Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
20
pubmed:dateCreated
1996-12-3
pubmed:abstractText
The fermentative alcohol dehydrogenase of Escherichia coli is encoded by the adhE gene, which is induced under anaerobic conditions but repressed in air. Previous work suggested that induction of adhE might depend on NADH levels. We therefore directly measured the NAD+ and NADH levels for cultures growing aerobically and anaerobically on a series of carbon sources whose metabolism generates different relative amounts of NADH. Expression of adhE was monitored both by assay of alcohol dehydrogenase activity and by expression of phi(adhE'-lacZ) gene fusions. The expression of the adhE gene correlated with the ratio of NADH to NAD+. The role of NADH in eliciting adhE induction was supported by a variety of treatments known to change the ratio of NADH to NAD+ or alter the total NAD+-plus-NADH pool. Blocking the electron transport chain, either by mutation or by chemical inhibitors, resulted in the artificial induction of the adhE gene under aerobic conditions. Conversely, limiting NAD synthesis, by introducing mutational blocks into the biosynthetic pathway for nicotinic acid, decreased the expression of adhE under anaerobic conditions. This, in turn, was reversed by supplementation with exogenous NAD or nicotinic acid. In merodiploid strains carrying deletion or insertion mutations abolishing the synthesis of AdhE protein, an adhE-lacZ fusion was expressed at nearly 10-fold the level observed in an adhE+ background. Introduction of mutant adhE alleles producing high levels of inactive AdhE protein gave results equivalent to those seen in absence of the AdhE protein. This finding implies that it is the buildup of NADH due to lack of enzyme activity, rather than the absence of the AdhE protein per se, which causes increased induction of the phi(adhE'-lacZ) fusion. Moreover, mutations giving elevated levels of active AdhE protein decreased the induction of the phi(adhE'-lacZ) fusion. This finding suggests that the enzymatic activity of the AdhE protein modulates the level of NADH under anaerobic conditions, thus indirectly regulating its own expression.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-1325457, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-13278318, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-1328158, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-16348821, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-1999382, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-2015910, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-2681156, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-2695398, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-2698228, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-3116274, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-3522551, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-3550385, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-3934331, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-4351948, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-4360220, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-4379647, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-4381873, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-4392484, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-4553845, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-5432063, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-5459938, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-6339476, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-6387427, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-6418721, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-6752127, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-6986356, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-7961393, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-796666, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-8113186, http://linkedlifedata.com/resource/pubmed/commentcorrection/8830700-8423158
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0021-9193
pubmed:author
pubmed:issnType
Print
pubmed:volume
178
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6013-8
pubmed:dateRevised
2010-9-13
pubmed:meshHeading
pubmed:year
1996
pubmed:articleTitle
Role of NAD in regulating the adhE gene of Escherichia coli.
pubmed:affiliation
Department of Microbiology, Southern Illinois University, Carbondale 62901, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S.