Li Chunsheng, Liu Qiuying, Wang Yueqi, Yang Xianqing, Chen Shengjun, Zhao Yongqiang, Wu Yanyan, Li Laihao
Key Laboratory of Aquatic Product Processing, Ministry of Agriculture and Rural Affairs, National R&D Center for Aquatic Product Processing, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou, 510300, China.
Co-Innovation Center of Jiangsu Marine Bio-Industry Technology, Jiangsu Ocean University, Lianyungang, 222005, China.
Biotechnol Biofuels. 2021 Nov 25;14(1):222. doi: 10.1186/s13068-021-02071-0.
High-temperature bioethanol production benefits from yeast thermotolerance. Salt stress could induce obvious cross-protection against heat stress of Pichia kudriavzevii, contributing to the improvement of its thermotolerance and bioethanol fermentation. However, the underlying mechanisms of the cross-protection remain poorly understood.
Salt stress showed obvious cross-protection for thermotolerance and high-temperature ethanol production of P. kudriavzevii observed by biomass, cell morphology and bioethanol production capacity. The biomass and ethanol production of P. kudriavzevii at 45 °C were, respectively, improved by 2.6 and 3.9 times by 300 mmol/L NaCl. Metabolic network map showed that salt stress obviously improved the key enzymes and intermediates in carbohydrate metabolism, contributing to the synthesis of bioethanol, ATP, amino acids, nucleotides, and unsaturated fatty acids, as well as subsequent intracellular metabolisms. The increasing trehalose, glycerol, HSPs, and ergosterol helped maintain the normal function of cell components. Heat stress induced serious oxidative stress that the ROS-positive cell rate and dead cell rate, respectively, rose from 0.5% and 2.4% to 28.2% and 69.2%, with the incubation temperature increasing from 30 to 45 °C. The heat-induced ROS outburst, oxidative damage, and cell death were obviously inhibited by salt stress, especially the dead cell rate which fell to only 20.3% at 300 mmol/L NaCl. The inhibiting oxidative damage mainly resulted from the abundant synthesis of GSH and GST, which, respectively, increased by 4.8 and 76.1 times after addition of 300 mmol/L NaCl. The improved bioethanol production was not only due to the improved thermotolerance, but resulted from the up-regulated alcohol dehydrogenases and down-regulated aldehyde dehydrogenases by salt stress.
The results provide a first insight into the mechanisms of the improved thermotolerance and high-temperature bioethanol production of P. kudriavzevii by salt stress, and provide important information to construct genetic engineering yeasts for high-temperature bioethanol production.
高温生物乙醇生产受益于酵母的耐热性。盐胁迫可诱导库德里阿兹威毕赤酵母对热胁迫产生明显的交叉保护作用,有助于提高其耐热性和生物乙醇发酵能力。然而,交叉保护的潜在机制仍知之甚少。
通过生物量、细胞形态和生物乙醇生产能力观察发现,盐胁迫对库德里阿兹威毕赤酵母的耐热性和高温乙醇生产表现出明显的交叉保护作用。300 mmol/L NaCl使库德里阿兹威毕赤酵母在45℃时的生物量和乙醇产量分别提高了2.6倍和3.9倍。代谢网络图显示,盐胁迫明显改善了碳水化合物代谢中的关键酶和中间产物,有助于生物乙醇、ATP、氨基酸、核苷酸和不饱和脂肪酸的合成以及随后的细胞内代谢。海藻糖、甘油、热休克蛋白和麦角固醇的增加有助于维持细胞成分的正常功能。热胁迫诱导严重的氧化应激,随着培养温度从30℃升高到45℃,活性氧阳性细胞率和死细胞率分别从0.5%和2.4%升至28.2%和69.2%。盐胁迫明显抑制了热诱导的活性氧爆发、氧化损伤和细胞死亡,尤其是在300 mmol/L NaCl时死细胞率降至仅20.3%。抑制氧化损伤主要源于谷胱甘肽和谷胱甘肽-S-转移酶的大量合成,添加300 mmol/L NaCl后分别增加了4.8倍和76.1倍。生物乙醇产量的提高不仅归因于耐热性的提高,还源于盐胁迫使乙醇脱氢酶上调和醛脱氢酶下调。
该结果首次深入了解了盐胁迫提高库德里阿兹威毕赤酵母耐热性和高温生物乙醇生产的机制,并为构建用于高温生物乙醇生产的基因工程酵母提供了重要信息。