袁文杰

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教授

博士生导师

硕士生导师

主要任职:生物工程学院副院长

其他任职:辽宁省生物工程教指委秘书长

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:生物工程学院

学科:生物化工

办公地点:生物楼321

联系方式:0411-84706802

电子邮箱:ywj@dlut.edu.cn

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Synergistic effect of thioredoxin and its reductase from Kluyveromyces marxianus on enhanced tolerance to multiple lignocellulose-derived inhibitors

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论文类型:期刊论文

第一作者:Gao, Jiaoqi

通讯作者:Yuan, WJ (reprint author), Dalian Univ Technol, Sch Life Sci & Biotechnol, Dalian 116024, Peoples R China.

合写作者:Yuan, Wenjie,Li, Yimin,Bai, Fengwu,Jiang, Yu

发表时间:2017-10-30

发表刊物:MICROBIAL CELL FACTORIES

收录刊物:SCIE、PubMed、Scopus

卷号:16

期号:1

页面范围:181

ISSN号:1475-2859

关键字:Lignocellulose-derived inhibitors; Tolerance; Thioredoxin; Thioredoxin reductase; Ethanol fermentation; Kluyveromyces marxianus

摘要:Background: Multiple lignocellulose-derived inhibitors represent great challenges for bioethanol production from lignocellulosic materials. These inhibitors that are related to the levels of intracellular reactive oxidative species (ROS) make oxidoreductases a potential target for an enhanced tolerance in yeasts.
   Results: In this study, the thioredoxin and its reductase from Kluyveromyces marxianus Y179 was identified, which was subsequently achieved over-expression in Saccharomyces cerevisiae 280. In spite of the negative effects by expression of thioredoxin gene (KmTRX), the thioredoxin reductase (KmTrxR) helped to enhance tolerance to multiple lignocellulose-derived inhibitors, such as formic acid and acetic acid. In particular, compared with each gene expression, the double over-expression of KmTRX2 and KmTrxR achieved a better ethanol fermentative profiles under a mixture of formic acid, acetic acid, and furfural (FAF) with a shorter lag period. At last, the mechanism that improves the tolerance depended on a normal level of intracellular ROS for cell survival under stress.
   Conclusions: The synergistic effect of KmTrxR and KmTRX2 provided the potential possibility for ethanol production from lignocellulosic materials, and give a general insight into the possible toxicity mechanisms for further theoretical research.