Institut für Molekulare Mikrobiologie und Biotechnologie, Westfälische Wilhelms-Universität Münster, Münster, Germany.
J Bacteriol. 2014 Feb;196(4):882-93. doi: 10.1128/JB.01265-13. Epub 2013 Dec 6.
In a previous study, the essential role of 3-sulfinopropionyl coenzyme A (3SP-CoA) desulfinase acyl-CoA dehydrogenase (Acd) in Advenella mimigardefordensis strain DPN7(T) (AcdDPN7) during degradation of 3,3'-dithiodipropionic acid (DTDP) was elucidated. DTDP is a sulfur-containing precursor substrate for biosynthesis of polythioesters (PTEs). AcdDPN7 showed high amino acid sequence similarity to acyl-CoA dehydrogenases but was unable to catalyze a dehydrogenation reaction. Hence, it was investigated in the present study whether 3SP-CoA desulfinase activity is an uncommon or a widespread property within the acyl-CoA dehydrogenase superfamily. Therefore, proteins of the acyl-CoA dehydrogenase superfamily from Advenella kashmirensis WT001, Bacillus cereus DSM31, Cupriavidus necator N-1, Escherichia coli BL21, Pseudomonas putida KT2440, Burkholderia xenovorans LB400, Ralstonia eutropha H16, Variovorax paradoxus B4, Variovorax paradoxus S110, and Variovorax paradoxus TBEA6 were expressed in E. coli strains. All purified acyl-CoA dehydrogenases appeared as homotetramers, as revealed by size exclusion chromatography. AcdS110, AcdB4, AcdH16, and AcdKT2440 were able to dehydrogenate isobutyryl-CoA. AcdKT2440 additionally dehydrogenated butyryl-CoA and valeryl-CoA, whereas AcdDSM31 dehydrogenated only butyryl-CoA and valeryl-CoA. No dehydrogenation reactions were observed with propionyl-CoA, isovaleryl-CoA, succinyl-CoA, and glutaryl-CoA for any of the investigated acyl-CoA dehydrogenases. Only AcdTBEA6, AcdN-1, and AcdLB400 desulfinated 3SP-CoA and were thus identified as 3SP-CoA desulfinases within the acyl-CoA dehydrogenase family, although none of these three Acds dehydrogenated any of the tested acyl-CoA thioesters. No appropriate substrates were identified for AcdBL21 and AcdWT001. Spectrophotometric assays provided apparent Km and Vmax values for active substrates and indicated the applicability of phylogenetic analyses to predict the substrate range of uncharacterized acyl-CoA dehydrogenases. Furthermore, C. necator N-1 was found to utilize 3SP as the sole source of carbon and energy.
在之前的研究中,阐明了 3-磺酰丙酰辅酶 A(3SP-CoA)脱磺酰酶酰基辅酶 A 脱氢酶(Acd)在 Advenella mimigardefordensis 菌株 DPN7(T)(AcdDPN7)降解 3,3'-二硫代二丙酸(DTDP)中的重要作用。DTDP 是多硫酯(PTE)生物合成的含硫前体底物。AcdDPN7 与酰基辅酶 A 脱氢酶具有很高的氨基酸序列相似性,但不能催化脱氢反应。因此,本研究探讨了 3SP-CoA 脱磺酰酶活性是否是酰基辅酶 A 脱氢酶超家族中一种不常见或广泛存在的特性。因此,从 Advenella kashmirensis WT001、蜡状芽孢杆菌 DSM31、铜绿假单胞菌 N-1、大肠杆菌 BL21、恶臭假单胞菌 KT2440、伯克霍尔德氏菌 xenovorans LB400、雷氏普罗维登斯菌 H16、鞘氨醇单胞菌 paradoxus B4、鞘氨醇单胞菌 paradoxus S110 和鞘氨醇单胞菌 paradoxus TBEA6 中表达了酰基辅酶 A 脱氢酶超家族的蛋白质。所有纯化的酰基辅酶 A 脱氢酶均通过大小排阻色谱法显示为同源四聚体。AcdS110、AcdB4、AcdH16 和 AcdKT2440 能够使异丁酰辅酶 A 脱氢。AcdKT2440 还能使丁酰辅酶 A 和戊酰辅酶 A 脱氢,而 AcdDSM31 仅能使丁酰辅酶 A 和戊酰辅酶 A 脱氢。对于所有研究的酰基辅酶 A 脱氢酶,都没有观察到丙酰辅酶 A、异戊酰辅酶 A、琥珀酰辅酶 A 和戊二酰辅酶 A 的脱氢反应。只有 AcdTBEA6、AcdN-1 和 AcdLB400 脱磺酰化了 3SP-CoA,因此被鉴定为酰基辅酶 A 脱氢酶家族中的 3SP-CoA 脱磺酰酶,尽管这三种 Acds 都没有使任何测试的酰基辅酶 A 硫酯脱氢。AcdBL21 和 AcdWT001 没有确定合适的底物。分光光度测定法为活性底物提供了表观 Km 和 Vmax 值,并表明系统发育分析可用于预测未表征酰基辅酶 A 脱氢酶的底物范围。此外,还发现 C. necator N-1 可以 3SP 作为唯一的碳源和能源。