Fang Ming, Sun Xu, Yao Fangjie, Lu Lixin, Ma Xiaoxu, Shao Kaisheng, Kaimoyo Evans
Lab of the Genetic Breeding of Edible Mushroom, College of Horticulture, Jilin Agricultural University, Changchun 130118, China.
Engineering Research Centre of Chinese Ministry of Education for Edible and Medicinal Fungi, Jilin Agricultural University, Changchun 130118, China.
J Fungi (Basel). 2024 Aug 3;10(8):545. doi: 10.3390/jof10080545.
The cultivation of , a species of edible mushroom, heavily relies on the availability of wood resources serving as substrate for the growth of the species. To ensure the sustainable development of the industry and optimize the utilization of corncob as a substrate, this study sought to investigate the potential use of corncob as a substrate for the cultivation of . The purpose of this study was to explore the utilization of corncob lignocellulose by at the mycelium, primordium, and fruiting stages, by specifically examining the expression profiles of both carbohydrate-active enzymes (CAZymes) and the transcriptome of differentially expressed genes (DEGs) relevant to corncob biomass degradation. The results revealed 10,979, 10,630, and 11,061 DEGs at the mycelium, primordium, and fruiting stages, respectively, while 639 DGEs were identified as carbohydrate-active enzymes. Of particular interest were 46 differentially expressed CAZymes genes that were associated directly with lignocellulose degradation. Furthermore, the study found that A. heimuer exhibited adaptive changes that enabled it to effectively utilize the cellulose present in the corncob. These changes were observed primarily at the primordium and fruiting stages. Key genes involved in lignocellulose degradation were also identified, including , , , and at the mycelium stage, , , , and at the primordium stage, and , , , , and at the fruiting stage. This study found that lytic polysaccharide monooxygenase (LPMO) played a crucial role in the degradation of corncob cellulose, further highlighting the complexity of the molecular mechanisms involved in the degradation of lignocellulose biomass by . The study sheds light on the molecular mechanisms underlying the ability of to degrade corncob biomass, with implications for the efficient utilization of lignocellulose resources. The findings from this study may facilitate the development of innovative biotechnologies for the transformation of corncob biomass into useful products.
黑木耳是一种食用菌,其栽培严重依赖作为该物种生长基质的木材资源。为确保黑木耳产业的可持续发展并优化玉米芯作为基质的利用,本研究旨在探究玉米芯作为黑木耳栽培基质的潜在用途。本研究的目的是通过具体检测与玉米芯生物质降解相关的碳水化合物活性酶(CAZymes)的表达谱和差异表达基因(DEGs)的转录组,来探索黑木耳在菌丝体、原基和子实体阶段对玉米芯木质纤维素的利用情况。结果显示,在菌丝体、原基和子实体阶段分别有10,979、10,630和11,061个差异表达基因,同时有639个差异表达基因被鉴定为碳水化合物活性酶。特别值得关注的是46个与木质纤维素降解直接相关的差异表达CAZymes基因。此外,该研究发现黑木耳表现出适应性变化,使其能够有效利用玉米芯中存在的纤维素。这些变化主要在原基和子实体阶段观察到。还鉴定了参与木质纤维素降解的关键基因,包括菌丝体阶段的[具体基因1]、[具体基因2]、[具体基因3]和[具体基因4],原基阶段的[具体基因5]、[具体基因6]、[具体基因7]和[具体基因8],以及子实体阶段的[具体基因9]、[具体基因10]、[具体基因11]、[具体基因12]和[具体基因13]。本研究发现裂解多糖单加氧酶(LPMO)在玉米芯纤维素降解中起关键作用,进一步凸显了黑木耳降解木质纤维素生物质所涉及分子机制的复杂性。该研究揭示了黑木耳降解玉米芯生物质能力背后的分子机制,对木质纤维素资源的高效利用具有启示意义。本研究的结果可能有助于开发将玉米芯生物质转化为有用产品的创新生物技术。