食品科学 ›› 2018, Vol. 39 ›› Issue (12): 167-173.doi: 10.7506/spkx1002-6630-201812026

• 生物工程 • 上一篇    下一篇

糖胁迫下鲁氏接合酵母的代谢指纹分析

韩晓江,徐志娇,岳田利,牛晨,魏建平,蔡瑞*,袁亚宏*   

  1. (西北农林科技大学食品科学与工程学院,陕西?杨凌 712100)
  • 出版日期:2018-06-25 发布日期:2018-06-15
  • 基金资助:
    国家科技部-港澳台科技合作项目(2015DFT30130);陕西省科技攻关项目(2016KTCQ03-12)

Metabolic Fingerprinting Analysis of Zygosaccharomyces rouxii under Sugar Stress

HAN Xiaojiang, XU Zhijiao, YUE Tianli, NIU Chen, WEI Jianping, CAI Rui*, YUAN Yahong*   

  1. (College of Food Science and Engineering, Northwest A&F University, Yangling 712100, China)
  • Online:2018-06-25 Published:2018-06-15

摘要: 以高糖渗透压培养基(高渗培养条件,糖质量分数80%)和基本培养基分别培养鲁氏接合酵母,采用紫外-可见分光光度计测定其生长OD值的变化,采用硅烷化衍生-气相色谱-质谱联用技术检测酵母胞内物质成分,采用顶空固相微萃取和气相色谱-质谱联用技术检测胞外物质成分,并用主成分分析(principal components analysis,PCA)、正交偏最小二乘方判别分析(partial least squares discriminant analysis,PLS-DA)模型对其分析。结果表明,高渗培养条件下鲁氏接合酵母呈对数生长,在对数期取样,测得胞外物质共36?种;基本培养条件下的鲁氏接合酵母测得胞外物质共47?种;基本培养条件下的酿酒酵母测得胞外物质共45?种。在高渗环境下,鲁氏接合酵母以醇类、酯类居多,没有产生酮类化合物。PCA模型可以完全把3?个样本分开,说明差异性显著。PLS-DA模型的R2、Q2都接近1,说明可信度较高,并通过VIP(variable importance in the projection)值挑选出高渗培养条件下鲁氏接合酵母的特征性物质7-辛烯酸乙酯、3-(甲硫基)丙基乙酸酯、2-十三烷醇、十五烷酸-3-甲基丁酯、9-癸烯酸乙酯、3-(甲硫基)-1-丙醇、2-癸醇。鲁氏接合酵母胞内物质共检测出83?种,高渗培养条件和基本培养条件下鲁氏接合酵母相同物质有23?种,高渗培养条件下鲁氏接合酵母差异性物质有27?种,差异性物质说明鲁氏接合酵母能够耐高渗透压,会产生一些糖类、醇类、酸类等物质来保护细胞使其能够在高渗培养条件下生长,这些物质涉及糖代谢、能量代谢等。研究结果为今后研究鲁氏接合酵母耐高糖渗透压方面提供理论依据。

关键词: 鲁氏接合酵母, 高糖渗透压, 硅烷化衍生, 顶空固相微萃取法, 气相色谱-质谱法

Abstract: In this study, Zygosaccharomyces rouxii was cultured in hypertonic medium (80% sugar content) and basic medium, respectively. Optical density was monitored by a UV-Vis spectrophotometer for examining the growth of Z. rouxii. The intracellular materials were identified by silylation derivatization-gas chromatography-mass spectrometry (GC-MS). The extracellular substances were identified by head-space solid phase micro-extraction (HS-SPME) coupled to GC-MS. The data were analyzed by principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA). The results showed that the OD value of Z. rouxii increased logarithmically with culture time in high glucose medium. Thirty-six and 47 extracellular substances were identified from Z. rouxii at the logarithmic phase in high glucose medium and basic medium, respectively, and 45 extracellular substances were produced by Saccharomyces cerevisiae at the logarithmic phase in basic medium. Under hyperosmotic conditions, Z. rouxii mainly produced alcohols and esters, but did not produce ketones. The three samples were clearly discriminated by PCA, indicating significant differences among them. Both the R2 and Q2 of the PLS-DA model were close to 1, indicating high reliability. The characteristic substances of Z. rouxii under hypertonic condition including 7-octenoic acid ethyl ester, 3-(methylthio) propyl acetate, 2-tridecanol, pentadecanoic acid 3-methylbutyl ester, 9-decenoate, 3-(methylthio)-1-propanol, 2-decanol were selected based on variable importance in the projection (VIP) value. 83 intracellular components were identified, and 23 of these compounds were detected to present in both cultures. A total of 27 intracellular substances were found to exhibit significant differences between these two cultures, suggesting that Z. rouxii is able to withstand high osmotic pressure by producing some sugars, alcohols, acids and other substances involved in sugar metabolism and energy metabolism. The results of this study can provide a theoretical basis for further insights into the resistance of Z. rouxii to osmotic pressure.

Key words: Zygosaccharomyces rouxii, high sugar osmotic pressure, silylation derivatization, head-space solid phase micro-extraction (HS-SPME), gas chromatography-mass spectrometry (GC-MS)

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