Bendjennat M, Blanchard A, Loutfi M, Montagnier L, Bahraoui E
Laboratory of Immunovirology UFR SVT, University of Paul Sabatier, Toulouse, France.
J Bacteriol. 1997 Apr;179(7):2210-20. doi: 10.1128/jb.179.7.2210-2220.1997.
The major nuclease from Mycoplasma penetrans has been purified to homogeneity. The enzyme seems to be present as a membrane-associated precursor of 50 kDa and as a peripheral membrane monomeric polypeptide of 40 kDa that is easily removed by washing of cells with isotonic buffers and in the aqueous phase upon Triton partitioning of Triton X-114-solubilized protein. The 40-kDa nuclease was extracted from M. penetrans cells by Triton X-114 and phase fractionation and was further purified by chromatography on Superdex 75 and chelating Sepharose (Zn2+ form) columns. By gel filtration, the apparent molecular mass was 40 kDa. The purified enzyme exhibits both a nicking activity on superhelical and linear double-stranded DNA and a nuclease activity on RNA and single-stranded DNA. No exonuclease activity was found for this enzyme. This nuclease required both Mg2+ (optimum, 5 mM) and Ca2+ (optimum, 2 mM) for activity and exhibited a pH optimum between pH 7 and 8 for DNase activity. It was inhibited by Zn2+, Mn2+, heparin, sodium dodecyl sulfate, and chelator agents such EDTA and EGTA, but no effect was observed with ATP, 2-mercaptoethanol, N-ethylmaleimide, dithiothreitol, nonionic detergents, phenylmethylsulfonyl fluoride, and iodoacetamide. Nuclease activity was inhibited by diethylpyrocarbonate at both pH 6 and 8 and by pepstatin, suggesting the involvement of a histidine and an aspartate in the active site. When added to human lymphoblast nuclei, the purified M. penetrans endonuclease induced internucleosomal fragmentation of the chomatin into oligonucleosomal fragments. On the basis of this result, and taking into account the fact that M. penetrans has the capacity to invade eucaryotic cells, one can suggest, but not assert, that produced Ca2+/Mg2+-dependent endonuclease may alter the nucleic acid metabolism of host cells by DNA and/or RNA degradation and may act as a potential pathogenic determinant.
穿透支原体的主要核酸酶已被纯化至同质。该酶似乎以50 kDa的膜相关前体形式存在,以及以40 kDa的外周膜单体多肽形式存在,后者在用等渗缓冲液洗涤细胞时很容易去除,并且在用Triton X-114溶解的蛋白质进行Triton分配时存在于水相中。40 kDa的核酸酶通过Triton X-114和相分离从穿透支原体细胞中提取,并通过Superdex 75和螯合琼脂糖(Zn2+形式)柱层析进一步纯化。通过凝胶过滤,其表观分子量为40 kDa。纯化后的酶对超螺旋和线性双链DNA具有切口活性,对RNA和单链DNA具有核酸酶活性。未发现该酶具有外切核酸酶活性。这种核酸酶的活性需要Mg2+(最适浓度为5 mM)和Ca2+(最适浓度为2 mM),并且其DNA酶活性的最适pH值在pH 7至8之间。它受到Zn2+、Mn2+、肝素、十二烷基硫酸钠以及螯合剂如EDTA和EGTA的抑制,但ATP、2-巯基乙醇、N-乙基马来酰亚胺、二硫苏糖醇、非离子去污剂、苯甲基磺酰氟和碘乙酰胺对其没有影响。核酸酶活性在pH 6和8时均受到焦碳酸二乙酯的抑制,并且受到胃蛋白酶抑制剂的抑制,这表明活性位点中涉及一个组氨酸和一个天冬氨酸。当将纯化的穿透支原体内切核酸酶添加到人淋巴母细胞核中时,会诱导染色质的核小体间断裂为寡核小体片段。基于这一结果,并考虑到穿透支原体具有侵入真核细胞的能力,人们可以推测,但不能断言,所产生的Ca2+/Mg2+依赖性内切核酸酶可能通过DNA和/或RNA降解改变宿主细胞的核酸代谢,并可能作为一种潜在的致病决定因素。