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http://purl.uniprot.org/citations/23634833http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23634833http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23634833http://www.w3.org/2000/01/rdf-schema#comment"

Background

The catabolic pathways of N-acetyl-D-galactosamine (Aga) and D-galactosamine (Gam) in E. coli were proposed from bioinformatic analysis of the aga/gam regulon in E. coli K-12 and later from studies using E. coli C. Of the thirteen genes in this cluster, the roles of agaA, agaI, and agaS predicted to code for Aga-6-P-deacetylase, Gam-6-P deaminase/isomerase, and ketose-aldolase isomerase, respectively, have not been experimentally tested. Here we study their roles in Aga and Gam utilization in E. coli O157:H7 and in E. coli C.

Results

Knockout mutants in agaA, agaI, and agaS were constructed to test their roles in Aga and Gam utilization. Knockout mutants in the N-acetylglucosamine (GlcNAc) pathway genes nagA and nagB coding for GlcNAc-6-P deacetylase and glucosamine-6-P deaminase/isomerase, respectively, and double knockout mutants ΔagaA ΔnagA and ∆agaI ∆nagB were also constructed to investigate if there is any interplay of these enzymes between the Aga/Gam and the GlcNAc pathways. It is shown that Aga utilization was unaffected in ΔagaA mutants but ΔagaA ΔnagA mutants were blocked in Aga and GlcNAc utilization. E. coli C ΔnagA could not grow on GlcNAc but could grow when the aga/gam regulon was constitutively expressed. Complementation of ΔagaA ΔnagA mutants with either agaA or nagA resulted in growth on both Aga and GlcNAc. It was also found that ΔagaI, ΔnagB, and ∆agaI ΔnagB mutants were unaffected in utilization of Aga and Gam. Importantly, ΔagaS mutants were blocked in Aga and Gam utilization. Expression analysis of relevant genes in these strains with different genetic backgrounds by real time RT-PCR supported these observations.

Conclusions

Aga utilization was not affected in ΔagaA mutants because nagA was expressed and substituted for agaA. Complementation of ΔagaA ΔnagA mutants with either agaA or nagA also showed that both agaA and nagA can substitute for each other. The ∆agaI, ∆nagB, and ∆agaI ∆nagB mutants were not affected in Aga and Gam utilization indicating that neither agaI nor nagB is involved in the deamination and isomerization of Gam-6-P. We propose that agaS codes for Gam-6-P deaminase/isomerase in the Aga/Gam pathway."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.org/dc/terms/identifier"doi:10.1186/1471-2180-13-94"xsd:string
http://purl.uniprot.org/citations/23634833http://purl.org/dc/terms/identifier"doi:10.1186/1471-2180-13-94"xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/author"Hu Z."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/author"Hu Z."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/author"Mukherjee A."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/author"Mukherjee A."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/author"Patel I.R."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/author"Patel I.R."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/name"BMC Microbiol."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/name"BMC Microbiol."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/pages"94"xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/pages"94"xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/title"Genetic analysis of the roles of agaA, agaI, and agaS genes in the N-acetyl-D-galactosamine and D-galactosamine catabolic pathways in Escherichia coli strains O157:H7 and C."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/title"Genetic analysis of the roles of agaA, agaI, and agaS genes in the N-acetyl-D-galactosamine and D-galactosamine catabolic pathways in Escherichia coli strains O157:H7 and C."xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/volume"13"xsd:string
http://purl.uniprot.org/citations/23634833http://purl.uniprot.org/core/volume"13"xsd:string
http://purl.uniprot.org/citations/23634833http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23634833
http://purl.uniprot.org/citations/23634833http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23634833
http://purl.uniprot.org/citations/23634833http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23634833
http://purl.uniprot.org/citations/23634833http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23634833
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