Mercado Gabriela, Tello Mario, Marín Macarena, Monasterio Octavio, Lagos Rosalba
Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile.
J Bacteriol. 2008 Aug;190(15):5464-71. doi: 10.1128/JB.00351-08. Epub 2008 May 23.
Microcin E492 is a channel-forming bacteriocin that is found in two forms, namely, a posttranslationally modified form obtained by the covalent linkage of salmochelin-like molecules to serine 84 and an unmodified form. The production of modified microcin E492 requires the synthesis of enterochelin, which is subsequently glycosylated by MceC and converted into salmochelin. mceC mutants produced inactive microcin E492, and this phenotype was reversed either by complementation with iroB from Salmonella enterica or by the addition of exogenous salmochelin. Cyclic salmochelin uptake by Escherichia coli occurred mainly through the outer membrane catecholate siderophore receptor Fiu. The production of inactive microcin E492 by mutants in entB and entC was reverted by the addition of the end product of the respective mutated pathway (2,3-dihydroxybenzoic acid and enterochelin/salmochelin, respectively), while mutants in entF did not produce active microcin E492 in the presence of enterochelin or salmochelin. The EntF adenylation domain was the only domain required for this microcin E492 maturation step. Inactivation of the enzymatic activity of this domain by site-directed mutagenesis did not prevent the synthesis of active microcin E492 in the presence of salmochelin, indicating that the adenylation activity is not essential for the function of EntF at this stage of microcin E492 maturation.
微菌素E492是一种形成通道的细菌素,它有两种形式,即通过类沙门菌素样分子与丝氨酸84共价连接获得的翻译后修饰形式和未修饰形式。修饰后的微菌素E492的产生需要肠螯合素的合成,随后肠螯合素被MceC糖基化并转化为沙门菌素。mceC突变体产生无活性的微菌素E492,通过用肠炎沙门氏菌的iroB进行互补或添加外源性沙门菌素可逆转这种表型。大肠杆菌对环状沙门菌素的摄取主要通过外膜儿茶酚铁载体受体Fiu进行。entB和entC突变体产生的无活性微菌素E492通过添加各自突变途径的终产物(分别为2,3-二羟基苯甲酸和肠螯合素/沙门菌素)而恢复活性,而entF突变体在存在肠螯合素或沙门菌素的情况下不产生活性微菌素E492。EntF腺苷化结构域是微菌素E492成熟步骤所需的唯一结构域。通过定点诱变使该结构域的酶活性失活,在存在沙门菌素的情况下并不妨碍活性微菌素E492的合成,这表明在微菌素E492成熟的这个阶段,腺苷化活性对EntF的功能不是必需的。