Suppr超能文献

通过基因改造大肠杆菌以增强从废水中生物去除磷酸盐的能力。

Genetic improvement of Escherichia coli for enhanced biological removal of phosphate from wastewater.

作者信息

Kato J, Yamada K, Muramatsu A, Ohtake H

机构信息

Department of Fermentation Technology, Hiroshima University, Japan.

出版信息

Appl Environ Microbiol. 1993 Nov;59(11):3744-9. doi: 10.1128/aem.59.11.3744-3749.1993.

Abstract

The ability of Escherichia coli MV1184 to accumulate inorganic phosphate (Pi) was enhanced by manipulating the genes involved in the transport and metabolism of Pi. The high-level Pi accumulation was achieved by modifying the genetic regulation and increasing the dosage of the E. coli genes encoding polyphosphate kinase (ppk), acetate kinase (ackA), and the phosphate-inducible transport system (pstS, pstC, pstA, and pstB). Acetate kinase was employed as an ATP regeneration system for polyphosphate synthesis. Recombinant strains, which contained either pBC29 (carrying ppk) or pEP02.2 (pst operon), removed approximately two- and threefold, respectively, more Pi from minimal medium than did the control strain. The highest rates of Pii removal were obtained by strain MV1184 containing pEP03 (ppk and ackA). However, unlike the control strain, MV1184 (pEP03) released Pi to the medium after growth had stopped. Drastic changes in growth and Pi uptake were observed when pBC29 (ppk) and pEP02.2 (pst operon) were introduced simultaneously into MV1184. Even though growth of this recombinant was severely limited in minimal medium, the recombinant could remove approximately threefold more Pi than the control strain. Consequently, the phosphorus content of this recombinant reached a maximum of approximately 16% on a dry weight basis (49% as phosphate).

摘要

通过操纵参与无机磷酸盐(Pi)转运和代谢的基因,增强了大肠杆菌MV1184积累无机磷酸盐的能力。通过改变基因调控并增加编码多聚磷酸盐激酶(ppk)、乙酸激酶(ackA)以及磷酸盐诱导转运系统(pstS、pstC、pstA和pstB)的大肠杆菌基因剂量,实现了高水平的Pi积累。乙酸激酶被用作多聚磷酸盐合成的ATP再生系统。含有pBC29(携带ppk)或pEP02.2(pst操纵子)的重组菌株从基本培养基中去除的Pi分别比对照菌株多约两倍和三倍。去除Pi的最高速率是由含有pEP03(ppk和ackA)的菌株MV1184获得的。然而,与对照菌株不同,MV1184(pEP03)在生长停止后会将Pi释放到培养基中。当将pBC29(ppk)和pEP02.2(pst操纵子)同时导入MV1184时,观察到生长和Pi摄取发生了剧烈变化。尽管该重组体在基本培养基中的生长受到严重限制,但该重组体去除的Pi比对照菌株多约三倍。因此,该重组体的磷含量以干重计最高可达约16%(以磷酸盐计为49%)。

相似文献

4
[Function of Polyphosphate Kinase Gene in Biological Phosphate Removal During the Wastewater Treatment Process].
Huan Jing Ke Xue. 2017 Apr 8;38(4):1529-1535. doi: 10.13227/j.hjkx.201606164.
6
Polyphosphate metabolism in Escherichia coli.大肠杆菌中的多聚磷酸盐代谢
Ann N Y Acad Sci. 1994 Nov 30;745:77-91. doi: 10.1111/j.1749-6632.1994.tb44365.x.
7
Molecular aspects of phosphate transport in Escherichia coli.大肠杆菌中磷酸盐转运的分子机制
Mol Microbiol. 1990 Jul;4(7):1083-90. doi: 10.1111/j.1365-2958.1990.tb00682.x.

引用本文的文献

7
Alternative promoters in the pst operon of Escherichia coli.大肠杆菌 pst 操纵子中的替代启动子。
Mol Genet Genomics. 2010 Dec;284(6):489-98. doi: 10.1007/s00438-010-0584-x. Epub 2010 Oct 21.
8
Breeding of wastewater treatment yeasts that accumulate high concentrations of phosphorus.积累高浓度磷的废水处理酵母的培育
Appl Microbiol Biotechnol. 2008 Aug;80(2):331-8. doi: 10.1007/s00253-008-1529-8. Epub 2008 Jul 5.

本文引用的文献

3
Polyphosphate metabolism in micro-organisms.微生物中的多磷酸盐代谢
Adv Microb Physiol. 1983;24:83-171. doi: 10.1016/s0065-2911(08)60385-9.
5
7
Luxury uptake of phosphate by activated sludge.
J Water Pollut Control Fed. 1973 Dec;45(12):2444-62.
9
Production of single-stranded plasmid DNA.单链质粒DNA的制备。
Methods Enzymol. 1987;153:3-11. doi: 10.1016/0076-6879(87)53044-0.

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