Cumulative stabilizing effects of glycine to alanine substitutions in Bacillus subtilis neutral protease

Immaculada Margarit, Susanna Camagnoli, Francesco Frigerio, Guido Grandi, Vincenzo De Filippis, Angelo Fontana

Research output: Contribution to journalArticle

Abstract

Oligonucleotide-directed mutagenesis has been used to replace glycine residues by alanine in neutral protease from Bacillus subtilis. One Gly to Ala substitution (G147A) was located in a helical region of the protein, while the other (G189A) was in a loop. The effects of mutational substitutions on the functional, conformational and stability properties of the enzyme have been investigated using enzymatic assays and spectroscopic measurements. Single substitutions of both G1y147 and Gly189 with Ala residues affect the enzyme kinetic properties using synthetic peptides as substrates. When Gly replacements were concurrently introduced at both positions, the kinetic characteristics of the double mutant were roughly intermediate between those of the two single mutants, and similar to those of the wild-type protease. Both mutants G147A and G189A were found to be more stable towards irreversible thermal inactivation/unfolding than the wild-type species. Moreover, the stabilizing effect of the Gly to Ala substitution was roughly additive in the double mutant G147A/G189A, which shows a 3.2°C increase in Tm with respect to the wild-type protein. These findings indicate that the Gly to Ala substitution can be used as a strategy to stabilize globular proteins. The possible mechanisms of protein stabilization are also discussed.

Original languageEnglish
Pages (from-to)543-550
Number of pages8
JournalProtein Engineering, Design and Selection
Volume5
Issue number6
DOIs
Publication statusPublished - Sep 1992

Fingerprint

Bacilli
Alanine
Glycine
Amino acids
Substitution reactions
Proteins
Enzyme Stability
Enzyme Assays
Site-Directed Mutagenesis
Enzyme kinetics
Mutagenesis
Oligonucleotides
Peptide Hydrolases
Hot Temperature
Peptides
Assays
Enzymes
Stabilization
bacillolysin
Substrates

Keywords

  • Neutral protease
  • Protein engineering
  • Protein stability
  • Proteolytic enzymes
  • Site-directed mutagenesis

ASJC Scopus subject areas

  • Pharmacology
  • Neuroscience(all)
  • Immunology and Microbiology(all)
  • Molecular Biology
  • Bioengineering
  • Biotechnology
  • Biochemistry

Cite this

Cumulative stabilizing effects of glycine to alanine substitutions in Bacillus subtilis neutral protease. / Margarit, Immaculada; Camagnoli, Susanna; Frigerio, Francesco; Grandi, Guido; Filippis, Vincenzo De; Fontana, Angelo.

In: Protein Engineering, Design and Selection, Vol. 5, No. 6, 09.1992, p. 543-550.

Research output: Contribution to journalArticle

Margarit, Immaculada ; Camagnoli, Susanna ; Frigerio, Francesco ; Grandi, Guido ; Filippis, Vincenzo De ; Fontana, Angelo. / Cumulative stabilizing effects of glycine to alanine substitutions in Bacillus subtilis neutral protease. In: Protein Engineering, Design and Selection. 1992 ; Vol. 5, No. 6. pp. 543-550.
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