Wiker H G, Michell S L, Hewinson R G, Spierings E, Nagai S, Harboe M
Institute of Immunology and Rheumatology, University of Oslo, N-0172 Oslo, Norway.
Microb Pathog. 1999 Apr;26(4):207-19. doi: 10.1006/mpat.1998.0267.
Based on our N -terminal amino acid sequence of MPT53 and a deduced DNA sequence, we searched for the corresponding gene in the Mycobacterium tuberculosis genomic sequence at the Sanger centre, localizing mpt53 close to mpt70 and mpt83. The gene was cloned and expressed, followed by purification of MPT53 to homogeneity from recombinant M. smegmatis culture fluid. In MPT53 there is 60 % identity with the active site of thioredoxin of M. tuberculosis (MPT46) with two cysteins in a CXXC motif, but MPT53 could not serve as an alternative substrate for thioredoxin reductase. Testing for IgM and IgG1 anti-MPT53 in cattle sera showed that MPT53 is immunogenic following natural and experimental infection with M. bovis. Cloning of mpt53 represents cloning of the last of the 10 proteins originally defined as "secreted proteins" of M. tuberculosis and M. bovis based on determination of their "Localization index" (LI) (J Gen Microbiol 1991;137 : 875-84). The need for a precise definition of the term "secreted protein" is discussed. So far we have observed full concordance between occurrence of an LI value indicating secretion of a protein and occurrence of a signal sequence in the corresponding gene. Signal sequence independent protein secretion in mycobacteria may occur for a limited number of proteins and remains to be established.
基于MPT53的N端氨基酸序列和推导的DNA序列,我们在桑格中心的结核分枝杆菌基因组序列中搜索相应基因,将mpt53定位在靠近mpt70和mpt83的位置。该基因被克隆并表达,随后从重组耻垢分枝杆菌培养液中纯化出纯度达到均一的MPT53。在MPT53中,与结核分枝杆菌硫氧还蛋白(MPT46)的活性位点有60%的同一性,在CXXC基序中有两个半胱氨酸,但MPT53不能作为硫氧还蛋白还原酶的替代底物。检测牛血清中的IgM和IgG1抗MPT53表明,在牛自然感染和实验感染牛分枝杆菌后,MPT53具有免疫原性。mpt53的克隆代表了最初基于“定位指数”(LI)测定被定义为结核分枝杆菌和牛分枝杆菌“分泌蛋白”的10种蛋白质中的最后一种的克隆(《普通微生物学杂志》1991年;137:875 - 84)。讨论了对“分泌蛋白”这一术语进行精确定义的必要性。到目前为止,我们观察到表明蛋白质分泌的LI值的出现与相应基因中信号序列的出现完全一致。分枝杆菌中不依赖信号序列的蛋白质分泌可能仅发生在有限数量的蛋白质中,仍有待确定。