• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[烟酰胺腺嘌呤二核苷酸激酶基因过表达对酿酒酵母乙醇发酵的影响]

[Effects of overexpression of NADH kinase gene on ethanol fermentation by Saccharomyces cerevisiae].

作者信息

Wang Han, Zhang Liang, Shi Guiyang

出版信息

Sheng Wu Gong Cheng Xue Bao. 2014 Sep;30(9):1381-9.

PMID:25720153
Abstract

Glycerol is the main byproduct in ethanol production by Saccharomyces cerevisiae. In order to improve ethanol yield and the substrate conversion, a cassette about 4.5 kb for gene homologous recombination, gpd2Δ::PGK1(PT)-POS5-HyBR, was constructed and transformed into the haploid strain S. cerevisiae S1 (MATa) to replace the GPD2 gene by POS5 gene. The NADH kinase gene POS5 was successfully over expressed in the recombinant strain S. cerevisiae S3. Comparing with the parent strain, the recombinant strain S. cerevisiae S3 exhibited an 8% increase in ethanol production and a 33.64% decrease in glycerol production in the conical flask fermentation with an initiatory glucose concentration of 150 g/L. Overexpression of NADH kinase gene seems effective in reducing glycerol production and increasing ethanol yield.

摘要

甘油是酿酒酵母生产乙醇过程中的主要副产物。为了提高乙醇产量和底物转化率,构建了一个约4.5 kb的用于基因同源重组的盒式结构gpd2Δ::PGK1(PT)-POS5-HyBR,并将其转化到单倍体酿酒酵母菌株S1(MATa)中,用POS5基因替换GPD2基因。NADH激酶基因POS5在重组菌株酿酒酵母S3中成功过表达。与亲本菌株相比,在初始葡萄糖浓度为150 g/L的锥形瓶发酵中,重组菌株酿酒酵母S3的乙醇产量提高了8%,甘油产量降低了33.64%。NADH激酶基因的过表达似乎在降低甘油产量和提高乙醇产量方面是有效的。

相似文献

1
[Effects of overexpression of NADH kinase gene on ethanol fermentation by Saccharomyces cerevisiae].[烟酰胺腺嘌呤二核苷酸激酶基因过表达对酿酒酵母乙醇发酵的影响]
Sheng Wu Gong Cheng Xue Bao. 2014 Sep;30(9):1381-9.
2
Overexpression of ZWF1 and POS5 improves carotenoid biosynthesis in recombinant Saccharomyces cerevisiae.ZWF1和POS5的过表达改善了重组酿酒酵母中的类胡萝卜素生物合成。
Lett Appl Microbiol. 2015 Oct;61(4):354-60. doi: 10.1111/lam.12463. Epub 2015 Aug 13.
3
Redox Engineering by Ectopic Overexpression of NADH Kinase in Recombinant Pichia pastoris (): Impact on Cell Physiology and Recombinant Production of Secreted Proteins.过表达 NADH 激酶对重组毕赤酵母()细胞生理和分泌蛋白重组表达的影响:氧化还原工程。
Appl Environ Microbiol. 2020 Mar 2;86(6). doi: 10.1128/AEM.02038-19.
4
Effect of NADH kinase on poly-3-hydroxybutyrate production by recombinant Escherichia coli.NADH激酶对重组大肠杆菌生产聚3-羟基丁酸酯的影响。
J Biosci Bioeng. 2016 Dec;122(6):685-688. doi: 10.1016/j.jbiosc.2016.06.005. Epub 2016 Jun 25.
5
Interruption of glycerol pathway in industrial alcoholic yeasts to improve the ethanol production.中断工业酒精酵母中的甘油途径以提高乙醇产量。
Appl Microbiol Biotechnol. 2009 Feb;82(2):287-92. doi: 10.1007/s00253-008-1777-7. Epub 2008 Nov 19.
6
[Construction of high sulphite-producing industrial strain of Saccharomyces cerevisiae].[酿酒酵母高亚硫酸盐产生工业菌株的构建]
Wei Sheng Wu Xue Bao. 2006 Feb;46(1):38-42.
7
[Improvement of inhibitors tolerance of Saccharomyces cerevisiae by overexpressing of long chain sphingoid kinases encoding gene LCB4].[通过过表达编码长链鞘氨醇激酶的基因LCB4提高酿酒酵母对抑制剂的耐受性]
Sheng Wu Gong Cheng Xue Bao. 2018 Jun 25;34(6):906-915. doi: 10.13345/j.cjb.170476.
8
Enhanced xylose fermentation by engineered yeast expressing NADH oxidase through high cell density inoculums.通过高细胞密度接种物表达NADH氧化酶的工程酵母增强木糖发酵。
J Ind Microbiol Biotechnol. 2017 Mar;44(3):387-395. doi: 10.1007/s10295-016-1899-3. Epub 2017 Jan 9.
9
Overexpression of NADH-dependent fumarate reductase improves D-xylose fermentation in recombinant Saccharomyces cerevisiae.NADH 依赖性延胡索酸还原酶过表达提高重组酿酒酵母对 D-木糖的发酵。
J Ind Microbiol Biotechnol. 2013 Dec;40(12):1383-92. doi: 10.1007/s10295-013-1344-9. Epub 2013 Oct 10.
10
Effects of NADH-preferring xylose reductase expression on ethanol production from xylose in xylose-metabolizing recombinant Saccharomyces cerevisiae.NADH 偏好木糖还原酶表达对木糖代谢重组酿酒酵母从木糖生产乙醇的影响。
J Biotechnol. 2012 Apr 30;158(4):184-91. doi: 10.1016/j.jbiotec.2011.06.005. Epub 2011 Jun 15.