๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The repressor of the PEP: Fructose phosphotransferase system is required for the transcription of the pps gene of Escherichia coli

โœ Scribed by Geerse, R. H. ;van der Pluijm, J. ;Postma, P. W.


Publisher
Springer
Year
1989
Tongue
English
Weight
578 KB
Volume
218
Category
Article
ISSN
0026-8925

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Cloning of the repressor protein gene of
โœ Hantke, Klaus ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Springer ๐ŸŒ English โš– 595 KB

In Escherichia coli the iron uptake systems are regulated by the fur gene product. The synthesis of the outer membrane proteins fiu, fepA, fecA, fhuA, fhuE and cir is derepressed at low iron concentrations in the medium or constitutive in a fur mutant. The fur gene region cloned into pACYC184 was an

A novel mutation FruS, altering synthesi
โœ Bolshakova, TatyanaN. ;Molchanova, MarinaL. ;Erlagaeva, RaisaS. ;Grigorenko, Yur ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Springer ๐ŸŒ English โš– 532 KB

A novel mutation, FruS localised in the fru operon was obtained. It uncouples expression of the genes determining synthesis of the fructose-specific transport proteins and fructose-1-phosphate kinase. In FruS bacteria the fruA and fruF genes (coding for Enzyme IIfru and FPr, respectively) are consti

The catabolite gene activator protein (C
โœ Ebright, Richard H. ;Beckwith, Jon ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› Springer ๐ŸŒ English โš– 519 KB

Kline et al. (1980) have reported that indole-3-acetic acid (IAA) and four other indole derivatives are able to substitute for cAMP in activating expression of the ara regulon of E. coli. We have examined this phenomenon in detail, utilizing fusions between the structural gene for beta-galactosidase

The fimD gene required for cell surface
โœ Klemm, Per ;Christiansen, Gunna ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› Springer ๐ŸŒ English โš– 645 KB

The fimD gene of Escherichia coli K12 was shown to be necessary for surface localization of type 1 fimbriae, since deletion of the gene resulted in a virtually bald phenotype. The FimD protein was found to be located in the outer membrane. Expressed alone, this protein had a very deleterious effect