Signal transduction through the AtoS-AtoC/az two component system towards poly (3-OH-butyrate) biosynthesis in E. coli

see the original item page
in the repository's web site and access all digital files if the item*



Signal transduction through the AtoS-AtoC/az two component system towards poly (3-OH-butyrate) biosynthesis in E. coli

Panagiotidis, C.A.
Theodorou, E.C.
Kyriakidis, D.A.

The AtoS-AtoC/Az two-component system activates the ato- DAEB operon expression upon acetoacetate induction for E. coli growth in short-chain fatty acids. It also enhances the poly (3- OH-butyrate) (cPHB) biosynthesis, upon acetoacetate induction as well as in the presence of spermidine. The response regulator of the system is the antizyme (Az) of ornithine decarboxylase and is the product of atoC gene. It belongs to the NtrC-NifA family of sigma54-RNA polymerase transcriptional activators. AtoC contains two putative phosphorylation sites, i.e. a conserved aspartic acid among the response regulators and a histidine residue in an H box consensus sequence, normally common to histidine kinases. We report here, that only phosphorylationcompetent AtoC can lead to enhanced production of cPHB in E. coli, when overexpressed with AtoS. Specifically, upon acetoacetate induction, the mutation of Asp reduces cPHB accumulation, compared with cells expressing wild-type AtoC. The mutation of His residue has an even more pronounced effect. The relative effects of these mutations on cPHB accumulation are consistent with their effects on atoDAEB operon expression, i.e. the mutation of Asp has a more potent phenotype than the substitution of His, in the presence of spermidine. Introduction of both AtoC mutations render the system unresponsive to acetoacetate as well as polyamine, resulting in total abrogation of the AtoS-AtoC/Az overexpression effect phenotype to cPHB levels in E. coli.

ConferenceItem


English

2010-04-27T11:00:25Z
2006
2012-06-12T12:23:30Z

http://hdl.handle.net/10442/8344
DOI: http://dx.doi.org/10.1111/j.1742-4658.2006.05277.x


Τύποι Τεκμηρίων
Άλλες Συλλογές
Συλλογές του Ήλιος
Τεκμήριο Συνεδρίου




*Institutions are responsible for keeping their URLs functional (digital file, item page in repository site)