MOKUZAI HOZON (Wood Protection)
Online ISSN : 1884-0116
Print ISSN : 0287-9255
ISSN-L : 0287-9255
Volume 34, Issue 6
Displaying 1-7 of 7 articles from this issue
Commentation
Original Article
  • Haruko SAKAI
    2008 Volume 34 Issue 6 Pages 261-268
    Published: 2008
    Released on J-STAGE: December 17, 2011
    JOURNAL FREE ACCESS
    Effectiveness of surface coating with Kakishibu (tannin of Japanese persimmon, Diospyros kaki Thunb.) and the improved ones against decay fungi was tested.
    The test was carried out as described in JIS K 1571: 2004. Wood specimens used were sugi (Cryptomeria japonica D. Don) sapwood. Mass losses of specimens coated with Kakishibu, not leached and subjected by Fomitopsis palustris - FFPRI 0507 and Trametes versicolor - FFPRI 1030, were more than 14% and 8%, respectively. Hyphae of F. palustris entered to the inside of the specimens from cracks of the film of tannin, and hyphae of T. versicolor passed through the film.
    However, the both mass losses became less than 4% when the Kakishibu adding glutaraldehyde and copper sulfate was used for surface coating at two times, though leaching treatment was carried out. By these results, it was thought that aldehyde and copper improved water- and fungal resistance of Kakishibu, respectively.
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  • Makoto YOSHIDA, Yuji NAKADA, Satoshi KANEKO, Kiyoharu FUKUDA
    2008 Volume 34 Issue 6 Pages 269-280
    Published: 2008
    Released on J-STAGE: December 17, 2011
    JOURNAL FREE ACCESS
    To identify the genes encoding the proteins involved in cellulose degradation by the saprogenic basidiomycete Coprinus cinereus, differential display (DD) analysis based on Annealing Control Primer (ACP) system was carried out. Total RNAs were extracted from the mycelia of C. cinereus grown on the medium containing glucose or cellulose as the sole carbon source and then RT-PCR using ACP was performed in order to compare the amplification patterns of PCR products. As a result of DD analysis using 20 kinds of primer pairs, 10 kinds of cellulose culture-specific bands were detected. To confirm the transcript levels of the target genes, the specific primer to the nucleotide sequence of each band was prepared and RT-PCR analysis with the primers was carried out. The expression levels of the genes in the cellulose culture were higher than those in the glucose culture. In the database analysis using the deduced amino acid sequence, it was found that the genes encode various proteins such as not only the polysaccharide-degrading enzyme and the protein involved in carbohydrate metabolism but also cytochrome P450, retrotranspozon-relating protein and G protein-coupled receptor.
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