Dept. of Marine Biotechnology, Fukuyama Univ., 1-985 Sanzo, Higashimura-cho, Fukuyama, Hiroshima 729-0292, Japan.
J Food Sci. 2018 May;83(5):1208-1214. doi: 10.1111/1750-3841.14125. Epub 2018 Apr 6.
β-N-Acetylhexosaminidase was identified from Bacillus sp. CH11 and found to have relatively high transferring activity. In this study, its enzymatic properties and transglycosylation activity including its acceptor specificity were investigated. Its molecular weight was estimated to be 90 kDa by SDS-PAGE and its optimal pH was approximately 7 with good stability from pH 6 to 8. Its optimal temperature was 40 °C, and its activity was stable at temperatures of up to 40 °C. To analyze its acceptor specificity for transglycosylation, N, N'-diacetylchitobiose was used as a donor substrate and alcohols, sugar alcohols, sugars and polyphenols were used as acceptors. Dialcohols, which have 2 hydroxyl groups on the outside of the carbon chains, were good acceptors. The molecular size of the acceptor did not influence the transglycosylation up to at least 1,5-pentanediol (carbon number: C5). Glycerin (C3), erythritol (C4), and xylitol (C5), all small molecular weight sugar alcohols, had high acceptor specificity. Transglycosylation to mono- and disaccharides and polyphenols was not observed except for L-fucose. For the β-N-acetylhexosaminidase-catalyzed transglycosylation of chitin oligosaccharides and xylitol, the transfer product was identified as 1-O-β-D-N-acetylglucosaminyl xylitol. The optimal ratio of xylitol was 24% to 2% N, N'-diacetylchitobiose and 226 mg per 1 g N, N'-diacetylchitobiose was produced. CH11 β-N-acetylhexosaminidase efficiently produced 1-O-β-D-N-acetylglucosaminyl xylitol via transglycosylation.
The new transfer products including 1-O-β-D-N-acetylglucosaminyl xylitol are attractive compounds for their potential physiological functions. 1-O-β-D-N-Acetylglucosaminyl xylitol was produced effectively from chitin-oligosaccharides and xylitol by β-N-acetylhexosaminidase from Bacillus sp. CH11. This enzyme may be useful for the development of food materials for health-related applications such as oligosaccharides with intestinal functions and noncariogenic sugars.
从芽孢杆菌 CH11 中鉴定出 β-N-乙酰氨基葡萄糖苷酶,发现其具有相对较高的转移活性。在这项研究中,研究了其酶学性质和转糖基活性,包括其受体特异性。其分子量通过 SDS-PAGE 估计为 90 kDa,最适 pH 约为 7,在 pH6 到 8 之间具有良好的稳定性。最适温度为 40°C,其活性在高达 40°C 的温度下稳定。为了分析其转糖基反应的受体特异性,使用 N,N'-二乙酰壳二糖作为供体底物,使用醇、糖醇、糖和多酚作为受体。具有碳链外侧 2 个羟基的二醇是良好的受体。受体的分子大小在至少 1,5-戊二醇(碳原子数:C5)下不影响转糖基化。甘油(C3)、赤藓糖醇(C4)和木糖醇(C5)等小分子糖醇具有很高的受体特异性。除 L-岩藻糖外,未见单糖和二糖以及多酚的转糖基化。对于壳寡糖和木糖醇的β-N-乙酰氨基葡萄糖苷酶催化的转糖基化,转移产物被鉴定为 1-O-β-D-N-乙酰氨基葡萄糖基木糖醇。木糖醇的最佳比例为 24%至 2%N,N'-二乙酰壳二糖,每 1g N,N'-二乙酰壳二糖产生 226mg。CH11 β-N-乙酰氨基葡萄糖苷酶通过转糖基化有效地生成 1-O-β-D-N-乙酰氨基葡萄糖基木糖醇。
包括 1-O-β-D-N-乙酰氨基葡萄糖基木糖醇在内的新的转移产物因其潜在的生理功能而成为有吸引力的化合物。通过芽孢杆菌 CH11 的β-N-乙酰氨基葡萄糖苷酶,从壳寡糖和木糖醇有效生产 1-O-β-D-N-乙酰氨基葡萄糖基木糖醇。该酶可能对开发与健康相关的应用的食品材料有用,例如具有肠道功能的低聚糖和非致龋糖。