He-Ne激光与脉冲光突变菌丝体菌丝生长相关候选基因的转录组对比分析

Yating Dong, Haile Ma, ling Sun, ronghai He, xiaofei Ye, bingcheng Gan
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引用次数: 0

摘要

利用氦氖激光脉冲光照射技术筛选到一株菌丝产量较高的突变体Phellinus igniarius JQ9,但其产生菌丝的机制尚不清楚。本研究旨在获得Ph. igniarius液体发酵过程中完整的转录组组合,并表征Ph. igniarius JQ9菌丝生长和代谢相关的关键基因。我们使用Illumina平台比较转录组测序技术获得了Ph. iniarius JQ9和野生菌株的转录组数据。结果表明,在346个差异表达基因(deg)中,245个表达上调,101个表达下调。候选基因编码内切葡聚糖酶、β -葡萄糖苷酶、纤维素1,4- β -纤维素生物苷酶、糖苷水解酶家族61蛋白,参与了Ph. igniarius JQ9从KEGG富集淀粉和蔗糖代谢途径的碳水化合物利用。此外,3个编码漆酶的候选基因和另外2个与细胞生长相关的候选基因在Ph. igniarius JQ9中的表达量高于野生型菌株(CK)。这些数据的分析表明,增加这些相关的碳水化合物代谢候选基因的一个关键途径可能导致更高的菌丝产量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Transcriptome Analysis of Candidate Genes Associated with Mycelia Growth from a He-Ne Laser with Pulsed Light Mutant of Phellinus igniarius (Agaricomycetes)
A mutant Phellinus igniarius JQ9 with higher mycelial production was screened out by He-Ne laser with pulsed light irradiation, the mechanism underlying the higher mycelial production is still unknow. This study aims to obtain a comprehensive transcriptome assembly during the Ph. igniarius liquid fermentation and characterize the key genes associated with the mycelial growth and metabolism in Ph. igniarius JQ9. Our transcriptome data of Ph. iniarius JQ9 and the wild strain were obtained with the Illumina platform comparative transcriptome sequencing technology. The results showed that among all the 346 differentially expressed genes (DEGs), 245 were up-regulated and 101 were down-regulated. Candidate genes encoding endoglucanase, beta-glucosidase, cellulose 1,4-beta-cellobiosidase, glycoside hydrolase family 61 protein, were proposed to participate in the carbohydrate utilization from KEGG enrichment of the starch and sucrose metabolism pathways were up-regulated in Ph. igniarius JQ9. In addition, three candidate genes encoding the laccase and another two candidate genes related with the cell growth were higher expressed in Ph. igniarius JQ9 than in the wild type of strain (CK). Analysis of these data revealed that increased these related carbohydrate metabolism candidate genes underlying one crucial way may cause the higher mycelia production.
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