• 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

利用大肠杆菌重组菌株生产L-苏氨酸过程中细菌生物质的循环利用。

Recycling of bacterial biomass in a process of L-threonine production by means of a recombinant strain of Escherichia coli.

作者信息

Blaesen Markus, Friehs Karl, Flaschel Erwin

机构信息

Bielefeld University, Faculty of Technology, Fermentation Engineering, D-33594 Bielefeld, Germany.

出版信息

J Biotechnol. 2007 Dec 1;132(4):431-7. doi: 10.1016/j.jbiotec.2007.08.011. Epub 2007 Aug 10.

DOI:10.1016/j.jbiotec.2007.08.011
PMID:17868941
Abstract

The Gram-negative bacterium Escherichia coli B-3996 represents an interesting host organism for the production of the essential amino acid L-threonine. Microbial processes - especially those of aerobic cultivation - lead to the generation of considerable amounts of biomass, thus lowering the product yield. These are the reasons for studying methods for the recycling of biomass from E. coli. It will be shown that it is possible to disintegrate the microbial biomass - preferably by means of high pressure homogenisation followed by a protease treatment of the resulting slurry of debris - in an efficient way and to recycle at least different amounts of the soluble part as cultivation medium component. By studying the growth and product formation of E. coli no adverse effects have been observed.

摘要

革兰氏阴性菌大肠杆菌B-3996是生产必需氨基酸L-苏氨酸的一种有趣的宿主生物。微生物过程——尤其是有氧培养过程——会产生大量生物质,从而降低产品产量。这些就是研究从大肠杆菌中回收生物质方法的原因。结果表明,有可能以高效的方式分解微生物生物质——最好是通过高压均质化,然后对所得碎片浆液进行蛋白酶处理——并将至少不同量的可溶部分作为培养基成分进行回收。通过研究大肠杆菌的生长和产物形成,未观察到不利影响。

相似文献

1
Recycling of bacterial biomass in a process of L-threonine production by means of a recombinant strain of Escherichia coli.利用大肠杆菌重组菌株生产L-苏氨酸过程中细菌生物质的循环利用。
J Biotechnol. 2007 Dec 1;132(4):431-7. doi: 10.1016/j.jbiotec.2007.08.011. Epub 2007 Aug 10.
2
Development of sucrose-utilizing Escherichia coli K-12 strain by cloning β-fructofuranosidases and its application for L-threonine production.通过克隆β-呋喃果糖苷酶开发利用蔗糖的大肠杆菌 K-12 菌株及其在 L-苏氨酸生产中的应用。
Appl Microbiol Biotechnol. 2010 Oct;88(4):905-13. doi: 10.1007/s00253-010-2825-7. Epub 2010 Aug 14.
3
Bacterial fermentation of recombinant major wasp allergen Antigen 5 using oxygen limiting growth conditions improves yield and quality of inclusion bodies.在限氧生长条件下利用重组黄蜂主要过敏原抗原5进行细菌发酵可提高包涵体的产量和质量。
Protein Expr Purif. 2006 Jun;47(2):621-8. doi: 10.1016/j.pep.2006.01.009. Epub 2006 Feb 8.
4
[Selection of bacterial strains for the production of threonine].[用于苏氨酸生产的细菌菌株的筛选]
Rev Argent Microbiol. 1984;16(4):209-17.
5
Culture conditions for improvement of L-threonine production using a genetically self-cloned L-threonine hyperproducing strain of Escherichia coli K-12.利用基因自克隆的大肠杆菌K-12 L-苏氨酸高产菌株提高L-苏氨酸产量的培养条件
Biosci Biotechnol Biochem. 1995 Jun;59(6):1095-8. doi: 10.1271/bbb.59.1095.
6
Improved L-threonine production of Escherichia coli mutant by optimization of culture conditions.通过优化培养条件提高大肠杆菌突变体的L-苏氨酸产量。
J Biosci Bioeng. 2006 Feb;101(2):127-30. doi: 10.1263/jbb.101.127.
7
Effects of feeding and induction strategy on the production of BmR1 antigen in recombinant E. coli.培养和诱导策略对重组大肠杆菌中BmR1抗原产生的影响。
Lett Appl Microbiol. 2009 Nov;49(5):544-50. doi: 10.1111/j.1472-765X.2009.02694.x.
8
A proposed feeding strategy for the overproduction of recombinant proteins in Escherichia coli.一种用于在大肠杆菌中过量生产重组蛋白的拟议喂养策略。
Biotechnol Appl Biochem. 2008 Feb;49(Pt 2):141-7. doi: 10.1042/BA20070089.
9
High fermentative production of L-threonine from acetate by a Brevibacterium flavum stabilized strain transformed with a recombinant plasmid carrying the Escherichia coli thr operon.用携带大肠杆菌苏氨酸操纵子的重组质粒转化的黄色短杆菌稳定菌株从乙酸盐中高效发酵生产L-苏氨酸。
Biosci Biotechnol Biochem. 1993 Oct;57(10):1755-6. doi: 10.1271/bbb.57.1755.
10
Proteome-based identification of fusion partner for high-level extracellular production of recombinant proteins in Escherichia coli.基于蛋白质组学鉴定用于在大肠杆菌中高效胞外生产重组蛋白的融合伴侣。
Biotechnol Bioeng. 2008 Oct 15;101(3):587-601. doi: 10.1002/bit.21898.