Xiong Min, Wu Bin, He Huoguang, Li Yang, Wang Xingguo
Faculty of Life Sciences, Hubei University, Wuhan 430062, China.
Wei Sheng Wu Xue Bao. 2011 Jun;51(6):747-55.
Prokaryotes synthesize phosphotidylcholine by using phospholipid N-methylation or phosphatidylcholine synthase pathway or both. To confirm which pathway the soil bacterium Pseudomonas sp. 593 utilizes, we tested its phosphotidylcholine synthesis, cloned the pcs gene encoding phosphatidylcholine synthase, examined Pcs activity, and constructed a pcs mutant.
To clone the pcs gene from Pseudomonas sp. 593 genomic DNA, we firstly aligned amino acid sequences of phosphatidylcholine synthases in different pseudomonas strains reported in databases. Then we designed degenerate primers based on two amino acid segments conserved in sequences of phosphatidylcholine synthases. A partial fragment of the pcs gene was finally amplified from Pseudomonas sp. 593 genomic DNA. The amplified partial fragment was labeled with digoxigenin-dUTP (DIG) as a probe, sub-cloning library of Pseudomonas sp. 593 genomic DNA was prepared and then screened using DIG-labelled probe via in situ colony hybridization. DNA homologous recombination in vivo was preformed to delete pcs gene of Pseudomonas sp. 593. Thin-layer chromatography (TLC) assay was used to analyze total phospholipids, detect phosphotidylcholine content and determine pcs gene activity.
TLC analysis revealed that Pseudomonas sp. 593 growing in the M9 or LB medium with choline was able to synthesize phosphotidylcholine, but wasn't without addition of choline. A 894 bp DNA fragment coded a protein with phosphatidylcholine synthase activity was cloned from Pseudomonas sp. 593. The pcs mutant obtained from in vivo mutagenesis was unable to form phosphotidylcholine, no matter choline was presented in the medium or not.
Phosphatidylcholine synthase pathway is a sole way for phosphotidylcholine synthesis in soil bacterium Pseudomonas sp. 593 or other Pseudomonas strains.
原核生物通过磷脂N - 甲基化途径或磷脂酰胆碱合酶途径或两者兼用来合成磷脂酰胆碱。为了确定土壤细菌假单胞菌属593利用的是哪种途径,我们测试了其磷脂酰胆碱的合成,克隆了编码磷脂酰胆碱合酶的pcs基因,检测了Pcs活性,并构建了一个pcs突变体。
为了从假单胞菌属593基因组DNA中克隆pcs基因,我们首先比对了数据库中报道的不同假单胞菌菌株中磷脂酰胆碱合酶的氨基酸序列。然后根据磷脂酰胆碱合酶序列中两个保守的氨基酸片段设计了简并引物。最终从假单胞菌属593基因组DNA中扩增出pcs基因的一个部分片段。将扩增的部分片段用地高辛 - dUTP(DIG)标记作为探针,制备假单胞菌属593基因组DNA的亚克隆文库,然后通过原位菌落杂交用DIG标记的探针进行筛选。通过体内DNA同源重组删除假单胞菌属593的pcs基因。采用薄层色谱(TLC)分析总磷脂,检测磷脂酰胆碱含量并确定pcs基因活性。
TLC分析表明,在含有胆碱的M9或LB培养基中生长的假单胞菌属593能够合成磷脂酰胆碱,但在不添加胆碱的情况下则不能。从假单胞菌属593中克隆出一个894 bp的DNA片段,其编码的蛋白质具有磷脂酰胆碱合酶活性。通过体内诱变获得的pcs突变体无论培养基中是否存在胆碱都无法形成磷脂酰胆碱。
磷脂酰胆碱合酶途径是土壤细菌假单胞菌属593或其他假单胞菌菌株合成磷脂酰胆碱的唯一途径。