| Project/Area Number |
08044202
|
|---|
| Research Category |
Grant-in-Aid for international Scientific Research
|
| Allocation Type | Single-year Grants |
|---|
| Section | Joint Research |
|---|
| Research Field |
応用微生物学・応用生物化学
|
|---|
| Research Institution | Faculty of Textile Science, Kyoto Institute of Technology |
|---|
Principal Investigator |
ODA Kohei Kyoto Institute of Technology, Department of Applied Biology, Professor, 繊維学部, 教授 (50081584)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
HIRAGA Kazumi Kyoto Institute of Technology, Department of Applied Biology, Assistant, 繊維学部, 助手 (50252549)
OYAMA Hiroshi Kyoto Institute of Technology, Department of Applied Biology, Lecturer, 繊維学部, 講師 (50221700)
KAY John ウェールズ大学カーディフ校, 分子医生物科学部, 教授
DUNN Ben M フロリダ大学, 医学部, 教授
DUNN B.M. University of Florida College of Medicine, Professor
KAY Jhon University of Wales College of Cardiff, Professor
高橋 砂織 京都工芸繊維大学, 繊維学部, 助教授 (10142184)
DUNN Ben M. フロリダ大学, 医学部, 教授
|
|---|
| Project Period (FY) |
1996 – 1998
|
| Project Status |
Completed (Fiscal Year 1998)
|
| Budget Amount *help |
¥6,700,000 (Direct Cost: ¥6,700,000)
Fiscal Year 1998: ¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1997: ¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥2,300,000 (Direct Cost: ¥2,300,000)
|
|---|
| Keywords | Prokaryote / Pepstatin / Carboxyl proteinase / Acid proteinase / Aspartic proteinase / Catalytic residue (s) / Amino acid sequence / Structure-Function Relationship / カルボキシルプロテアーゼ / ペプスタチン |
|---|
| Research Abstract |
In this study, we aimed to identify the catalytic residues of pepstatin-insensitive carboxyl proteinases from prokaryote cells. We focussed our studies on carboxyl proteinases from Pseudomonas sp. 101 (PCP), Xanthomonas sp. T-22 (XCP). Bacillus coagulans J-4 (J-4), and Bacillus novosp. MN-32 (kumamolysin). The primary structures of them does not have any similarities to those of aspartic proteinases (pepstatin-insensitive carboxyl proteinase) reported so far. Moreover, the well-conserved structure. -Asp*-Thr-Gly-(Asp* : catalytic residue) in the active center of aspartic proteinases was not observed. The following results were obtained.
1. Substrate Specificity and Subsite Structure of Kumamolysin
Substrate specificity of Kumamolysin was investigated by using two sets of synthetic substrates. The subsite structure of Kumamolysin was found to be different with those of aspartic proteinases. These data will be published in J.Biochem.
2. Identification of Catalytic Residues by Using [^<14>C]
… More
Stylene Oxide
In order to identify the catalytic residue(s) of XCP, [^<14>C] stylene oxide was used. It was found that the [^<14>C]stylene oxide was bound to E75 and D110 residues of XCP, respectively. Of them, E75 residue (corresponding to E80 residue of PCP) and its vicinities were conserved in PCP.Based on these data, E80 residue of PCP and E75 residue of XCP were thought to be involved in their catalytic function, as a substrate binding site, respectively.
3. Identification of Catalytic Residues by Using [^<14>C] DCCD
In order to identify the catalytic residue(s) of PCP, chemical modification was carried out by using N.N'-dicyclohexylcafrbodiimide (DCCD) and specific inhibitor. tyrostatin, It was found that [^<14>C] DCCD was bound to D140 and E222 residues of PCP, respectively. Of them, E222 residue (corresponding to E235 residue of XCP) and its vicinities were found out to be conserved in XCP.Furthermore, E222A mutant had no any activity, whereas XE235A (corresponding to E222A for PCP) had proteinase activity. Based on these data. E222 residue of PCP and E235 of XCP were thought to be involved in their catalytic function. probably as a substrate binding site, respectively.
4. Cloning of Carboxyl Proteinase J-4 Gene from Bacillus coagulans
Bacillus coagulans J-4 carboxyl proteinase. designated as J-4. is characterized as alcohol resistant and insensitive to pepstatin. Most of the gene has been cloned, sequenced. After getting the whole gene, we will try to construct a high expression system and determine the catalytic residues by site-directed mutagenesis. Less
|
