Amemura A, Chakraborty R, Fujita M, Noumi T, Futai M
Institute of Scientific and Industrial Research, Osaka University, Japan.
J Biol Chem. 1988 Jul 5;263(19):9271-5.
The gene (iam) coding for isoamylase (glycogen 6-glucanohydrolase) of Pseudomonas amyloderamosa SB-15 was cloned. Its nucleotide sequence contained an open reading frame of 2313 nucleotides (771 amino acids) encoding a precursor of secreted isoamylase. The precursor contained a signal peptide of 26 amino acid residues at its amino terminus and three regions homologous with those conserved in alpha-amylases (1,4-alpha-D-glucan 4-glucanohydrolase) of species ranging from prokaryotes to eukaryotes. These homologous regions were also found in another debranching enzyme, pullulanase (pullulan 6-glucanohydrolase) from Klebsiella aerogenes. Sequences of the isoamylase also showed significant homology with those between positions 300 and the carboxyl terminus of pullulanase. The regions required for the specificity of isoamylase were discussed on the basis of a comparison of its amino acid sequence with those of alpha-amylases, cyclomaltodextrin glucanotransferases, and pullulanase.
克隆了编码解淀粉假单胞菌SB - 15中异淀粉酶(糖原6 - 葡聚糖水解酶)的基因(iam)。其核苷酸序列包含一个2313个核苷酸的开放阅读框(771个氨基酸),编码分泌型异淀粉酶的前体。该前体在其氨基末端含有一个26个氨基酸残基的信号肽,以及三个与从原核生物到真核生物的α - 淀粉酶(1,4 - α - D - 葡聚糖4 - 葡聚糖水解酶)中保守区域同源的区域。这些同源区域也存在于另一种脱支酶,产气克雷伯菌的支链淀粉酶(支链淀粉6 - 葡聚糖水解酶)中。异淀粉酶的序列与支链淀粉酶300位至羧基末端之间的序列也显示出显著的同源性。基于异淀粉酶氨基酸序列与α - 淀粉酶、环糊精葡聚糖转移酶和支链淀粉酶的氨基酸序列比较,讨论了异淀粉酶特异性所需的区域。