Minami Masahiko, Kureha Orie, Mori Mari, Kamitsuji Hisatoshi, Suzuki Kazumi, Irie Toshikazu
Department of Environmental Science, The University of Shiga Prefecture, 2500 Hassaka-cho, Hikone, Shiga, 522-8533, Japan.
Appl Microbiol Biotechnol. 2007 Jun;75(3):609-18. doi: 10.1007/s00253-007-0850-y. Epub 2007 Feb 17.
To analyze the transcriptome profile during the initiation of manganese peroxidase (MnP) and lignin peroxidase (LiP) production in Phanerochaete chrysosporium, we constructed long serial analysis of gene expression (LongSAGE) libraries. A total of 13,666 tags (the number of cumulative counted tags) that included 6,945 unique tags (the number of distinct tags) were isolated from the day-3 culture, which just started the enzymes production and was 24 h after veratryl alcohol addition and oxygen-purge into the culture (day-2 culture). A total of 12,402 tags that included 6,396 unique tags were isolated from the day-2 culture, in which the activity of enzymes is not detected. The comparison of the two libraries suggested that 38 genes showed significant (p < or = 0.01) fourfold or greater upregulation; this included the MnP gene (mnp2, mnp3) and LiP H8 gene. On the other hand, 43 genes showed significant (p < or = 0.01) fourfold or greater downregulation. This LongSAGE analysis found many new candidate genes regulating the enzymes production.
为了分析黄孢原毛平革菌中锰过氧化物酶(MnP)和木质素过氧化物酶(LiP)产生起始阶段的转录组概况,我们构建了基因表达的长链序列分析(LongSAGE)文库。从第3天的培养物中分离出总共13,666个标签(累计计数标签的数量),其中包括6,945个独特标签(不同标签的数量),该培养物刚开始产生酶,是在向培养物中添加藜芦醇并进行氧气吹扫后24小时(第2天的培养物)。从第2天的培养物中分离出总共12,402个标签,其中包括6,396个独特标签,在该培养物中未检测到酶活性。两个文库的比较表明,有38个基因显示出显著(p≤0.01)四倍或更高的上调;这包括MnP基因(mnp2、mnp3)和LiP H8基因。另一方面,有43个基因显示出显著(p≤0.01)四倍或更高的下调。这项LongSAGE分析发现了许多调控酶产生的新候选基因。