Transcription of the argF and argI genes of the arginine biosynthetic regulon of Escherichia coli K12, performed in vitro

1977 ◽  
Vol 155 (1) ◽  
pp. 7-18 ◽  
Author(s):  
Don Sens ◽  
William Natter ◽  
Robert T. Garvin ◽  
Eric James
Keyword(s):  
Escherichia Coli ◽  
Escherichia Coli K12

Evidence for the existence of three promoters for the deo operon of Escherichia coli K12 in vitro

1979 ◽  
Vol 133 (1) ◽  
pp. 1-17 ◽  
Author(s):  
Poul Valentin-Hansen ◽  
Karin Hammer-Jespersen ◽  
R.S. Buxton
Keyword(s):  
Escherichia Coli ◽  
Escherichia Coli K12 ◽  
Deo Operon

Kasugamycin inhibition of nonsense suppression by thymine-requiring strains of Escherichia coli K12

1993 ◽  
Vol 39 (4) ◽  
pp. 448-450 ◽  
Author(s):  
E. Tiganos ◽  
M. B. Herrington
Keyword(s):  
Escherichia Coli ◽  
Thymidylate Synthase ◽  
Aminoglycoside Antibiotic ◽  
Nonsense Suppression ◽  
Resistance Mutations ◽  
Escherichia Coli K12 ◽  
Translational Accuracy ◽  
Frame Shift

Thymine-requiring strains of Escherichia coli suppress nonsense and frame-shift mutations. This appears to occur during translation, suggesting that the lack of activity of an enzyme thymidylate synthase, required for the synthesis of a DNA precursor, alters the fidelity of translation. The aminoglycoside antibiotic kasugamycin, which enhances translational accuracy in vitro, prevents thymine-requiring cells from suppressing. The inhibition of suppression by kasugamycin is not prevented by the introduction of two different kasugamycin-resistance mutations, although the dose required for inhibition increases. These observations support the conclusion that suppression occurs during translation.Key words: suppression, kasugamycin, translation, thymine-requiring.

scholarly journals Purification and some properties of nitrate reductase (EC 1.7.99.4) from Escherichia coli K12

1976 ◽  
Vol 153 (3) ◽  
pp. 533-541 ◽  
Author(s):  
R A Clegg
Keyword(s):  
Escherichia Coli ◽  
Aqueous Solution ◽  
Nitrate Reductase ◽  
Cell Envelope ◽  
Purification Procedure ◽  
Benzyl Viologen ◽  
Escherichia Coli K12 ◽  
Enzyme Subunits ◽  
Triton X

1. Nitrate reductase was purified 134-fold from Escherichia coli K12. The purification procedure involves the release by Triton X-100 of the enzyme from the cell envelope. i. The purified enzyme exists in aqueous solution either as a monomer (mol. wt. about 220 000) or as an associated form (probably a tetramer; mol.wt. about 880 000). 3. The purified enzyme has three subunits with apparent mol.wts. of 150 000, 67000 and 65000. An additional subunit of apparent mol.wt. 20000 is present in a haem-containing fraction that is also produced by the preparative procedure described. 4. None of the enzyme subunits is present in the cell envelope of cells grown in the absence of nitrate. 5. Reversible changes in the activity of nitrate reductase in vitro with FMNH2 as reductant can be induced under circumstances which are without effect on the reduced Benzyl Viologen-NO3-activity.

Studies in vitro of the Enzyme Controlled by the recB and recC Genes of Escherichia coli K12

1973 ◽  
Vol 1 (1) ◽  
pp. 237-238
Author(s):  
STUART LINN ◽  
ALEXANDER E. KARU ◽  
PETER J. GOLDMARK
Keyword(s):  
Escherichia Coli ◽  
Escherichia Coli K12

A possible mechanism for the in vitro activation of L-serine deaminase activity in Escherichia coli K12

1990 ◽  
Vol 68 (4) ◽  
pp. 723-728 ◽  
Author(s):  
E. B. Newman ◽  
Caroline Walker ◽  
K. Ziegler-Skylakakis
Keyword(s):  
Escherichia Coli ◽  
Enzyme Activation ◽  
Free Radical Scavengers ◽  
Escherichia Coli K12 ◽  
Diethylene Triamine ◽  
In Vitro Activation ◽  
Diethylene Triamine Pentaacetic Acid ◽  
Serine Deaminase ◽  
Reversible Reduction

L-Serine deaminase is inactive in crude extracts of Escherichia coli K12, but can be activated by incubation with iron and dithiothreitol. This activation requires oxygen, and is inhibited by free radical scavengers and by diethylene triamine pentaacetic acid, which prevents Fe cycling. We suggest that in vitro activation of L-serine deaminase is catalyzed by an oxidant (perhaps hydroxyl radicals). Also, activation may be accompanied by a decrease in molecular weight and involve both a cleavage of the polypeptide chain and a reversible reduction of the molecule.Key words: enzyme activation, serine degradation.

scholarly journals Complementation in vitro Between guaB Mutants of Escherichia coli K12

Microbiology ◽  
1980 ◽  
Vol 117 (1) ◽  
pp. 33-45
Author(s):  
H. J. Gilbert ◽  
W. T. Drabble
Keyword(s):  
Escherichia Coli ◽  
Escherichia Coli K12
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