1989 Fiscal Year Final Research Report Summary
Multi-cellulase components produced by Sporotrichum cellulophilum
| Project/Area Number |
63550725
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
発酵工学
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| Research Institution | Osaka University |
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Principal Investigator |
KINOSHITA Shinichi Osaka Univ., ICBiotech., Assoc. Prof., 工学部, 助教授 (50029253)
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| Project Period (FY) |
1988 – 1989
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| Keywords | Sporotrichum cellulophilum / Cellulase / Monoclonal antibody / Cloning of cellulase gene / Multi-cellulase components / Relatedness of cellulases / DNA sequence of cellulase gene / Amino acid sequence of cellulase |
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| Research Abstract |
Cellulases CII1, CII2, CIII1, CIII2, CIII3, CIV were purified to homogeneity from the crude extract of S. cellulophilum, and sugar moieties of CIII2 and CIV were removed. Monoclonal antibodies against all the cellulases were tried to prepare, but only 4 clones were obtained. The reactivities of monoclonal antibodies against all the cellulases were analyzed by ELISA method. Cellulase CIV was most close to CIII2, more close to CIII1, close to CII1 and CIII3, and hardly related to CII2.
The amino terminus of cellulase CIV was blocked and CIV was hydrolyzed with lysyl endopeptidase. Two fractions were purified by HPLC on 5C_4.300 and amino acid sequences of 22 and 31 residues were determined. From those sequences, 8 DNA probes composing of 14 to 24 bases were synthesized. The RNA of S. cellulophilum was extracted, the cDNA library was prepared. By using probe T (20 mer), positive clones were screened from the library, those were recloned, and hybridized with probe (23 mer), but none of them was not.
In the above method the cDNA was not prepared with good yield. Then we extracted DNA from the cell, and after hydrolyzing it partially with SamIIIA1, the DNA library was prepared. It was screened with probe B.(23 mer), and 4.9 kbp fragment was obtained. After recloning to 400 bp AluI-AluII fragment, its DNA sequence was determined, but any part of the sequence did not correspond with the amino acid sequence. Next by using probe D (29 mer), 500 bp Smal-kpnI and 1050 EcoT22I-Xba1 fragments were isolated, those DNA sequences were determined, regions corresponding to amino acid sequence of 7 and 6 residues were found but the DNA sequences corresponding to other connecting amino acid sequence were not found near the regions. So cellulase gene is not cloned yet.
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