Literature DB >> 16751527

Ca2+-dependent maturation of subtilisin from a hyperthermophilic archaeon, Thermococcus kodakaraensis: the propeptide is a potent inhibitor of the mature domain but is not required for its folding.

Marian Pulido1, Kenji Saito, Shun-Ichi Tanaka, Yuichi Koga, Masaaki Morikawa, Kazufumi Takano, Shigenori Kanaya.   

Abstract

Subtilisin from the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1 is a member of the subtilisin family. T. kodakaraensis subtilisin in a proform (T. kodakaraensis pro-subtilisin), as well as its propeptide (T. kodakaraensis propeptide) and mature domain (T. kodakaraensis mat-subtilisin), were independently overproduced in E. coli, purified, and biochemically characterized. T. kodakaraensis pro-subtilisin was inactive in the absence of Ca2+ but was activated upon autoprocessing and degradation of propeptide in the presence of Ca2+ at 80 degrees C. This maturation process was completed within 30 min at 80 degrees C but was bound at an intermediate stage, in which the propeptide is autoprocessed from the mature domain (T. kodakaraensis mat-subtilisin*) but forms an inactive complex with T. kodakaraensis mat-subtilisin*, at lower temperatures. At 80 degrees C, approximately 30% of T. kodakaraensis pro-subtilisin was autoprocessed into T. kodakaraensis propeptide and T. kodakaraensis mat-subtilisin*, and the other 70% was completely degraded to small fragments. Likewise, T. kodakaraensis mat-subtilisin was inactive in the absence of Ca2+ but was activated upon incubation with Ca2+ at 80 degrees C. The kinetic parameters and stability of the resultant activated protein were nearly identical to those of T. kodakaraensis mat-subtilisin*, indicating that T. kodakaraensis mat-subtilisin does not require T. kodakaraensis propeptide for folding. However, only approximately 5% of T. kodakaraensis mat-subtilisin was converted to an active form, and the other part was completely degraded to small fragments. T. kodakaraensis propeptide was shown to be a potent inhibitor of T. kodakaraensis mat-subtilisin* and noncompetitively inhibited its activity with a Ki of 25 +/- 3.0 nM at 20 degrees C. T. kodakaraensis propeptide may be required to prevent the degradation of the T. kodakaraensis mat-subtilisin molecules that are activated later by those that are activated earlier.

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Year:  2006        PMID: 16751527      PMCID: PMC1489632          DOI: 10.1128/AEM.02696-05

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  68 in total

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  11 in total

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Authors:  Shun-ichi Tanaka; Kenji Saito; Hyongi Chon; Hiroyoshi Matsumura; Yuichi Koga; Kazufumi Takano; Shigenori Kanaya
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2006-08-18

2.  Molecular basis for auto- and hetero-catalytic maturation of a thermostable subtilase from thermophilic Bacillus sp. WF146.

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Journal:  J Biol Chem       Date:  2013-10-21       Impact factor: 5.157

3.  Requirement of insertion sequence IS1 for thermal adaptation of Pro-Tk-subtilisin from hyperthermophilic archaeon.

Authors:  Ryo Uehara; Shun-Ichi Tanaka; Kazufumi Takano; Yuichi Koga; Shigenori Kanaya
Journal:  Extremophiles       Date:  2012-09-21       Impact factor: 2.395

4.  Increase in activation rate of Pro-Tk-subtilisin by a single nonpolar-to-polar amino acid substitution at the hydrophobic core of the propeptide domain.

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Journal:  Protein Sci       Date:  2013-10-19       Impact factor: 6.725

5.  In vitro Ca(2+)-dependent maturation of milk-clotting recombinant Epr: minor extracellular protease: from Bacillus licheniformis.

Authors:  José Manuel Ageitos; Juan Andrés Vallejo; Manuel Serrat; Angeles Sánchez-Pérez; Tomás G Villa
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Authors:  Miha Bahun; Marko Šnajder; Dušan Turk; Nataša Poklar Ulrih
Journal:  Appl Environ Microbiol       Date:  2020-08-18       Impact factor: 4.792

7.  Insights into the maturation of hyperthermophilic pyrolysin and the roles of its N-terminal propeptide and long C-terminal extension.

Authors:  Zheng Dai; Heting Fu; Yufeng Zhang; Jing Zeng; Bing Tang; Xiao-Feng Tang
Journal:  Appl Environ Microbiol       Date:  2012-04-13       Impact factor: 4.792

8.  Tobacco phytaspase: Successful expression in a heterologous system.

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9.  Codon optimisation is key for pernisine expression in Escherichia coli.

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10.  Enzymatic activity of a subtilisin homolog, Tk-SP, from Thermococcus kodakarensis in detergents and its ability to degrade the abnormal prion protein.

Authors:  Azumi Hirata; Yuki Hori; Yuichi Koga; Jun Okada; Akikazu Sakudo; Kazuyoshi Ikuta; Shigenori Kanaya; Kazufumi Takano
Journal:  BMC Biotechnol       Date:  2013-02-28       Impact factor: 2.563

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