Louw M E, Reid S J, Watson T G
Biotechnology Programme, CSIR, Pretoria, Republic of South Africa.
Appl Microbiol Biotechnol. 1993 Jan;38(4):507-13. doi: 10.1007/BF00242946.
A Bacillus brevis gene coding for an endo-(1,3-1,4)-beta-glucanase was cloned in Escherichia coli and sequenced. The open reading frame contains a sequence of 759 nucleotides encoding a polypeptide of 252 amino acid residues. The amino acid sequence of the beta-glucanase gene showed only a 50% similarity to previously published data for Bacillus endo-(1,3-1,4)-beta-glucanases. The optimum temperature and pH for enzyme activity were 65-70 degrees C and 8-10, respectively. When held at 75 degrees C for 1 h, 75% residual activity was measured. The molecular mass was estimated to be about 29 kDa on sodium dodecyl sulphate (SDS)-polyacrylamide gel electrophoresis and the enzyme was found to be resistant to SDS.
编码一种内切 -(1,3 - 1,4)-β - 葡聚糖酶的短短芽孢杆菌基因在大肠杆菌中被克隆并测序。开放阅读框包含759个核苷酸的序列,编码一个由252个氨基酸残基组成的多肽。β - 葡聚糖酶基因的氨基酸序列与先前发表的短短芽孢杆菌内切 -(1,3 - 1,4)-β - 葡聚糖酶的数据仅显示50%的相似性。酶活性的最适温度和pH分别为65 - 70℃和8 - 10。当在75℃保持1小时时,测得75%的残余活性。在十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳上估计分子量约为29 kDa,并且发现该酶对SDS具有抗性。