๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Heterologous expression in Bacillus subtilis II. In vitro removal of the attenuator sequence of the Escherichia coli his operon allows expression of the cloned hisG gene in B. subtilis

โœ Scribed by Buvoli, M.; Damiani, G.; Ferretti, L.; Testori, A.; Sgaramella, V.

Book ID
122866945
Publisher
Elsevier Science
Year
1986
Tongue
English
Weight
954 KB
Volume
47
Category
Article
ISSN
0378-1119

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Expression of the Bacillus subtilis polC
Expression of the Bacillus subtilis polC gene in Escherichia coli
โœ Ott, Russell W. ;Goodman, Laurie E. ;Ganesan, A. T. ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› Springer ๐ŸŒ English โš– 798 KB

We have cloned a 14 kb DNA segment containing the coding sequence (polC) for DNA polymerase III (PolIII) from the Bacillus subtilis chromosome. The plasmid carrying the sequence, pRO10, directs the synthesis of the 160 kDa PolIII protein and three additional polypeptides in Escherichia coli maxicell

Restriction and modification in Bacillus
Restriction and modification in Bacillus subtilis: Expression of the cloned methyltransferase gene from B. subtilis phage SPR in E. coli and B. subtilis
โœ Montenegro, M. A. ;Pawlek, B. ;Behrens, B. ;Trautner, T. A. ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› Springer ๐ŸŒ English โš– 451 KB

Expression of the SPR methyltransferase gene from B. subtilis phage SPR cloned into lambda and SPP1 was studied by analyzing the sensitivity of the hybrid phage DNAs to restriction by the enzymes HaeIII, MspI, and HpaII. The following results were obtained: (1) The genes were expressed both in the h

Modification of central metabolic pathwa
Modification of central metabolic pathway in escherichia coli to reduce acetate accumulation by heterologous expression of the bacillus subtilis acetolactate synthase gene
โœ Aristos A. Aristidou; Ka-Yiu San; George N. Bennett ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 736 KB

## Abstract A novel metabolic engineering technique involving the redirection ofcellular carbon fluxes was employed to reduce acetate production in an __Escherichia coli__ culture. Metabolic engineering was achieved by cloning __E. coli__ the gene for the __Bacillus subtilis__ acetolactate synthase