| Literature DB >> 26454877 |
Ryo Nasuno1, Saeka Hirase1, Saki Norifune1, Daisuke Watanabe1, Hiroshi Takagi2.
Abstract
Previously, N-Acetyltransferase Mpr1 was suggested to be involved in a novel pathway of L-arginine biosynthesis in yeast. Our recent crystallographic analysis demonstrated that the overall structure of Mpr1 is a typical folding among proteins in the Gcn5-related N-acetyltransferase superfamily, and also provided clues to the design of mutations for improvement of the enzymatic functions. Here, we constructed new stable variants, Asn203Lys- and Asn203Arg-Mpr1, which exhibited 2.4-fold and 2.2-fold longer activity half-lives than wild-type Mpr1, respectively, by structure-based molecular design. The replacement of Asn203 with a basic amino acid was suggested to stabilize α-helix 2, which is important for the Mpr1 structure, probably by neutralizing its dipole. In addition, the combination of two amino acid substitutions at positions 65 and 203 in Mpr1, Phe65Leu, which was previously isolated by the screening from PCR random mutagenesis library of MPR1, and Asn203Lys or Asn203Arg, led to further stabilization of Mpr1. Our growth assay suggests that overexpression of the stable Mpr1 variants increase L-arginine synthesis in yeast cells. Our finding is the first report on the rational engineering of Mpr1 for thermostabilization and could be useful in the construction of new yeast strains with higher L-arginine synthetic activity and also improved fermentation ability.Entities:
Keywords: N-acetyltransferase Mpr1; l-arginine biosynthesis; structure-based molecular design; thermostability; yeast
Mesh:
Substances:
Year: 2015 PMID: 26454877 PMCID: PMC4892782 DOI: 10.1093/jb/mvv101
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387