Miao Yuanyuan, Shen Yi, Xu Yong
Department of Bioengineering, College of Chemical Engineering, Nanjing Forestry UniversityNanjing, China.
Jiangsu Province Key Laboratory of Green Biomass-based Fuels and Chemicals, Nanjing Forestry UniversityNanjing, China.
Front Microbiol. 2017 Apr 25;8:716. doi: 10.3389/fmicb.2017.00716. eCollection 2017.
D-Xylonic acid belongs to the top 30 biomass-based platform chemicals and represents a promising application of xylose. Until today, NL71 is the most efficient microbe capable of fermenting xylose into xylonate. However, its growth is seriously inhibited when concentrated lignocellulosic hydrolysates are used as substrates due to the presence of various degraded compounds formed during biomass pretreatment. Three critical lignocellulosic inhibitors were thereby identified, i.e., formic acid, furfural, and 4-hydroxybenzaldehyde. As microbe fermentation is mostly regulated at the genome level, four groups of cell transcriptomes were obtained for a comparative investigation by RNA sequencing of a control sample with samples treated separately with the above-mentioned inhibitors. The digital gene expression profiles screened 572, 714 genes, and 408 DEGs was obtained by the comparisons among four transcriptomes. A number of genes related to the different functional groups showed characteristic expression patterns induced by three inhibitors, in which 19 genes were further tested and confirmed by qRT-PCR. We extrapolated many differentially expressed genes that could explain the cellular responses to the inhibitory effects. We provide results that enable the scientific community to better define the molecular processes involved in the microbes' responses to lignocellulosic inhibitors during the cellular biooxidation of xylose into xylonic acid.
D-木糖酸属于30种基于生物质的平台化学品之一,是木糖具有前景的应用产物。直至今日,NL71是最有效的能够将木糖发酵成木糖酸盐的微生物。然而,当使用浓缩木质纤维素水解产物作为底物时,由于生物质预处理过程中形成的各种降解化合物的存在,其生长受到严重抑制。由此确定了三种关键的木质纤维素抑制剂,即甲酸、糠醛和4-羟基苯甲醛。由于微生物发酵大多在基因组水平上受到调控,通过对对照样品与分别用上述抑制剂处理的样品进行RNA测序,获得了四组细胞转录组用于比较研究。数字基因表达谱筛选出572714个基因,通过四组转录组之间的比较获得了408个差异表达基因(DEGs)。许多与不同功能组相关的基因显示出由三种抑制剂诱导的特征性表达模式,其中19个基因通过qRT-PCR进一步测试和确认。我们推断出许多差异表达基因,这些基因可以解释细胞对抑制作用的反应。我们提供的结果使科学界能够更好地定义在木糖细胞生物氧化成木糖酸过程中微生物对木质纤维素抑制剂反应所涉及的分子过程。