Safinowski Michael, Meckenstock Rainer U
Zentrum für Angewandte Geowissenschaften, Eberhard-Karls Universität Tübingen, Wilhelmstr. 56, D-72076 Tübingen, Germany.
FEMS Microbiol Lett. 2004 Nov 1;240(1):99-104. doi: 10.1016/j.femsle.2004.09.014.
The upper pathway of anaerobic degradation of 2-methylnaphthalene was studied with a sulphate-reducing enrichment culture, which is able to grow with naphthalene or 2-methylnaphthalene as sole carbon source and electron donor. Anaerobic degradation of 2-methylnaphthalene is initiated by an addition of fumarate to the methyl-group producing the first intermediate, naphthyl-2-methyl-succinate. In a subsequent beta-oxidation of the original methyl atom, the central metabolite 2-naphthoic acid is generated. In the following pathway, the aromatic ring system is reduced, cleaved, and finally oxidised to CO(2). Here, we present two new enzymatic reactions of the 2-methylnaphthalene degradation pathway that were measured in crude cell extracts. All metabolites were identified with HPLC by co-elution with synthesised reference substances. The first enzyme, succinyl-CoA:naphthyl-2-methyl-succinate CoA-transferase, catalyses the activation of naphthyl-2-methyl-succinic acid to the corresponding CoA ester. The average specific activity of this enzyme was 19.6 nmol x min(-1) x mg of protein(-1). The CoA-transfer was not inhibited by sodium borohydride and only partially by hydroxylamine, indicating that this enzyme belongs to the family III of CoA-transferases like the corresponding enzyme in the anaerobic toluene degradation pathway. The product of this CoA-transfer reaction, naphthyl-2-methyl-succinyl-CoA is then oxidised in a reaction to naphthyl-2-methylene-succinyl-CoA by the enzyme naphthyl-2-methyl-succinyl-CoA dehydrogenase. The specific activity of this enzyme was 0.115 nmol x min(-1) x mg of protein(-1). The enzymatic activity could only be detected using phenazine methosulphate as electron acceptor. No activity was observed with natural electron acceptors such as nicotinamide adenine dinucleotide or flavin adenine dinucleotide. The two novel reactions presented here demonstrate that the original methyl-group of 2-methylnaphthalene is oxidised to the carboxyl group of 2-naphthoic acid in the upper part of the anaerobic degradation pathway.
利用一种硫酸盐还原富集培养物研究了2-甲基萘的厌氧降解上途径,该培养物能够以萘或2-甲基萘作为唯一碳源和电子供体生长。2-甲基萘的厌氧降解通过向甲基添加富马酸酯引发,生成第一个中间体萘基-2-甲基琥珀酸酯。在原始甲基原子随后的β-氧化过程中,生成中心代谢物2-萘甲酸。在接下来的途径中,芳香环系统被还原、裂解,最终氧化为CO₂。在此,我们展示了在粗细胞提取物中测得的2-甲基萘降解途径的两个新酶促反应。所有代谢物通过与合成参考物质共洗脱,用高效液相色谱法进行鉴定。第一种酶,琥珀酰辅酶A:萘基-2-甲基琥珀酸辅酶A转移酶,催化萘基-2-甲基琥珀酸活化生成相应的辅酶A酯。该酶的平均比活性为19.6 nmol·min⁻¹·mg蛋白质⁻¹。辅酶A转移不受硼氢化钠抑制,仅部分受羟胺抑制,表明该酶属于辅酶A转移酶家族III,类似于厌氧甲苯降解途径中的相应酶。该辅酶A转移反应的产物萘基-2-甲基琥珀酰辅酶A随后被萘基-2-甲基琥珀酰辅酶A脱氢酶氧化为萘基-2-亚甲基琥珀酰辅酶A。该酶的比活性为0.115 nmol·min⁻¹·mg蛋白质⁻¹。该酶活性仅在使用吩嗪硫酸甲酯作为电子受体时才能检测到。使用烟酰胺腺嘌呤二核苷酸或黄素腺嘌呤二核苷酸等天然电子受体未观察到活性。这里展示的两个新反应表明,在厌氧降解途径的上部,2-甲基萘的原始甲基被氧化为2-萘甲酸的羧基。