Altered sterol composition mediates multiple tolerance of Kluyveromyces marxianus for xylitol production.

IF 4.3 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Lili Ren, Hao Zha, Qi Zhang, Yujie Xie, Jiacheng Li, Zhongmei Hu, Xiurong Tao, Dayong Xu, Feng Li, Biao Zhang
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引用次数: 0

Abstract

Background: Currently, the synthesis of compounds based on microbial cell factories is rapidly advancing, yet it encounters several challenges. During the production process, engineered strains frequently encounter disturbances in the cultivation environment or the impact of their metabolites, such as high temperature, acid-base imbalances, hypertonicity, organic solvents, toxic byproducts, and mechanical damage. These stress factors can constrain the efficiency of microbial fermentation, resulting in slow cell growth, decreased production, significantly increased energy consumption, and other issues that severely limit the application of microbial cell factories.

Results: This study demonstrated that sterol engineering in Kluyveromyces marxianus, achieved by overexpressing or deleting the coding genes for the last five steps of ergosterol synthase (Erg2-Erg6), altered the composition and ratio of sterols in its cell membrane, and affected its multiple tolerance. The results suggest that the knockout of the Erg5 can enhance the thermotolerance of K. marxianus, while the overexpression of the Erg4 can improve its acid tolerance. Additionally, engineering strain overexpressed Erg6 improved its tolerance to elevated temperature, hypertonic, and acid. YZB453, obtained by overexpressing Erg6 in an engineering strain with high efficiency in synthesizing xylitol, produced 101.22 g/L xylitol at 45oC and 75.11 g/L xylitol at 46oC. Using corncob hydrolysate for simultaneous saccharification and fermentation (SSF) at 46oC that xylose released from corncob hydrolysate by saccharification with hemicellulase, YZB453 can produce 45.98 g/L of xylitol, saving 53.72% of the cost of hemicellulase compared to 42oC.

Conclusions: This study elucidates the mechanism by which K. marxianus acquires resistance to various antifungal drugs, high temperatures, high osmolarity, acidity, and other stressors, through alterations in the composition and ratio of membrane sterols. By employing sterol engineering, the fermentation temperature of this unconventional thermotolerant K. marxianus was further elevated, ultimately providing an efficient platform for synthesizing high-value-added xylitol from biomass via the SSF process at temperatures exceeding 45 °C.

固醇组成的改变介导了马氏克鲁维氏菌对木糖醇生产的多重耐受性。
背景:目前,基于微生物细胞工厂的化合物合成技术发展迅速,但也遇到了一些挑战。在生产过程中,工程菌株经常会遇到培养环境的干扰或其代谢产物的影响,如高温、酸碱失衡、高渗、有机溶剂、有毒副产物和机械损伤等。这些应激因素会制约微生物发酵的效率,导致细胞生长缓慢、产量下降、能耗显著增加等问题,严重限制了微生物细胞工厂的应用:本研究表明,通过过表达或删除麦角甾醇合成酶(Erg2-Erg6)最后五个步骤的编码基因,在马氏假丝酵母(Kluyveromyces marxianus)中实现了甾醇工程,改变了其细胞膜中甾醇的组成和比例,并影响了其多种耐受性。结果表明,敲除 Erg5 可提高马钱子藻的耐热性,而过表达 Erg4 则可提高其耐酸性。此外,过表达 Erg6 的工程菌株提高了对高温、高渗和酸的耐受性。在合成木糖醇效率较高的工程菌株中过表达 Erg6 后得到的 YZB453,在 45oC 时产生 101.22 克/升木糖醇,在 46oC 时产生 75.11 克/升木糖醇。利用玉米芯水解物在 46oC 温度下同时进行糖化和发酵(SSF),即利用半纤维素酶糖化玉米芯水解物释放的木糖,YZB453 可生产 45.98 克/升木糖醇,与 42oC 相比,可节省 53.72% 的半纤维素酶成本:本研究阐明了K. marxianus通过改变膜固醇的组成和比例来获得对各种抗真菌药物、高温、高渗透压、酸度和其他应激源的抗性的机制。通过采用固醇工程技术,进一步提高了这种非常规耐热 K. marxianus 的发酵温度,最终为在超过 45 °C 的温度下通过 SSF 工艺从生物质中合成高附加值木糖醇提供了一个高效平台。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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