Lewin Anna, Hederstedt Lars
Department of Cell and Organism Biology, Lund University, Sölvegatan 35, SE 22362 Lund, Sweden.
FEBS Lett. 2008 Apr 16;582(9):1330-4. doi: 10.1016/j.febslet.2008.03.015. Epub 2008 Mar 20.
Bacillus subtilis heme A synthase is a membrane protein with 8 transmembrane segments. By using a two-step mutagenesis approach we have generated and selected a fully functional enzyme protein variant with a seven residue internal deletion. The biochemical properties of the shortened variant are similar to those of the normal enzyme. This could indicate that residue H209 in the mutant protein substitutes for the missing H216 as an axial ligand to the heme iron. Our results provide insight in routes of membrane protein evolution and the structure of heme A synthases.
枯草芽孢杆菌血红素A合酶是一种具有8个跨膜区段的膜蛋白。通过两步诱变方法,我们生成并筛选出了一种具有7个残基内部缺失的全功能酶蛋白变体。缩短后的变体的生化特性与正常酶相似。这可能表明突变蛋白中的H209残基替代了缺失的H216,作为血红素铁的轴向配体。我们的结果为膜蛋白进化途径和血红素A合酶的结构提供了见解。