Jurkowitz Marianne S, Patel Aalapi, Wu Lai-Chu, Krautwater Annalise, Pfeiffer Douglas R, Bell Charles E
Department of Molecular and Cellular Biochemistry, The Ohio State University, Columbus, OH 43210, USA.
Department of Molecular and Cellular Biochemistry, The Ohio State University, Columbus, OH 43210, USA.
Biochim Biophys Acta. 2015 Feb;1848(2):742-51. doi: 10.1016/j.bbamem.2014.11.011. Epub 2014 Nov 16.
Lysoplasmalogenase catalyzes hydrolytic cleavage of the vinyl-ether bond of lysoplasmalogen to yield fatty aldehyde and glycerophospho-ethanolamine or glycerophospho-choline. We recently purified lysoplasmalogenase from rat liver microsomes and identified the protein as TMEM86B, an integral membrane protein that is a member of the YhhN family found in numerous species of eukaryotes and bacteria. To test the hypothesis that bacterial YhhN proteins also function as lysoplasmalogenase enzymes, we cloned the Lpg1991 gene of Legionella pneumophila, which encodes a 216 amino acid YhhN protein (LpYhhN), and expressed it in Escherichia coli as a C-terminal-GFP-His8-fusion. Membranes were solubilized and the fusion protein was purified by nickel-affinity chromatography, cleaved with Tobacco Etch Virus protease, and subjected to a reverse nickel column to purify the un-tagged LpYhhN. Both the fusion protein and un-tagged LpYhhN exhibit robust lysoplasmalogenase activity, cleaving the vinyl-ether bond of lysoplasmalogen with a Vmax of 12 µmol/min/mg protein and a Km of 45 μM. LpYhhN has no activity on diradyl plasmalogen, 1-alkenyl-glycerol, and monoacylglycerophospho-ethanolamine or monoacylglycerophospho-choline; the pH optimum is 6.5-7.0. These properties are very similar to mammalian TMEM86B. Sequence analysis suggests that YhhN proteins contain eight transmembrane helices, an N-in/C-in topology, and about 5 highly conserved amino acid residues that may form an active site. This work is the first to demonstrate a function for a bacterial YhhN protein, as a vinyl ether bond hydrolase specific for lysoplasmalogen. Since L. pneumophila does not contain endogenous plasmalogens, we hypothesize that LpYhhN may serve to protect the bacterium from lysis by lysoplasmalogen derived from plasmalogens of the host.
溶血缩醛磷脂酶催化溶血缩醛磷脂的乙烯基醚键发生水解断裂,生成脂肪醛和甘油磷酸乙醇胺或甘油磷酸胆碱。我们最近从大鼠肝脏微粒体中纯化了溶血缩醛磷脂酶,并鉴定该蛋白为TMEM86B,它是一种整合膜蛋白,属于在众多真核生物和细菌物种中发现的YhhN家族成员。为了验证细菌YhhN蛋白也具有溶血缩醛磷脂酶功能这一假说,我们克隆了嗜肺军团菌的Lpg1991基因,该基因编码一种216个氨基酸的YhhN蛋白(LpYhhN),并将其作为C端-GFP-His8融合蛋白在大肠杆菌中表达。对细胞膜进行增溶处理,通过镍亲和层析纯化融合蛋白,用烟草蚀纹病毒蛋白酶进行切割,然后通过反向镍柱纯化未标记的LpYhhN。融合蛋白和未标记的LpYhhN均表现出强大的溶血缩醛磷脂酶活性,以12 μmol/分钟/毫克蛋白的Vmax和45 μM的Km切割溶血缩醛磷脂的乙烯基醚键。LpYhhN对二烯基缩醛磷脂、1-链烯基甘油以及单酰甘油磷酸乙醇胺或单酰甘油磷酸胆碱均无活性;最适pH为6.5 - 7.0。这些特性与哺乳动物的TMEM86B非常相似。序列分析表明,YhhN蛋白包含8个跨膜螺旋,具有N端向内/C端向内的拓扑结构,以及约5个高度保守的氨基酸残基,这些残基可能形成一个活性位点。这项工作首次证明了细菌YhhN蛋白作为一种对溶血缩醛磷脂具有特异性的乙烯基醚键水解酶的功能。由于嗜肺军团菌不含有内源性缩醛磷脂,我们推测LpYhhN可能有助于保护该细菌免受源自宿主缩醛磷脂的溶血缩醛磷脂导致的裂解。