Adrian Lorenz, Rahnenführer Jan, Gobom Johan, Hölscher Tina
Fachgebiet Technische Biochemie, Institut für Biotechnologie, Technische Universität Berlin, 13353 Berlin, Germany.
Appl Environ Microbiol. 2007 Dec;73(23):7717-24. doi: 10.1128/AEM.01649-07. Epub 2007 Oct 12.
A chlorobenzene reductive dehalogenase of the anaerobic dehalorespiring bacterium Dehalococcoides sp. strain CBDB1 was identified. Due to poor biomass yields, standard protein isolation procedures were not applicable. Therefore, cell extracts from cultures grown on trichlorobenzenes were separated by native polyacrylamide gel electrophoresis and analyzed directly for chlorobenzene reductive dehalogenase activity within gel fragments. Activity was found in a single band, even though electrophoretic separation was performed under aerobic conditions. Matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) and nano-liquid chromatography-MALDI MS analysis of silver-stained replicas of the active band on native polyacrylamide gels identified a protein product of the cbdbA84 gene, now called cbrA. The cbdbA84 gene is one of 32 reductive dehalogenase homologous genes present in the genome of strain CBDB1. The chlorobenzene reductive dehalogenase identified in our study represents a member of the family of corrinoid/iron-sulfur cluster-containing reductive dehalogenases. No orthologs of cbdbA84 were found in the completely sequenced genomes of Dehalococcoides sp. strains 195 and BAV1 nor among the genes amplified from Dehalococcoides sp. strain FL2 or mixed cultures containing Dehalococcoides. Another dehalogenase homologue (cbdbA80) was expressed in cultures that contained 1,2,4-trichlorobenzene, but its role is unclear. Other highly expressed proteins identified with our approach included the major subunit of a protein annotated as formate dehydrogenase, transporter subunits, and a putative S-layer protein.
已鉴定出厌氧脱卤呼吸细菌脱卤球菌属菌株CBDB1的一种氯苯还原脱卤酶。由于生物量产量较低,标准的蛋白质分离程序并不适用。因此,将在三氯苯上生长的培养物的细胞提取物通过非变性聚丙烯酰胺凝胶电泳进行分离,并直接分析凝胶片段中的氯苯还原脱卤酶活性。尽管电泳分离是在有氧条件下进行的,但在一条单一的条带中发现了活性。对非变性聚丙烯酰胺凝胶上活性条带的银染复制品进行基质辅助激光解吸电离质谱(MALDI MS)和纳升液相色谱 - MALDI MS分析,鉴定出cbdbA84基因的一种蛋白质产物,现在称为cbrA。cbdbA84基因是菌株CBDB1基因组中存在的32个还原脱卤酶同源基因之一。在我们的研究中鉴定出的氯苯还原脱卤酶代表了含类咕啉/铁硫簇的还原脱卤酶家族的一个成员。在脱卤球菌属菌株195和BAV1的全序列基因组中,以及从脱卤球菌属菌株FL2或含有脱卤球菌属的混合培养物中扩增的基因中,均未发现cbdbA84的直系同源物。另一种脱卤酶同源物(cbdbA80)在含有1,2,4 - 三氯苯的培养物中表达,但其作用尚不清楚。用我们的方法鉴定出的其他高表达蛋白包括一种注释为甲酸脱氢酶的主要亚基、转运蛋白亚基和一种假定的S层蛋白。