Sequence and structure‐based prediction of fructosyltransferase activity for functional subclassification of fungal GH32 enzymes. (22nd October 2015) - Trollope, Kim M.
Abstract : Sucrolytic enzymes catalyse sucrose hydrolysis or the synthesis of fructooligosaccharides (FOSs), a prebiotic in human and animal nutrition. FOS synthesis capacity differs between sucrolytic enzymes. Amino‐acid‐sequence‐based classification of FOS synthesizing enzymes would greatly facilitate the in silico identification of novel catalysts, as large amounts of sequence data lie untapped. The development of a bioinformatics tool to rapidly distinguish between high‐level FOSs synthesizing predominantly sucrose hydrolysing enzymes from fungal genomic data is presented. Sequence comparison of functionally characterized enzymes displaying low‐ and high‐level FOS synthesis revealed conserved motifs unique to each group. New light is shed on the sequence context of active site residues in three previously identified conserved motifs. We characterized two enzymes predicted to possess low‐ and high‐level FOS synthesis activities based on their conserved motif sequences. FOS data for the enzymes confirmed our successful prediction of their FOS synthesis capacity. Structural comparison of enzymes displaying low‐ and high‐level FOS synthesis identified steric hindrance between nystose and a long loop region present only in low‐level FOS synthesizers. This loop is proposed to limit the synthesis of FOS species with higher degrees of polymerization, a phenomenon observed among enzymes displaying low‐level FOS synthesis. Conserved sequence motifs surrounding catalytic residues and a distant structural determinant were identifiers of FOS synthesis capacity and allow for functional annotation of sucrolytic enzymes directly from amino acid sequence. The tool presented may also be useful to study the structure–function relationships of β‐fructofuranosidases by identifying mutations present in a group of closely related enzymes displaying similar function. Abstract : An experimentally validated bioinformatic tool is presented to facilitate the rapid functional sub‐classification of glycosyl hydrolase family 32 sucrolytic enzymes from protein sequence. Identification of conserved sequence motifs and a structural loop classifies enzymes as possessing either high or low‐level fructooligosaccharide synthetic capacity. Prebiotic fructooligosaccharides are synthesised from sucrose and their consumption is linked to improved human and animal health.