Song K B, Lee S K, Joo H K, Rhee S K
Applied Microbiology Research Group, Genetic Engineering Research Institute, KIST, Taejon, South Korea.
Biochim Biophys Acta. 1994 Sep 13;1219(1):163-6. doi: 10.1016/0167-4781(94)90262-3.
DNA sequence analysis of a previously cloned 4.5 kb DNA fragment showed that the extracellular sucrase gene (invB) of Zymomonas mobilis was located in the 155 bp downstream of levansucrase gene (levU). The invB gene had an open reading frame of 1242 bp and the deduced amino acid sequence was 413 residues with a molecular weight of 46,107. The translated sequence of Z. mobilis invB was in good agreement with the 10 N-terminal amino acid residues determined by amino acid sequencing. The amino acid sequence of sucrase showed low similarity with that of other sucrases, but higher similarity with that of levansucrases.
对先前克隆的一个4.5 kb DNA片段进行的DNA序列分析表明,运动发酵单胞菌的胞外蔗糖酶基因(invB)位于果聚糖蔗糖酶基因(levU)下游155 bp处。invB基因有一个1242 bp的开放阅读框,推导的氨基酸序列为413个残基,分子量为46107。运动发酵单胞菌invB的翻译序列与通过氨基酸测序确定的10个N端氨基酸残基高度一致。蔗糖酶的氨基酸序列与其他蔗糖酶的相似性较低,但与果聚糖蔗糖酶的相似性较高。