best of our knowledge, this novel biological function of thi4 in S. cerevisiae is reported here for the first time. Overall, our findings provide insights into the mechanism of TOL production, which will contribute to TOL production using metabolic engineering strategies.

Citations

Citations to this article as recorded by  
  • Modular co-culture engineering of Escherichia coli and Saccharomyces cerevisiae for de novo biosynthesis of tryptophol from glucose
    Zhenhao Fu, Jiamin Zheng, Lele Zhang, Jiansheng Jian, Zhonghu Bai, Ye Li
    Bioresource Technology.2026; 449: 134398.     CrossRef
  • An unfolded protein response-inducible protein (ULI1) mediates aromatic alcohols biosynthesis through reinforcing the Ehrlich pathway in Saccharomyces cerevisiae
    Xiaowei Gong, Yong Shen, Shanzhai Shang, Jianbo Zhan, Guanghui Ma, Huajun Luo, Shiwei Li, Chunxia Song, Donglai Zhu, Yiyong Luo
    Frontiers in Microbiology.2026;[Epub]     CrossRef
  • Recent Advances in Engineering Microbial Cell Factories for Tryptophan-Derived Chemicals
    Chenxi Qiu, Hongwei Guo, Quanpu Ren, Yujiao Sun, Ge Qu, Yongfen Wang, Ming Zheng, Zhoutong Sun
    Journal of Agricultural and Food Chemistry.2026; 74(35): 27303.     CrossRef
  • Strain-dependent modulation of selected Ehrlich pathway-associated genes during sequential fermentation with Metschnikowia pulcherrima and Saccharomyces cerevisiae
    Elif Bircan Muyanlı, Remziye Yılmaz
    European Food Research and Technology.2026;[Epub]     CrossRef
  • The effect and mechanism of acetic acid -(1H-indole-3-ethyl) ester in controlling postharvest blue mold disease in apples
    Xiangfeng Zheng, Qinghua Gong, Zhirong Wang, Peiwen Huang, Zihan Zhang, Lu Gao, Shengqi Rao, Zhenquan Yang
    Postharvest Biology and Technology.2025; 227: 113618.     CrossRef
  • Coordinated synthesis of aromatic amino acid derived pigments in yeast via global transcriptional engineering
    Huimin Xue, Mingshan Li, Yuhui Cui, Dongkui Tian, Duo Liu, Hanjie Wang
    Microbial Cell Factories.2025;[Epub]     CrossRef
  • Lysine restriction attenuates obesity-related anxiety-like behaviors via increasing Oscillibacter ruminantium-mediated tryptophol regulation
    Feng Zhao, Jiao Wang, Weijuan Liang, Fanwei Sun, Zhaoyi Liu, Yuehua Wu, Ahmad Khan, Chunsong Wang, Ruiqi Zhou, Huaili Feng, Ting You, Xinhao Duan, Hongyang Zhang, Jingfu Qiu, Chengzhi Chen
    Microbiome.2025;[Epub]     CrossRef
  • Nanostructured Biosensing Platforms for the Rapid Detection of Fungal Quorum-Sensing Molecules: Toward Early and Accurate Diagnosis of Candida albicans Infection
    Ahmed M. Saleh, Omar Ramadan, Amr M. Badawey, Hoda M. Marzouk, Shuna Cui, Rabeay Y. A. Hassan
    ACS Infectious Diseases.2025; 11(12): 3481.     CrossRef
  • Human intestinal fungus Clavispora lusitaniae attenuates colitis through Pyruvate decarboxylase-derived Indole-3-ethanol
    Fan Wu, Yan Wang, Zhenpeng Mai, Zhichao Xu, Shenghui Li, Yu Li, Ruiqiao Yin, Jiamin Li, Zhenlong Yu, Yuzhuo Wu, Xiangge Tian, Xiaoying Feng, Xiaokui Huo, Chao Wang, Xiaochi Ma
    Nature Communications.2025;[Epub]     CrossRef
  • Engineering the L-tryptophan metabolism for efficient de novo biosynthesis of tryptophol in Saccharomyces cerevisiae
    Ye Li, Jingzhen Sun, Zhenhao Fu, Yubing He, Xiaorui Chen, Shijie Wang, Lele Zhang, Jiansheng Jian, Weihua Yang, Chunli Liu, Xiuxia Liu, Yankun Yang, Zhonghu Bai
    Biotechnology for Biofuels and Bioproducts.2024;[Epub]     CrossRef
  • Evaluating the Atypical Aging Potential Development in Sparkling Wines Can Be Achieved by Assessing the Base Wines at the End of the Alcoholic Fermentation
    Simone Delaiti, Tiziana Nardin, Tomas Roman, Stefano Pedò, Roberto Larcher
    Journal of Agricultural and Food Chemistry.2024; 72(9): 4918.     CrossRef
  • Tryptophol Improves the Biocontrol Efficacy of Scheffersomyces spartinae against the Gray Mold of Strawberries by Quorum Sensing
    Zichang Zhao, Yingying Wei, Xiurong Zou, Shu Jiang, Yi Chen, Jianfen Ye, Feng Xu, Hongfei Wang, Xingfeng Shao
    Journal of Agricultural and Food Chemistry.2023; 71(49): 19739.     CrossRef
  • A comprehensive review and comparison of L-tryptophan biosynthesis in Saccharomyces cerevisiae and Escherichia coli
    Xinru Ren, Yue Wei, Honglu Zhao, Juanjuan Shao, Fanli Zeng, Zhen Wang, Li Li
    Frontiers in Bioengineering and Biotechnology.2023;[Epub]     CrossRef
Variation of cassiicolin genes among Chinese isolates of Corynespora cassiicola
Jun Wu , Xuewen Xie , Yanxia Shi , Ali Chai , Qi Wang , Baoju Li
J. Microbiol. 2018;56(9):691-691.
DOI: https://doi.org/10.1007/s12275-018-8580-7
  • 853 View
  • 0 Download
  • 2 Crossref
AbstractAbstract PDF
In the online published article by Wu et al. since 30 July 2018, the figure 4 is unfortunately incorrect. The figure 4 should be corrected as below.

