1. The Production and Utilization of GDP-glucose in the Biosynthesis of Trehalose 6-Phosphate by Streptomyces venezuelae
- Author
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Farzana Miah, Matías Damián Asención Diez, David M. Lawson, Clare E. M. Stevenson, Stephen Bornemann, and Alberto A. Iglesias
- Subjects
0301 basic medicine ,Streptomyces venezuelae ,crystal structure ,substrate specificity ,Otras Ciencias Biológicas ,030106 microbiology ,Mutant ,medicine.disease_cause ,glycosyltransferase ,Biochemistry ,purl.org/becyt/ford/1 [https] ,Ciencias Biológicas ,03 medical and health sciences ,chemistry.chemical_compound ,ACTINOBACTERIA ,Bacterial Proteins ,Biosynthesis ,Escherichia coli ,medicine ,Transferase ,carbohydrate metabolism ,purl.org/becyt/ford/1.6 [https] ,Molecular Biology ,trehalose ,GDP-GLUCOSE ,Binding Sites ,biology ,microbiology ,Galactose ,Trehalose ,Cell Biology ,biology.organism_classification ,Streptomyces ,GLUCOSYLTRANSFERASE ,chemistry ,Glucosyltransferases ,TREHALOSE-6P ,Guanosine Diphosphate Sugars ,Enzymology ,Sugar Phosphates ,Streptomyces hygroscopicus ,CIENCIAS NATURALES Y EXACTAS - Abstract
Trehalose-6-phosphate synthase OtsA from streptomycetes is unusual in that it uses GDP-glucose as the donor substrate rather than the more commonly used UDP-glucose. We now confirm that OtsA from Streptomyces venezuelae has such a preference for GDP-glucose and can utilize ADP-glucose to some extent too. A crystal structure of the enzyme shows that it shares twin Rossmann-like domains with the UDP-glucose-specific OtsA from Escherichia coli. However, it is structurally more similar to Streptomyces hygroscopicus VldE, a GDP-valienol-dependent pseudoglycosyltransferase enzyme. Comparison of the donor binding sites reveals that the amino acids associated with the binding of diphosphoribose are almost all identical in these three enzymes. By contrast, the amino acids associated with binding guanine in VldE (Asn, Thr, and Val) are similar in S. venezuelae OtsA (Asp, Ser, and Phe, respectively) but not conserved in E. coli OtsA (His, Leu, and Asp, respectively), providing a rationale for the purine base specificity of S. venezuelae OtsA. To establish which donor is used in vivo, we generated an otsA null mutant in S. venezuelae. The mutant had a cell density-dependent growth phenotype and accumulated galactose 1-phosphate, glucose 1-phosphate, and GDP-glucose when grown on galactose. To determine how the GDP-glucose is generated, we characterized three candidate GDP-glucose pyrophosphorylases. SVEN_3027 is a UDP-glucose pyrophosphorylase, SVEN_3972 is an unusual ITP-mannose pyrophosphorylase, and SVEN_2781 is a pyrophosphorylase that is capable of generating GDP-glucose as well as GDP-mannose. We have therefore established how S. venezuelae can make and utilize GDP-glucose in the biosynthesis of trehalose 6-phosphate. Fil: Asención Diez, Matías Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Agrobiotecnología del Litoral. Universidad Nacional del Litoral. Instituto de Agrobiotecnología del Litoral; Argentina Fil: Miah, Farzana. John Innes Institute; Reino Unido Fil: Stevenson, Clare E. M.. John Innes Institute; Reino Unido Fil: Lawson, David M.. John Innes Institute; Reino Unido Fil: Iglesias, Alberto Alvaro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Agrobiotecnología del Litoral. Universidad Nacional del Litoral. Instituto de Agrobiotecnología del Litoral; Argentina Fil: Bornemann, Stephen. John Innes Institute; Reino Unido
- Published
- 2017
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