{"title":"低温等离子体诱导酿酒酵母在常压下提高乙醇产量的研究","authors":"X. Dong","doi":"10.5772/INTECHOPEN.78019","DOIUrl":null,"url":null,"abstract":"In this study, cold plasma at atmospheric pressure, as a novel approach of bioprocess intensification, was used to induce yeast for the improvement of ethanol production. Response surface methodology (RSM) was used to optimize the discharge-associated parameters of cold plasma for the purpose of maximizing the ethanol yield achieved by cold plasma-treated S. cerevisiae. The resulting yield of ethanol reached to 0.48 g g−1 under optimized parameters of plasma exposure time of 1 min, power voltage of 26 V, and an exposed sample volume of 9 mL, which represented an increase of 33% over control. Compared with non-exposed cells, cells exposed with plasma for 1 min presented a notable increment in cytoplasmic free Ca2+, when these exposed cells showed the significant increase in membrane potential. At the same time, ATP level decreased by about 40%, resulting in about 60% reduction in NADH. Taken together, these data suggested that the mechanism that air cold plasma raised plasma membrane potential, which led to increases in cytosolic Ca2+ concentration. Furthermore, the cofactor metabolism, such as ATP and NADH, was subjected to regulation that was mediated by Ca2+, ultimately improving yeast productivity. This may have a underlying and broad utilization in enhancing bioconversion capability of microbe in the next few years.","PeriodicalId":12484,"journal":{"name":"Fuel Ethanol Production from Sugarcane","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Enhanced Ethanol Production of Saccharomyces cerevisiae Induced by Cold Plasma at Atmospheric Air Pressure\",\"authors\":\"X. Dong\",\"doi\":\"10.5772/INTECHOPEN.78019\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, cold plasma at atmospheric pressure, as a novel approach of bioprocess intensification, was used to induce yeast for the improvement of ethanol production. Response surface methodology (RSM) was used to optimize the discharge-associated parameters of cold plasma for the purpose of maximizing the ethanol yield achieved by cold plasma-treated S. cerevisiae. The resulting yield of ethanol reached to 0.48 g g−1 under optimized parameters of plasma exposure time of 1 min, power voltage of 26 V, and an exposed sample volume of 9 mL, which represented an increase of 33% over control. Compared with non-exposed cells, cells exposed with plasma for 1 min presented a notable increment in cytoplasmic free Ca2+, when these exposed cells showed the significant increase in membrane potential. At the same time, ATP level decreased by about 40%, resulting in about 60% reduction in NADH. Taken together, these data suggested that the mechanism that air cold plasma raised plasma membrane potential, which led to increases in cytosolic Ca2+ concentration. Furthermore, the cofactor metabolism, such as ATP and NADH, was subjected to regulation that was mediated by Ca2+, ultimately improving yeast productivity. This may have a underlying and broad utilization in enhancing bioconversion capability of microbe in the next few years.\",\"PeriodicalId\":12484,\"journal\":{\"name\":\"Fuel Ethanol Production from Sugarcane\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fuel Ethanol Production from Sugarcane\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5772/INTECHOPEN.78019\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Ethanol Production from Sugarcane","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5772/INTECHOPEN.78019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
摘要
在本研究中,低温等离子体作为一种新的生物过程强化方法,用于诱导酵母提高乙醇产量。采用响应面法(RSM)对冷等离子体放电相关参数进行优化,以使冷等离子体处理酿酒酵母的乙醇产量最大化。在等离子体暴露时间为1 min、电源电压为26 V、暴露样品量为9 mL的优化条件下,乙醇得率达到0.48 g g−1,比对照提高了33%。与未暴露的细胞相比,暴露于血浆1min的细胞胞质游离Ca2+显著增加,膜电位显著升高。同时,ATP水平下降约40%,导致NADH降低约60%。综上所述,这些数据表明,空气冷等离子体提高质膜电位的机制,导致细胞质Ca2+浓度增加。此外,辅助因子代谢,如ATP和NADH,受到Ca2+介导的调节,最终提高酵母产量。这在提高微生物的生物转化能力方面具有潜在和广泛的应用前景。
Enhanced Ethanol Production of Saccharomyces cerevisiae Induced by Cold Plasma at Atmospheric Air Pressure
In this study, cold plasma at atmospheric pressure, as a novel approach of bioprocess intensification, was used to induce yeast for the improvement of ethanol production. Response surface methodology (RSM) was used to optimize the discharge-associated parameters of cold plasma for the purpose of maximizing the ethanol yield achieved by cold plasma-treated S. cerevisiae. The resulting yield of ethanol reached to 0.48 g g−1 under optimized parameters of plasma exposure time of 1 min, power voltage of 26 V, and an exposed sample volume of 9 mL, which represented an increase of 33% over control. Compared with non-exposed cells, cells exposed with plasma for 1 min presented a notable increment in cytoplasmic free Ca2+, when these exposed cells showed the significant increase in membrane potential. At the same time, ATP level decreased by about 40%, resulting in about 60% reduction in NADH. Taken together, these data suggested that the mechanism that air cold plasma raised plasma membrane potential, which led to increases in cytosolic Ca2+ concentration. Furthermore, the cofactor metabolism, such as ATP and NADH, was subjected to regulation that was mediated by Ca2+, ultimately improving yeast productivity. This may have a underlying and broad utilization in enhancing bioconversion capability of microbe in the next few years.