Yang Jian, Tang Qilong, Xu Lei, Li Zhijiang, Ma Yongqiang, Yao Di
Department of Food and Engineering College of Food Engineering Harbin University of Commerce Harbin China.
Department of Food and Engineering College of Food Heilongjiang Bayi Agricultural University Daqing China.
Food Sci Nutr. 2019 Sep 30;7(11):3480-3493. doi: 10.1002/fsn3.1194. eCollection 2019 Nov.
A combination of transcriptome and metabolome analyses was applied to understand the utilization and metabolism of Xylo-oligosaccharide (XOS) in 15703 as well as identifying the key regulatory-related genes and metabolites. Samples of cultures grown on either XOS or xylose were collected. The transcript and metabolite profiles were obtained from high-throughput RNA-sequencing data analysis and UHPLC system. Compared with xylose, XOS highly promoted the growth of 15703 and resulted in a growth yield about 1.5-fold greater than xylose. The transcriptome analysis showed that XOS could enhance genes, including ABC transporters, galactosidase, xylosidase, glucosidase, and amylase, which were involved in transport and metabolism of carbohydrate compared with xylose. Furthermore, the expression profile of 16 candidate genes using qRT-PCR has validated the accuracy of the RNA-seq data. Also, the metabolomic analyses, particularly those related to metabolic biomarkers of fatty acids, amino acids, and sugars showed a similar trend of result and approved the advantages of XOS as growth medium for 15703 compared with xylose. The expression and abundance of specific genes and metabolites highlighted the complex regulatory mechanisms involved in utilization of XOS by 15703. These results are useful in the understanding of the metabolic pathway of XOS in 15703 and contribute to the optimization of XOS probiotic effects as a food additive.
采用转录组和代谢组分析相结合的方法,以了解15703中低聚木糖(XOS)的利用和代谢情况,并鉴定关键调控相关基因和代谢物。收集在XOS或木糖上生长的培养物样本。通过高通量RNA测序数据分析和超高效液相色谱系统获得转录本和代谢物谱。与木糖相比,XOS显著促进了15703的生长,生长产量比木糖高出约1.5倍。转录组分析表明,与木糖相比,XOS可以增强包括ABC转运蛋白、半乳糖苷酶、木糖苷酶、葡萄糖苷酶和淀粉酶在内的基因表达,这些基因参与碳水化合物的运输和代谢。此外,使用qRT-PCR对16个候选基因的表达谱分析验证了RNA-seq数据的准确性。代谢组学分析,特别是与脂肪酸、氨基酸和糖类代谢生物标志物相关的分析,也显示出类似的结果趋势,并证实了与木糖相比,XOS作为15703生长培养基的优势。特定基因和代谢物的表达及丰度突出了15703利用XOS所涉及的复杂调控机制。这些结果有助于了解15703中XOS的代谢途径,并有助于优化XOS作为食品添加剂的益生菌效果。