Abstract
The primary structures of the C and D subunits of sarcosine oxidase from Corynebacterium sp. U-96 were determined by sequencing the peptide fragments derived from their enzymatic digestions. The C and D subunits were shown to be composed of 199 and 92 residues, respectively. Each amino acid sequence showed a high homology with the sequence of the corresponding subunit from Corynebacterium sp. P-1. However, there were some differences between these two species, that is, four N-terminal residues were truncated in the C subunit, but six C-terminal residues were truncated in the D subunit. The D subunit contained three cysteine residues, but no disulfide bonds are in the subunit. Overall sequences of both subunit showed no homology with any other protein in the data base.
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Mukouyama, E.B., Tatemukai, S., Morioka, K. et al. Determination of Amino Acid Sequences of Two Subunits in Sarcosine Oxidase from Corynebacterium sp. U-96. J Protein Chem 18, 747–752 (1999). https://doi.org/10.1023/A:1020625400518
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DOI: https://doi.org/10.1023/A:1020625400518