Citations

Citations to this article as recorded by  
  • Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
    Shigang Gao, Rong Zeng, Lihui Xu, Zhiwei Song, Ping Gao, Fuming Dai
    BMC Microbiology.2020;[Epub]     CrossRef
  • Endophytes from Wild Rubber Trees as Antagonists of the Pathogen Corynespora cassiicola
    Valérie Pujade-Renaud, Marine Déon, Romina Gazis, Sébastien Ribeiro, Florence Dessailly, Françoise Granet, Priscila Chaverri
    Phytopathology®.2019; 109(11): 1888.     CrossRef
Variation of cassiicolin genes among Chinese isolates of Corynespora cassiicola
Jun Wu , Xuewen Xie , Yanxia Shi , Ali Chai , Qi Wang , Baoju Li
J. Microbiol. 2018;56(9):634-647.   Published online July 27, 2018
DOI: https://doi.org/10.1007/s12275-018-7497-5
  • 1,009 View
  • 2 Download
  • 12 Crossref
AbstractAbstract PDF
Corynespora cassiicola is a species of fungus that is a plant pathogen of many agricultural crop plants, including severe target spot disease on cucumber. Cassiicolin is an important effector of pathogenicity of this fungus. In this study, we collected 141 Corynespora isolates from eighteen hosts, and the casscolin gene was detected in 82 C. cassiicola strains. The deduced protein sequences revealed that 72 isolates contained the Cas2 gene, two strains from Gynura bicolor harboured the Cas2.2 gene, and 59 isolates without a cassiicolin gene were classified as Cas0. Phylogenetic analyses was performed for the 141 isolates using four loci (ITS, ga4, caa5, and act1) and revealed two genetic clusters. Cluster A is composed of four subclades: subcluster A1 includes all Cas2 isolates plus 18 Cas0 strains, subcluster A2 includes the eight Cas5 isolates and one Cas0 isolate, and subclusters A3 and A4 contain Cas0 strains. Cluster B consists of 21 Cas0 isolates. Twenty-two C. cassiicola strains from different toxin classes showed varying degrees of virulence against cucumber. Cas0 or Cas2 strains induced diverse responses on cucumber, from no symptoms to symptoms of moderate or severe infection, but all Cas5 isolates exhibited avirulence on cucumber.

