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PmST3 from Pasteurella multocida encoded by Pm1174 gene is a monofunctional α2–3-sialyltransferase

Applied Microbiology and Biotechnology volume 94, pages 977–985 (2012)Cite this article

Abstract

Pasteurella multocida (Pm) strain Pm70 has three putative sialyltransferase genes including Pm0188, Pm0508, and Pm1174. A Pm0188 gene homolog in Pm strain P-1059 encodes a multifunctional α2–3-sialyltransferase, PmST1, that prefers oligosaccharide acceptors. A Pm0508 gene homolog in the same strain encodes a monofunctional sialyltransferase PmST2 that prefers glycolipid acceptors. Here, we report that the third sialyltransferase from Pm (PmST3) encoded by gene Pm1174 in strain Pm70 is a monofunctional α2–3-sialyltransferase that can use both oligosaccharides and glycolipids as efficient acceptors. Despite the existence of both Pm0188 and Pm0508 gene homologs encoding PmST1 and PmST2, respectively, in Pm strain P-1059, a Pm1174 gene homolog appears to be absent from Pm strains P-1059 and P-934. PmST3 was successfully obtained by cloning and expression using a synthetic gene of Pm1174 with codons optimized for Escherichia coli expression system as the DNA template for polymer chain reactions. Truncation of 35 amino acid residues from the carboxyl terminus was shown to improve the expression of a soluble and active enzyme in E. coli as a C-His6-tagged fusion protein. This sialidase-free monofunctional α2–3-sialyltransferase is a useful tool for synthesizing sialylated oligosaccharides and glycolipids.

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Acknowledgments

This work was support by NSF grant CHE1012511, NIH grant R01HD065122, the Camille Dreyfus Teacher-Scholarship, and the UC-Davis Chancellor's Fellowship.

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  1. Department of Chemistry, University of California, One Shields Avenue, Davis, CA, 95616, USA

    Vireak Thon, Yanhong Li, Hai Yu, Kam Lau & Xi Chen

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  1. Vireak Thon
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  2. Yanhong Li
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  3. Hai Yu
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  4. Kam Lau
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Correspondence to Xi Chen.

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Thon, V., Li, Y., Yu, H. et al. PmST3 from Pasteurella multocida encoded by Pm1174 gene is a monofunctional α2–3-sialyltransferase. Appl Microbiol Biotechnol 94, 977–985 (2012). https://doi.org/10.1007/s00253-011-3676-6

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  • DOI: https://doi.org/10.1007/s00253-011-3676-6

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