Chlumsky L J, Sturgess A W, Nieves E, Jorns M S
Department of Biochemistry, Allegheny University of the Health Sciences, MCP-Hahnemann School of Medicine, Philadelphia, Pennsylvania 19129, USA.
Biochemistry. 1998 Feb 24;37(8):2089-95. doi: 10.1021/bi972705s.
Sarcosine oxidase from Corynebacterium sp. P-1 is a heterotetrameric enzyme (alphabetagammadelta) that contains two noncovalently bound coenzymes (FAD, NAD+) and covalently bound FMN [8alpha-(N3-histidyl)FMN] which is attached to the beta subunit. Chlumsky et al. [(1995) J. Biol. Chem. 270, 18252-18259] tentatively identified His175 as the covalent FMN attachment site in the beta subunit, based on an alignment of the sequence of C. sp. P-1 beta subunit with a highly homologous flavin-containing peptide from another corynebacterial sarcosine oxidase (C. sp. U-96). To test this hypothesis, His175 in the C. sp. P-1 beta subunit was mutated to an alanine. Unexpectedly, the mutant enzyme was found to contain 1 mol of covalently bound flavin and to exhibit catalytic activity similar to wild-type enzyme. Covalent flavin-containing peptides were isolated from wild-type and mutant enzymes and analyzed by electrospray mass spectrometry. The mass observed for the mutant peptide (1152.4 Da) matched that predicted for an FMN-containing hexapeptide, corresponding to residues 173-178 (1152.1 Da). In the mutant, this region (HDAVAW) contains a single histidine (His173) which must be the covalent flavin attachment site. The mass observed for the wild-type peptide (1218.6 Da) matched that predicted for an FMN-containing hexapeptide, also corresponding to residues 173-178 in the beta subunit (1218.2 Da). This region in the wild-type enzyme includes two histidine residues (HDHVAW). Attempts to sequence the wild-type or mutant peptides by automated Edman degradation were unsuccessful. Instead, the peptide sequences were investigated by collisional-activated dissociation (CAD) and tandem mass spectrometry. The CAD mass spectral data with the mutant peptide confirmed the sequence deduced based on the mass of the intact peptide. The CAD mass spectral results with the wild-type peptide showed that FMN was covalently attached to the N-terminal histidine in the hexapeptide, which corresponds to His173 in the beta subunit.
来自棒状杆菌属P-1的肌氨酸氧化酶是一种异源四聚体酶(αβγδ),它含有两个非共价结合的辅酶(FAD、NAD+)和共价结合的FMN [8α-(N3-组氨酰基)FMN],该FMN附着于β亚基。Chlumsky等人[(1995年)《生物化学杂志》270, 18252 - 18259]基于棒状杆菌属P-1β亚基的序列与另一种棒状杆菌肌氨酸氧化酶(棒状杆菌属U-96)的高度同源的含黄素肽段的比对,初步确定His175为β亚基中共价FMN附着位点。为了验证这一假设,将棒状杆菌属P-1β亚基中的His175突变为丙氨酸。出乎意料的是,发现突变酶含有1摩尔共价结合的黄素,并表现出与野生型酶相似的催化活性。从野生型和突变型酶中分离出共价含黄素肽段,并通过电喷雾质谱法进行分析。突变肽段观察到的质量(1152.4 Da)与预测的含FMN六肽的质量相符,对应于173 - 178位残基(1152.1 Da)。在突变体中,该区域(HDAVAW)含有单个组氨酸(His173),它必定是共价黄素附着位点。野生型肽段观察到的质量(1218.6 Da)与预测的含FMN六肽的质量相符,也对应于β亚基中的173 - 178位残基(1218.2 Da)。野生型酶中的该区域包括两个组氨酸残基(HDHVAW)。通过自动Edman降解对野生型或突变型肽段进行测序的尝试均未成功。相反,通过碰撞激活解离(CAD)和串联质谱法对肽段序列进行了研究。突变肽段的CAD质谱数据证实了基于完整肽段质量推导的序列。野生型肽段的CAD质谱结果表明,FMN共价附着于六肽中的N端组氨酸,该组氨酸对应于β亚基中的His173。