scispace - formally typeset
Journal ArticleDOI

A multifunctional Pasteurella multocida sialyltransferase: a powerful tool for the synthesis of sialoside libraries.

TLDR
A multifunctional sialyltransferase has been cloned from Pasteurella multocida strain P-1059 and expressed in E. coli as a truncated C-terminal His6-tagged recombinant protein (tPm0188Ph).
Abstract
A multifunctional sialyltransferase has been cloned from Pasteurella multocida strain P-1059 and expressed in E. coli as a truncated C-terminal His6-tagged recombinant protein (tPm0188Ph). Biochemical studies indicate that the obtained protein is (1) an alpha2,3-sialyltransferase (main function), (2) an alpha2,6-sialyltransferase, (3) an alpha2,3-sialidase, and (4) an alpha2,3-trans-sialidase. The recombinant tPm0188Ph is a powerful tool in the synthesis of structurally diverse sialoside libraries due to its relaxed substrate specificity, high solubility, high expression level, and multifunctionality.

read more

Citations
More filters
Journal ArticleDOI

Glycosyltransferases: structures, functions, and mechanisms.

TL;DR: The expected two-step double-displacement mechanism is rendered less likely by the lack of conserved architecture in the region where a catalytic nucleophile would be expected, and a mechanism involving a short-lived oxocarbenium ion intermediate now seems the most likely, with the leaving phosphate serving as the base.
Journal ArticleDOI

Advances in the Biology and Chemistry of Sialic Acids

TL;DR: A large library of sialoside standards and derivatives in amounts sufficient for structure-activity relationship studies are provided and sialoglycan microarrays provide an efficient platform for quick identification of preferred ligands for sialic acid-binding proteins.
Journal ArticleDOI

Pasteurella multocida pathogenesis: 125 years after Pasteur

TL;DR: Pasteurella multocida was first shown to be the causative agent of fowl cholera by Louis Pasteur in 1881 and a number of other virulence factors have been identified by both directed and random mutagenesis, including PMT, putative surface adhesins and iron acquisition proteins.
Journal ArticleDOI

Diversity in specificity, abundance, and composition of anti-Neu5Gc antibodies in normal humans: Potential implications for disease

TL;DR: It is suggested that this ongoing antigen-antibody reaction may generate chronic inflammation, possibly contributing to the high frequency of diet-related carcinomas and other diseases in humans.
Journal ArticleDOI

Enzymatic labeling of proteins: techniques and approaches

TL;DR: This review article summarizes the enzymatic strategies, which enable site-specific functionalization of proteins with a variety of different functional groups, which include formylglycine generating enzyme, sialyl transferases, phosphopantetheinyltransferases, O-GlcNAc post-translational modification, sortagging, transglutaminase, farnesyltransferase, biotin ligase, lipoic acid ligase and N-myristoyltransferase
References
More filters
Journal ArticleDOI

Cell Surface Engineering by a Modified Staudinger Reaction

TL;DR: A chemical transformation that permits the selective formation of covalent adducts among richly functionalized biopolymers within a cellular context is presented and should permit its execution within a cell's interior, offering new possibilities for probing intracellular interactions.
Journal ArticleDOI

Enzymes for chemical synthesis

TL;DR: Enzyme-catalysed chemical transformations are now widely recognized as practical alternatives to traditional (non-biological) organic synthesis, and as convenient solutions to certain intractable synthetic problems.
Journal ArticleDOI

Achievements and challenges of sialic acid research.

TL;DR: The present state of knowledge in sialobiology, with an emphasis on my personal experience in this research area, is outlined including a discussion of necessary future work in this fascinating field of cell biology.
Journal ArticleDOI

Synthesis of sugar arrays in microtiter plate.

TL;DR: 1,3-Dipolar cycloadditions between azides and alkynes were exploited to attach oligosaccharides to a C(14) hydrocarbon chain that noncovalently binds to the microtiter well surface to achieve biotransformation of beta-galactosyllipid 5.
Related Papers (5)