Baureder Michael, Hederstedt Lars
Microbiology Group, Department of Biology, Lund University, Sweden.
Protein Expr Purif. 2011 Nov;80(1):97-101. doi: 10.1016/j.pep.2011.05.013. Epub 2011 May 27.
Cytochrome b₅₅₈ of the gram-positive bacterium Bacillussubtilis is the membrane anchor subunit of the succinate:quinone oxidoreductase of the citric acid cycle. The cytochrome consists of the SdhC polypeptide (202 residues) and two protoheme IX groups that function in transmembrane electron transfer to menaquinone. The general structure of the cytochrome is known from extensive experimental studies and by comparison to Wolinellasuccinogenes fumarate reductase for which the X-ray crystal structure has been determined. Solution state NMR can potentially be used to identify the quinone binding site(s) and study, e.g. redox-linked, dynamics of cytochrome b₅₅₈. In this work we present an efficient procedure for the isolation of preparative amounts of isotopically labeled B. subtilis cytochrome b₅₅₈ produced in Escherichia coli. We have also evaluated several detergents suitable for NMR for their effectiveness in maintaining the cytochrome solubilized and intact for days at room temperature.
革兰氏阳性细菌枯草芽孢杆菌的细胞色素b₅₅₈是柠檬酸循环中琥珀酸:醌氧化还原酶的膜锚定亚基。该细胞色素由SdhC多肽(202个残基)和两个原血红素IX基团组成,它们在跨膜电子传递至甲基萘醌的过程中发挥作用。通过广泛的实验研究,并与已确定X射线晶体结构的沃氏琥珀酸杆菌延胡索酸还原酶进行比较,该细胞色素的总体结构已为人所知。溶液态核磁共振可用于识别醌结合位点,并研究例如细胞色素b₅₅₈的氧化还原相关动力学。在这项工作中,我们展示了一种从大肠杆菌中制备分离出大量同位素标记的枯草芽孢杆菌细胞色素b₅₅₈的有效方法。我们还评估了几种适用于核磁共振的去污剂,以确定它们在室温下使细胞色素保持溶解和完整状态达数天的有效性。