4.6 Article

Escherichia coli YrbH is a D-Arabinose 5-phosphate isomerase

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JOURNAL OF BIOLOGICAL CHEMISTRY
卷 278, 期 35, 页码 32771-32777

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AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M303661200

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  1. NIGMS NIH HHS [GM 53069] Funding Source: Medline

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A gene encoding for arabinose 5-phosphate isomerase (API), which catalyzes the interconversion of D-ribulose 5-phosphate (Ru5P) and D-arabinose 5-phosphate (A5P), has been identified from the genome of Escherichia coli K-12. API is the first enzyme in the biosynthesis of 3-deoxy-D-manno- octulosonate (KDO), a sugar moiety located in the lipopolysaccharide layer of most Gram-negative bacteria. The API gene yrbH is located next to the recently identified specific KDO 8-P phosphatase gene, yrbI. The 328-amino acid open reading frame yrbH was cloned, overexpressed, and characterized. The purified recombinant enzyme is a tetramer and is sensitive to inhibition by zinc cations. API has optimal activity at pH 8.4 and catalytic residues with estimated pK(a) values of 6.55 +/- 0.04 and 10.34 +/- 0.07. The enzyme is specific for A5P and Ru5P, with apparent K-m values of 0.61 +/- 0.06 mM for A5P and 0.35 +/- 0.08 mM for Ru5P. The apparent k(cat) in the A5P to Ru5P direction is 157 +/- 4 s(-1), and in the Ru5P to A5P direction it is 255 +/- 16 s(-1). The value of K-eq (Ru5P/A5P) is 0.50 +/- 0.06. Homology searches of the E. coli genome suggest yrbH may be one of multiple genes that encode proteins with API activity.

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