Substrate Specificity Analysis of Microbial Transglutaminase Using Proteinaceous Protease Inhibitors As Natural Model Substrates

• Published in: Journal of biochemistry (Tokyo) Vol. 128; no. 3; pp. 415 - 425
• Main Authors: Taguchi, Seiichi, Nishihama, Kei-ichiro, Igi, Keiko, Ito, Kotaro, Taira, Hiroko, Motoki, Masao, Momose, Haruo
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01-09-2000
• Subjects: amine-donor; Amino Acid Sequence; Animals; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Base Sequence; Chromatography; Cross-Linking Reagents; DNA Primers; ELISA-based assay; Enzyme-Linked Immunosorbent Assay; Genetic Vectors; Guinea Pigs; Liver - enzymology; microbial transgulataminase; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Oxidation-Reduction; Polymerase Chain Reaction; Rabbits; Recombinant Proteins; Sequence Alignment; site-specific mutagenesis; Streptomyces - enzymology; Streptomyces protease inhibitor; Structure-Activity Relationship; Substrate Specificity; Transglutaminases - isolation & purification; Transglutaminases - metabolism; Trypsin Inhibitors - genetics; Trypsin Inhibitors - metabolism
• ISSN: 0021-924X
• DOI: 10.1093/oxfordjournals.jbchem.a022769

The substrate specificity of microbial transglutaminase (MTG) from Streptomyces mobaraensis (formerly categorized Streptoverticillium) was studied using a Streptomyces proteinaceous protease inhibitor, STI2, as a model amine-donor substrate. Chemical modification and mutational analysis to address the substrate requirements for MTG were carried out around the putative reactive site region of STI2 on the basis of the highly refined tertiary structure and the solvent accessibility index of Streptomyces subtilisin inhibitor, SSI, a homolog of STI2. The results suggest that the PI reactive center site (position 70 of STI2) for protease subtilisin BPN' or trypsin may be the prime Lys residue that can be recognized by MTG, when succinylated β-casein was used as a partner Gin-substrate. It is characteristic in that the same primary enzyme contact region of STI2 is shared by both enzymes, MTG and proteases. For quantitative analysis of the TG reaction, we established an ELISA-based monitoring assay system using an anti-SSI polyclonal antibody highly cross-reactive with STI2. Site-specific STI2 mutants were prepared by an Escherichia coli expression-secretion vector system and subjected to the assay system. We reached several conclusions concerning the nature of the flanking amino acid residues affecting the MTG reactivity of the substrate Lys residue: (i) site-specific mutations from Asn to Lys or Arg at position 69 preceding the amine-donor 70Lys, led to enhanced substrate reactivity; (ii) amino acid replacement at 67Ile with Ser led to higher substrate reactivity, (iii) additive effects were obtained by a combination of the positive mutations at positions 67 and 69 as described above, and (iv) Gly at position 65 might be essential for MTG reaction. Moreover, the substrate specificity of guinea pig liver tissue transglutaminase (GTG) was compared with that of MTG using STI2 and its mutants. In contrast to MTG, replacement of Gly by Asp at position 65 was the most favorable for substrate reactivity. Also, 70Lys appeared not to be a prime amine-donor site for GTG-mediated cross-linking, suggesting a difference in substrate recognition between MTG and GTG