Department of Microbiology and Molecular Genetics, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Infect Immun. 2013 Oct;81(10):3742-9. doi: 10.1128/IAI.00441-13. Epub 2013 Jul 29.
Some species of the genus Mycoplasma code for the arginine deiminase pathway (ADI), which enables these bacteria to produce ATP from arginine by the successive reaction of three enzymes: arginine deiminase (ArcA), ornithine carbamoyltransferase (ArcB), and carbamate kinase (ArcC). It so far appears that independently isolated strains of Mycoplasma pneumoniae encode an almost identical truncated version of the ADI pathway in which the proteins ArcA and ArcB have lost their original enzymatic activities due to the deletion of significant regions of these proteins. To study the consequences of a functional ADI pathway, M. pneumoniae M129 was successfully transformed with the cloned functional arcA, arcB, and arcC genes from Mycoplasma fermentans. Enzymatic tests showed that while the M. pneumoniae ArcAB and ArcABC transformants possess functional arginine deiminase, ornithine carbamoyltransferase, and carbamate kinase, they were unable to grow on arginine as the sole energy source. Nevertheless, infection of a lung epithelial cell line, A549, with the M. pneumoniae transformants showed that almost 100% of the infected host cells were nonviable, while most of the lung cells infected with nontransformed M. pneumoniae were viable under the same experimental conditions.
一些支原体属的物种编码精氨酸脱亚氨酶途径 (ADI),该途径使这些细菌能够通过三种酶的连续反应从精氨酸中产生 ATP:精氨酸脱亚氨酶 (ArcA)、鸟氨酸氨甲酰转移酶 (ArcB) 和氨甲酰磷酸激酶 (ArcC)。到目前为止,似乎独立分离的肺炎支原体菌株编码几乎相同的 ADI 途径的截断版本,其中由于这些蛋白质的重要区域缺失,ArcA 和 ArcB 失去了其原始的酶活性。为了研究功能性 ADI 途径的后果,成功地将发酵支原体的克隆功能 arcA、arcB 和 arcC 基因转化为肺炎支原体 M129。酶试验表明,尽管肺炎支原体 ArcAB 和 ArcABC 转化体具有功能性的精氨酸脱亚氨酶、鸟氨酸氨甲酰转移酶和氨甲酰磷酸激酶,但它们无法以精氨酸作为唯一能源生长。然而,用肺炎支原体转化体感染肺上皮细胞系 A549 表明,几乎 100%的感染宿主细胞是不可存活的,而在相同的实验条件下,大多数感染非转化肺炎支原体的肺细胞是存活的。