湖北假酵母菌BOT-O的功能基因组注释和转录组分析。湖北假酵母菌BOT-O是一种利用葡萄糖和木糖的产油酵母

IF 2.4 3区 生物学 Q3 GENETICS & HEREDITY
Friederike Mierke , Daniel P. Brink , Joakim Norbeck , Verena Siewers , Thomas Andlid
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引用次数: 1

摘要

湖北假酵母菌(Pseudozyma hubeiensis)是一种担子菌酵母,具有木质纤维素增值的高度理想的特性,在利用葡萄糖和木糖方面同样有效,并且能够共同利用它们。该物种以前主要研究其以甘露糖赤藓糖醇脂质的形式分泌生物表面活性剂的能力,但它也是一种产油物种,能够在营养饥饿期间积累高水平的三酰甘油储存脂。在这项研究中,我们旨在通过评估以葡萄糖或木糖为碳源的储存脂质形成条件下湖北紫杉树的代谢和基因表达反应,进一步表征其产油特性。利用MinION长读测序技术对湖北猿猴BOT-O菌株基因组进行了测序,得到了迄今为止最接近的湖北猿猴基因组,全长18.95 Mb,共31个片段。利用转录组数据作为实验支持,我们建立了首个以mrna支持的湖北对虾基因组注释,并鉴定出6540个基因。80%的预测基因基于与其他酵母的蛋白质同源性被分配了功能注释。在此基础上,重构了BOT-O的关键代谢途径,包括储存脂质、甘露糖赤藓糖醇脂质和木糖同化途径。证实了BOT-O消耗葡萄糖和木糖的速率相同,但在葡萄糖-木糖混合培养过程中,葡萄糖被发现消耗得更快。差异表达分析表明,在木糖与葡萄糖培养、指数生长和氮饥饿培养过程中,只有122个基因在|log2倍变化|≥2的临界值下有显著差异表达。在这122个基因中,鉴定出在所有时间点差异表达的24个基因的核心集。氮饥饿导致了更大的转录效应,与葡萄糖或木糖的指数生长相比,共有1179个基因在指定的倍数变化截止点上发生了显著的表达变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional genome annotation and transcriptome analysis of Pseudozyma hubeiensis BOT-O, an oleaginous yeast that utilizes glucose and xylose at equal rates

Pseudozyma hubeiensis is a basidiomycete yeast that has the highly desirable traits for lignocellulose valorisation of being equally efficient at utilization of glucose and xylose, and capable of their co-utilization. The species has previously mainly been studied for its capacity to produce secreted biosurfactants in the form of mannosylerythritol lipids, but it is also an oleaginous species capable of accumulating high levels of triacylglycerol storage lipids during nutrient starvation. In this study, we aimed to further characterize the oleaginous nature of P. hubeiensis by evaluating metabolism and gene expression responses during storage lipid formation conditions with glucose or xylose as a carbon source.

The genome of the recently isolated P. hubeiensis BOT-O strain was sequenced using MinION long-read sequencing and resulted in the most contiguous P. hubeiensis assembly to date with 18.95 Mb in 31 contigs. Using transcriptome data as experimental support, we generated the first mRNA-supported P. hubeiensis genome annotation and identified 6540 genes. 80% of the predicted genes were assigned functional annotations based on protein homology to other yeasts. Based on the annotation, key metabolic pathways in BOT-O were reconstructed, including pathways for storage lipids, mannosylerythritol lipids and xylose assimilation. BOT-O was confirmed to consume glucose and xylose at equal rates, but during mixed glucose-xylose cultivation glucose was found to be taken up faster. Differential expression analysis revealed that only a total of 122 genes were significantly differentially expressed at a cut-off of |log2 fold change| ≥ 2 when comparing cultivation on xylose with glucose, during exponential growth and during nitrogen-starvation. Of these 122 genes, a core-set of 24 genes was identified that were differentially expressed at all time points. Nitrogen-starvation resulted in a larger transcriptional effect, with a total of 1179 genes with significant expression changes at the designated fold change cut-off compared with exponential growth on either glucose or xylose.

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来源期刊
Fungal Genetics and Biology
Fungal Genetics and Biology 生物-遗传学
CiteScore
6.20
自引率
3.30%
发文量
66
审稿时长
85 days
期刊介绍: Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny. Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists. Research Areas include: • Biochemistry • Cytology • Developmental biology • Evolutionary biology • Genetics • Molecular biology • Phylogeny • Physiology.
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