Molecular characterization of a prolyl endopeptidase from a feather-degrading thermophile Meiothermus ruber H328

• Published in: Journal of biochemistry (Tokyo) Vol. 168; no. 5; pp. 499 - 508
• Main Authors: Yamamoto, Fumi, Morisaka, Hironobu, Ueda, Mitsuyoshi, Watanabe, Kunihiko
• Format: Journal Article
• Language: English
• Published: England 01.11.2020
• Subjects: Amino Acid Sequence; Animals; Bacteria - enzymology; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Catalysis; Chickens; Feathers - metabolism; Feathers - microbiology; Prolyl Oligopeptidases - genetics; Prolyl Oligopeptidases - metabolism; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; Sequence Homology; Substrate Specificity; prolyl oligopeptidase; serine protease; peptidase; Meiothermus ruber; prolyl endopeptidase
• ISSN: 0021-924X; 1756-2651
• DOI: 10.1093/jb/mvaa069

Prolyl endopeptidase from an aerobic and Gram-negative thermophile Meiothermus ruber H328 (MrPEP) was purified in native and recombinant forms, but both preparations had comparable characteristics. Production of the native MrPEP was increased 10-fold by adding intact chicken feathers. The gene for MrPEP (mrH_2860) was cloned from the genome of strain H328 and found to have no signal sequence at the N-terminus. MrPEP is composed of two major domains: the β-propeller domain and the peptidase domain with a typical active site motif and catalytic triad. Based on extensive investigations with different types of peptide substrates and FRETS-25Xaa libraries, MrPEP showed strict preferences for Pro residue at the P1 position but broader preferences at the P2 and P3 positions in substrate specificity with stronger affinity for residues at the P3 position of substrate peptides that are longer than four residues in length. In conclusion, the molecular characterization of MrPEP resembles its animal counterparts more closely than bacterial counterparts in function and structure.