Identification of the covalent flavin attachment site in sarcosine oxidase

被引:17
作者
Chlumsky, LJ
Sturgess, AW
Nieves, E
Jorns, MS [1 ]
机构
[1] Allegheny Univ Hlth Sci, MCP, Hahnemann Sch Med, Dept Biochem, Philadelphia, PA 19129 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10461 USA
关键词
D O I
10.1021/bi972705s
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sarcosine oxidase from Corynebacterium sp. P-I is a heterotetrameric enzyme (alpha beta gamma delta), that contains two noncovalently bound coenzymes (FAD, NAD(+)) and covalently bound FMN [8 alpha-(N-3-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-l 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-I 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.
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页码:2089 / 2095
页数:7
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