Willems A, East A K, Lawson P A, Collins M D
Department of Microbiology, AFRC Institute of Food Research, Reading, UK.
Res Microbiol. 1993 Sep;144(7):547-56. doi: 10.1016/0923-2508(93)90004-l.
The neurotoxin gene from a strain of Clostridium botulinum type A causing infant botulism was cloned as a series of overlapping polymerase chain reaction (PCR) fragments generated using primers designed to conserved regions of published botulinal toxin (BoNT) sequences. Translation of the nucleotide sequence derived from cloned PCR fragments demonstrated that the toxin gene encodes a protein of 1,296 amino acid residues. Comparative alignment of the derived infant BoNT/A sequence with those of other published neurotoxins revealed highest sequence relatedness with BoNT/A of classical food-borne botulism. The sequence identity between infant and classical BoNT/A was 94.9% for the light chain (corresponding to 23 amino acid changes) and 87.1% for the heavy chain (corresponding to 109 amino acid changes).
一株引起婴儿肉毒中毒的A型肉毒梭菌的神经毒素基因,通过使用针对已发表肉毒毒素(BoNT)序列保守区域设计的引物产生的一系列重叠聚合酶链反应(PCR)片段进行克隆。对克隆的PCR片段所得核苷酸序列的翻译表明,该毒素基因编码一个由1296个氨基酸残基组成的蛋白质。将所得婴儿BoNT/A序列与其他已发表神经毒素的序列进行比对,结果显示与经典食源性肉毒中毒的BoNT/A序列相关性最高。婴儿型和经典型BoNT/A轻链的序列同一性为94.9%(相当于23个氨基酸变化),重链的序列同一性为87.1%(相当于109个氨基酸变化)。