Stabilization of Pseudomonas aeruginosa Cytochrome c551 by Systematic Amino Acid Substitutions Based on the Structure of Thermophilic Hydrogenobacter thermophilus Cytochrome c552

Journal of Biological Chemistry 274 巻 53 号 37533-37537 頁 1999-12-31 発行
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タイトル ( eng )
Stabilization of Pseudomonas aeruginosa Cytochrome c551 by Systematic Amino Acid Substitutions Based on the Structure of Thermophilic Hydrogenobacter thermophilus Cytochrome c552
作成者
Hasegawa Jun
Shimahara Hideto
Mizutani Masayuki
Uchiyama Susumu
Arai Hiroyuki
Ishii Masaharu
Kobayashi Yuji
Ferguson Stuart J.
Igarashi Yasuo
収録物名
Journal of Biological Chemistry
274
53
開始ページ 37533
終了ページ 37537
抄録
A heterologous overexpression system for mesophilic Pseudomonas aeruginosa holocytochrome c551 (PA c551) was established using Escherichia coli as a host organism. Amino acid residues were systematically substituted in three regions of PA c551 with the corresponding residues from thermophilic Hydrogenobacter thermophilus cytochrome c552 (HT c552), which has similar main chain folding to PA c551, but is more stable to heat. Thermodynamic properties of PA c551 with one of three single mutations (Phe-7 to Ala, Phe-34 to Tyr, or Val-78 to Ile) showed that these mutants had increased thermostability compared with that of the wild-type. Ala-7 and Ile-78 may contribute to the thermostability by tighter hydrophobic packing, which is indicated by the three dimensional structure comparison of PA c551 with HT c552. In the Phe-34 to Tyr mutant, the hydroxyl group of the Tyr residue and the guanidyl base of Arg-47 formed a hydrogen bond, which did not exist between the corresponding residues in HT c552. We also found that stability of mutant proteins to denaturation by guanidine hydrochloride correlated with that against the thermal denaturation. These results and others described here suggest that significant stabilization of PA c551 can be achieved through a few amino acid substitutions determined by molecular modeling with reference to the structure of HT c552. The higher stability of HT c552 may in part be attributed to some of these substitutions.
内容記述
This work was supported in part by grants from the Japanese Ministry of Education, Science and Culture.
言語
英語
資源タイプ 学術雑誌論文
出版者
The American Society for Biochemistry and Molecular Biology, Inc.
発行日 1999-12-31
権利情報
This research was originally published in the Journal of Biological Chemistry. Jun Hasegawa, Hideto Shimahara, Masayuki Mizutani, Susumu Uchiyama, Hiroyuki Arai, Masaharu Ishii, Yuji Kobayashi, Stuart J. Ferguson, Yoshihiro Sambongi and Yasuo Igarashi. Stabilization of Pseudomonas aeruginosa Cytochrome c551 by Systematic Amino Acid Substitutions Based on the Structure of Thermophilic Hydrogenobacter thermophilus Cytochrome c552. J. Biol. Chem. 1999; 274(53):37533-37537. © the American Society for Biochemistry and Molecular Biology.
出版タイプ Version of Record(出版社版。早期公開を含む)
アクセス権 オープンアクセス
収録物識別子
[ISSN] 0021-9258
[ISSN] 1083-351X
[DOI] 10.1074/jbc.274.53.37533
[PMID] 10608805
[DOI] https://doi.org/10.1074/jbc.274.53.37533