Hemmann Jethro L, Saurel Olivier, Ochsner Andrea M, Stodden Barbara K, Kiefer Patrick, Milon Alain, Vorholt Julia A
From the Institute of Microbiology, ETH Zurich, Vladimir-Prelog-Weg 4, 8093 Zurich, Switzerland.
Institute of Pharmacology and Structural Biology, CNRS and Université de Toulouse-Paul Sabatier, 31077 Toulouse, France, and.
J Biol Chem. 2016 Apr 22;291(17):9042-51. doi: 10.1074/jbc.M116.714741. Epub 2016 Feb 19.
Methylobacterium extorquens AM1 uses dedicated cofactors for one-carbon unit conversion. Based on the sequence identities of enzymes and activity determinations, a methanofuran analog was proposed to be involved in formaldehyde oxidation in Alphaproteobacteria. Here, we report the structure of the cofactor, which we termed methylofuran. Using an in vitro enzyme assay and LC-MS, methylofuran was identified in cell extracts and further purified. From the exact mass and MS-MS fragmentation pattern, the structure of the cofactor was determined to consist of a polyglutamic acid side chain linked to a core structure similar to the one present in archaeal methanofuran variants. NMR analyses showed that the core structure contains a furan ring. However, instead of the tyramine moiety that is present in methanofuran cofactors, a tyrosine residue is present in methylofuran, which was further confirmed by MS through the incorporation of a (13)C-labeled precursor. Methylofuran was present as a mixture of different species with varying numbers of glutamic acid residues in the side chain ranging from 12 to 24. Notably, the glutamic acid residues were not solely γ-linked, as is the case for all known methanofurans, but were identified by NMR as a mixture of α- and γ-linked amino acids. Considering the unusual peptide chain, the elucidation of the structure presented here sets the basis for further research on this cofactor, which is probably the largest cofactor known so far.
嗜甲基甲基杆菌AM1利用专用辅因子进行一碳单位转化。基于酶的序列同一性和活性测定,有人提出一种甲呋喃类似物参与α-变形菌中的甲醛氧化。在此,我们报告了这种辅因子的结构,我们将其命名为甲基呋喃。通过体外酶分析和液相色谱-质谱联用,在细胞提取物中鉴定出甲基呋喃并进一步纯化。根据精确质量和质谱-质谱碎片模式,确定该辅因子的结构由连接到与古菌甲呋喃变体中存在的核心结构相似的核心结构上的聚谷氨酸侧链组成。核磁共振分析表明,核心结构包含一个呋喃环。然而,甲基呋喃中存在的是酪氨酸残基,而不是甲呋喃辅因子中存在的酪胺部分,通过掺入(13)C标记的前体,质谱进一步证实了这一点。甲基呋喃以不同物种的混合物形式存在,侧链中谷氨酸残基的数量从12到24不等。值得注意的是,谷氨酸残基并非如所有已知甲呋喃那样仅通过γ连接,核磁共振鉴定其为α-和γ连接氨基酸的混合物。考虑到这种不寻常的肽链,本文对该结构的阐明为进一步研究这种辅因子奠定了基础,它可能是迄今为止已知的最大的辅因子。