Citations

Citations to this article as recorded by  
  • Diversity of cassiicolin profiles and culture filtrate toxicity of Corynespora cassiicola isolates from South Indian rubber plantations
    Reshma T R, Shilpa Babu, Vineeth V K, Shaji Philip
    Industrial Crops and Products.2025; 224: 120243.     CrossRef
  • One stop shop V: taxonomic update with molecular phylogeny for important phytopathogenic genera: 101–125 (2024)
    Ruvishika S. Jayawardena, Kevin D. Hyde, Herbert D. R. Aumentado, Pranami D. Abeywickarama, Shubhi Avasthi, Asha J. Dissanayake, Ajay K. Gautam, Achala J. Gajanayake, Alireza Armand, Mark A. O. Balendres, Mark S. Calabon, Yi Jyun Chen, K. W. Thilini Cheth
    Fungal Diversity.2025; 130(1): 263.     CrossRef
  • The Diseases and Pests of Rubber Tree and Their Natural Control Potential: A Bibliometric Analysis
    Liqiong Chen, Lidan Xu, Xiaona Li, Yilin Wang, Yun Feng, Guixiu Huang
    Agronomy.2023; 13(8): 1965.     CrossRef
  • Need for disease resistance breeding against Corynespora cassiicola in crops
    Edgar Sierra-Orozco, German Sandoya, Seonghee Lee, Gary Vallad, Samuel Hutton
    Frontiers in Agronomy.2023;[Epub]     CrossRef
  • Comparison and Correlation of Corynespora cassiicola Populations from Kiwifruit and Other Hosts Based on Morphology, Phylogeny, and Pathogenicity
    Jing Xu, Guoshu Gong, Yongliang Cui, Yuhang Zhu, Jun Wang, Kaikai Yao, Wen Chen, Cuiping Wu, Rui Yang, Xiaodan Yang, Pan Li, Henan Zhao, Sen Zhong, Yi Luo, Yue Li, Wenfei Liao
    Plant Disease.2023; 107(7): 1979.     CrossRef
  • Unraveling the Host-Selective Toxic Interaction of Cassiicolin with Lipid Membranes and Its Cytotoxicity
    Kien Xuan Ngo, Phuong Doan N. Nguyen, Hirotoshi Furusho, Makoto Miyata, Tomomi Shimonaka, Nguyen Ngoc Bao Chau, Nguyen Phuong Vinh, Nguyen Anh Nghia, Tareg Omer Mohammed, Takehiko Ichikawa, Noriyuki Kodera, Hiroki Konno, Takeshi Fukuma, Nguyen Bao Quoc
    Phytopathology®.2022; 112(7): 1524.     CrossRef
  • The necrosis- and ethylene-inducing peptide 1-like protein (NLP) gene family of the plant pathogen Corynespora cassiicola
    Thaís Carolina da Silva Dal’Sasso, Vinícius Delgado da Rocha, Hugo Vianna Silva Rody, Maximiller Dal-Bianco Lamas Costa, Luiz Orlando de Oliveira
    Current Genetics.2022; 68(5-6): 645.     CrossRef
  • Identification and virulence evaluation of Corynespora cassiicola cassiicolin-encoding gene isolates from rubber trees in Vietnam
    Nguyen Ngoc Bao Chau, Nguyen Van Minh, Nguyen Mai Nghiep, Nguyen Phuong Vinh, Nguyen Anh Nghia, Nguyen Bao Quoc
    Tropical Plant Pathology.2022; 47(3): 378.     CrossRef
  • The fungal pathogen Corynespora cassiicola: A review and insights for target spot management on cotton and Soya bean
    Marina N. Rondon, Kathy Lawrence
    Journal of Phytopathology.2021; 169(6): 329.     CrossRef
  • Mitogenome-wide comparison and phylogeny reveal group I intron dynamics and intraspecific diversification within the phytopathogen Corynespora cassiicola
    Qingzhou Ma, Haiyan Wu, Yuehua Geng, Qiang Li, Rui Zang, Yashuang Guo, Chao Xu, Meng Zhang
    Computational and Structural Biotechnology Journal.2021; 19: 5987.     CrossRef
  • Genomic Characteristics and Comparative Genomics Analysis of Two Chinese Corynespora cassiicola Strains Causing Corynespora Leaf Fall (CLF) Disease
    Boxun Li, Yang Yang, Jimiao Cai, Xianbao Liu, Tao Shi, Chaoping Li, Yipeng Chen, Pan Xu, Guixiu Huang
    Journal of Fungi.2021; 7(6): 485.     CrossRef
  • Endophytes from Wild Rubber Trees as Antagonists of the Pathogen Corynespora cassiicola
    Valérie Pujade-Renaud, Marine Déon, Romina Gazis, Sébastien Ribeiro, Florence Dessailly, Françoise Granet, Priscila Chaverri
    Phytopathology®.2019; 109(11): 1888.     CrossRef

Journal of Microbiology : Journal of Microbiology
TOP