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首页> 外文期刊>酒類総合研究所報告 >Transcriptional analysis of genes for energy catabolism and hydrolytic enzymes in the filamentous fungus Aspergillus oryzae using cDNA microarrays and expressed sequence tags
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Transcriptional analysis of genes for energy catabolism and hydrolytic enzymes in the filamentous fungus Aspergillus oryzae using cDNA microarrays and expressed sequence tags

机译:利用cDNA芯片和表达序列标签对丝状真菌米曲霉中能量分解代谢和水解酶基因的转录分析。

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摘要

Aspergillus oryzae is a fungus used extensively in the fermentation industry. We constructed cDNA microarrays comprising 2,070 highly expressed cDNAs selected from the ~6,000 non-redundant expressed se­quence tags (ESTs) in the A. oryzae EST database . Using the cDNA microarrays, we analyzed the gene expression profiles of A. oryzae cells grown under the glucose-rich (AC) and glucose-depleted (AN) liquid culture conditions used during the construction of the EST database. The sets of genes identified by the cDNA microarray as highly expressed under each culture condition agreed well with the highly redundant ESTs obtained under the same conditions. In particular, transcription levels of most catabolic genes of the glycolytic pathway (EMP) and tricarboxylic acid (TCA) cycle were higher under AC than AN conditions, suggesting that A. oryzae uses both EMP and TCA for glucose metabolism under AC conditions. We further studied the expression of genes encoding hydrolytic enzymes and enzymes involved in energy catabolism by using three industrial solid-phase biomass media, including wheat-bran. The wheat-bran culture gave the richest gene expression profile of hydrolytic enzymes and the lowest expression levels of catabolic genes (EMP, TCA) among the three media tested. The low expression levels of catabolic genes in the wheat-bran culture may release catabolite repression, consequently leading to the rich expression profiles of the hydrolytic enzymes.
机译:米曲霉是在​​发酵工业中广泛使用的真菌。我们构建了cDNA微阵列,包括从米曲霉EST数据库中的6,000个非冗余表达的序列标签(EST)中选择的2,070个高表达cDNA。使用cDNA微阵列,我们分析了在建立EST数据库期间使用的富含葡萄糖(AC)和缺乏葡萄糖(AN)的液体培养条件下生长的米曲霉细胞的基因表达谱。由cDNA微阵列鉴定为在每种培养条件下均高度表达的基因组与在相同条件下获得的高度冗余的EST很好地吻合。特别地,在AC条件下,糖酵解途径(EMP)和三羧酸(TCA)循环的大多数分解代谢基因的转录水平高于AN条件,这表明米曲霉在AC条件下使用EMP和TCA进行葡萄糖代谢。我们通过使用包括麦麸在内的三种工业固相生物质介质,进一步研究了编码水解酶和参与能量分解代谢的酶的基因的表达。在三种测试培养基中,小麦麸皮培养物提供了最丰富的水解酶基因表达谱和最低的分解代谢基因(EMP,TCA)表达水平。麦麸培养物中分解代谢基因的低表达水平可能释放分解代谢物阻遏,因此导致水解酶的丰富表达谱。

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  • 来源
    《酒類総合研究所報告》 |2005年第177期|p.169-178|共10页
  • 作者单位

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan,The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan,Tohoku Technoarch Co. Ltd, Sendai, 981-0845, Japan;

    Research Center for Glycoscience, National Institute of Advanced Industrial Science and Technology, Tsukuba, 305-8566, Japan;

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan,The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan;

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan;

    National Research Institute of Brewing, Higashi-Hiroshima, 739-0046, Japan;

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan;

    Industrial Technology Institute, Miyagi Prefectural Government, Sendai, 981-3206, Japan;

    Industrial Technology Institute, Miyagi Prefectural Government, Sendai, 981-3206, Japan;

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan,The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan;

    Research Center for Glycoscience, National Institute of Advanced Industrial Science and Technology, Tsukuba, 305-8566, Japan;

    National Research Institute of Brewing, Higashi-Hiroshima, 739-0046, Japan;

    The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan;

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan;

    The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan;

    Department of Molecular and Cell Biology, Graduate School of Agricultural Science, Tohoku University, 1-1 Amamiya, Tsutsumi-dori, Sendai, 981-8555, Japan,The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan;

    The New Industry Creation Hatchery Center, Tohoku University, Sendai, 980-8579, Japan;

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