Distinct substrate specificities of three glycoside hydrolase family 42 beta-galactosidases from Bifidobacterium longum subsp infantis ATCC 15697

作者：Viborg Alexander H; Katayama Takane; Abou Hachem Maher; Andersen Mathias C F; Nishimoto Mamoru; Clausen Mads H; Urashima Tadasu; Svensson Birte^*; Kitaoka Motomitsu

来源：Glycobiology, 2014, 24(2): 208-216.

DOI：10.1093/glycob/cwt104

• galactooligosaccharides
• phylogenetic tree
• prebiotics
• probiotics
• sequence motifs

Glycoside hydrolase family 42 (GH42) includes beta-galactosidases catalyzing the release of galactose (Gal) from the non-reducing end of different beta-d-galactosides. Health-promoting probiotic bifidobacteria, which are important members of the human gastrointestinal tract microbiota, produce GH42 enzymes enabling utilization of beta-galactosides exerting prebiotic effects. However, insight into the specificity of individual GH42 enzymes with respect to substrate monosaccharide composition, glycosidic linkage and degree of polymerization is lagging. Kinetic analysis of natural and synthetic substrates resembling various milk and plant galactooligosaccharides distinguishes the three GH42 members, Bga42A, Bga42B and Bga42C, encoded by the probiotic B. longum subsp. infantis ATCC 15697 and revealed the glycosyl residue at subsite +1 and its linkage to the terminal Gal at subsite -1 to be key specificity determinants. Bga42A thus prefers the beta 1-3-galactosidic linkage from human milk and other beta 1-3- and beta 1-6-galactosides with glucose or Gal situated at subsite +1. In contrast, Bga42B very efficiently hydrolyses 4-galactosyllactose (Gal beta 1-4Gal beta 1-4Glc) as well as 4-galactobiose (Gal beta 1-4Gal) and 4-galactotriose (Gal beta 1-4Gal beta 1-4Gal). The specificity of Bga42C resembles that of Bga42B, but the activity was one order of magnitude lower. Based on enzyme kinetics, gene organization and phylogenetic analyses, Bga42C is proposed to act in the metabolism of arabinogalactan-derived oligosaccharides. The distinct kinetic signatures of the three GH42 enzymes correlate to unique sequence motifs denoting specific clades in a GH42 phylogenetic tree providing novel insight into GH42 subspecificities. Overall, the data illustrate the metabolic adaptation of bifidobacteria to the beta-galactoside-rich gut niche and emphasize the importance and diversity of beta-galactoside metabolism in probiotic bifidobacteria.

• 出版日期2014-2