Kato J, Yamada K, Muramatsu A, Ohtake H
Department of Fermentation Technology, Hiroshima University, Japan.
Appl Environ Microbiol. 1993 Nov;59(11):3744-9. doi: 10.1128/aem.59.11.3744-3749.1993.
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).
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%)。