Escherichia coli glycogen genes are organized in a single glgBXCAP transcriptional unit possessing an alternative suboperonic promoter within glgC that directs glgAP expression.
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Systematic production of inactivating and non-inactivating suppressor mutations at the relA locus that compensate the detrimental effects of complete spot loss and affect glycogen content in Escherichia coliBacterial syntenies: an exact approach with gene quorum.Characterization of aberrant pathways across human cancersIdentification of key regulators in glycogen utilization in E. coli based on the simulations from a hybrid functional Petri net model.HPLC-MS/MS analyses show that the near-Starchless aps1 and pgm leaves accumulate wild type levels of ADPglucose: further evidence for the occurrence of important ADPglucose biosynthetic pathway(s) alternative to the pPGI-pPGM-AGP pathwayComparative genomic and phylogenetic analyses of Gammaproteobacterial glg genes traced the origin of the Escherichia coli glycogen glgBXCAP operon to the last common ancestor of the sister orders Enterobacteriales and Pasteurellales.Influence of in situ progressive N-terminal is still controversial truncation of glycogen branching enzyme in Escherichia coli DH5α on glycogen structure, accumulation, and bacterial viabilityGenetic and isotope ratio mass spectrometric evidence for the occurrence of starch degradation and cycling in illuminated Arabidopsis leaves.Phylogenetic diversification and developmental implications of poly-(R)-3-hydroxyalkanoate gene cluster assembly in prokaryotes.Molecular characterization of arginine deiminase pathway in Laribacter hongkongensis and unique regulation of arginine catabolism and anabolism by multiple environmental stresses.The α-glucan phosphorylase MalP of Corynebacterium glutamicum is subject to transcriptional regulation and competitive inhibition by ADP-glucose.A sensitive method for confocal fluorescence microscopic visualization of starch granules in iodine stained samples.Enhancing sucrose synthase activity results in increased levels of starch and ADP-glucose in maize (Zea mays L.) seed endosperms.GlgS, described previously as a glycogen synthesis control protein, negatively regulates motility and biofilm formation in Escherichia coli.A cAMP/CRP-controlled mechanism for the incorporation of extracellular ADP-glucose in Escherichia coli involving NupC and NupG nucleoside transporters
P2860
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P2860
Escherichia coli glycogen genes are organized in a single glgBXCAP transcriptional unit possessing an alternative suboperonic promoter within glgC that directs glgAP expression.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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name
Escherichia coli glycogen gene ...... that directs glgAP expression.
@en
Escherichia coli glycogen gene ...... that directs glgAP expression.
@nl
type
label
Escherichia coli glycogen gene ...... that directs glgAP expression.
@en
Escherichia coli glycogen gene ...... that directs glgAP expression.
@nl
prefLabel
Escherichia coli glycogen gene ...... that directs glgAP expression.
@en
Escherichia coli glycogen gene ...... that directs glgAP expression.
@nl
P2093
P2860
P50
P356
P1433
P1476
Escherichia coli glycogen gene ...... that directs glgAP expression
@en
P2093
Alejandro M Viale
Edurne Baroja-Fernández
Gustavo Eydallin
Manuel Montero
Mehdi Rahimpour
P2860
P304
P356
10.1042/BJ20101186
P407
P577
2011-01-01T00:00:00Z