Jauris-Heipke S, Fuchs R, Hofmann A, Lottspeich F, Preac-Mursic V, Soutschek E, Will G, Wilske B
Abteilung Serologie, Max von Pettenkofer Institute, Munich, FRG.
FEMS Microbiol Lett. 1993 Dec 1;114(2):235-41. doi: 10.1111/j.1574-6968.1993.tb06579.x.
The p100 gene coding for the p100 protein of Borrelia burgdorferi strain PKo has been cloned, sequenced and expressed in Escherichia coli. An open reading frame including upstream and downstream sequences with potential translation and transcription signals could be identified. The reading frame consists of 1989 nucleotides corresponding to a protein of 663 amino acids and a calculated molecular mass of 75.8 kDa. The protein has a leader peptide and is processed without modification at the N-terminus. A high percentage of amino acid sequence identity could be found to the high-molecular mass protein p83/p93 of B. burgdorferi strain B31.
编码伯氏疏螺旋体PKo菌株p100蛋白的p100基因已在大肠杆菌中克隆、测序并表达。可鉴定出一个包含上游和下游序列以及潜在翻译和转录信号的开放阅读框。该阅读框由1989个核苷酸组成,对应于一个663个氨基酸的蛋白质,计算分子量为75.8 kDa。该蛋白质有一个前导肽,在N端未经修饰进行加工。与伯氏疏螺旋体B31菌株的高分子量蛋白p83/p93有很高的氨基酸序列同一性。