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licT [2018-02-10T14:30:04.000Z]
Molecular weight
32.22 kDa
Function
control of beta-glucan and beta-glucoside utilization
Product
transcriptional antiterminator (BglG family)
Genomic Context
Categories containing this gene/protein
Gene
Coordinates
4,012,866 → 4,013,699
Phenotypes of a mutant
The protein
Catalyzed reaction/ biological activity
binding to the mRNAs of bglS and the bglP-bglH operon, causes transcription antitermination (in presence of salicin and absence of glucose) Protein family
BglG family of antiterminators (according to Swiss-Prot)Paralogous protein(s)
Domains
Modification
phosphorylation at His-100 in PRD-1 by phosphorylated BglP, inhibits LicT antitermination activityphosphorylation at His-207 and/or His-269 in PRD-2 by His-P-HPr, stimulates LicT antitermination activity Structure
Localization
cytoplasm, even distribution in the absence of the inducer salicin, subpolar localization in the presence of salicin PubMed Additional information
Expression and Regulation
Biological materials
Mutant
GP427 (ΔlicT-bglS::erm), available in Jörg Stülke's labBKE39080 (ΔlicT::erm trpC2) available at BGSC, PubMed, upstream reverse: _UP1_CATGGCATGTCCCTCCAAAT, downstream forward: _UP4_TAATGAGAGCGCTGACATTTBKK39080 (ΔlicT::kan trpC2) available at BGSC, PubMed, upstream reverse: _UP1_CATGGCATGTCCCTCCAAAT, downstream forward: _UP4_TAATGAGAGCGCTGACATTT Expression vector
for expression, purification of both PRDs in E. coli with N-terminal His-tag, in pWH844: pGP165, available in Jörg Stülke's labfor expression, purification of the RNA-binding domain in E. coli with N-terminal His-tag, in pWH844: pGP315, available in Jörg Stülke's labfor expression, purification of the RNA-binding domain in E. coli with N-terminal His-tag and thrombin cleavage site, in pGP570: pGP572, available in Jörg Stülke's lab GFP fusion
FLAG-tag construct
Labs working on this gene/protein
Stephane Aymerich, Microbiology and Molecular Genetics, INRA Paris-Grignon, FranceJosef Deutscher, Microbiology and Molecular Genetics, INRA Paris-Grignon, France References
Reviews
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Original publications
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