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首页> 外文期刊>Biotechnology Progress >CO2 from Alcoholic Fermentation for Continuous Cultivation of Arthrospira (Spirulina) platensis in Tubular Photobioreactor Using Urea as Nitrogen Source
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CO2 from Alcoholic Fermentation for Continuous Cultivation of Arthrospira (Spirulina) platensis in Tubular Photobioreactor Using Urea as Nitrogen Source

机译:尿素为氮源的酒精发酵二氧化碳在管状光生物反应器中连续培养节杆菌(Spirulina)

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Carbon dioxide released from alcoholic fermentation accounts for 33% of the whole CO2 involved in the use of ethanol as fuel derived from glucose. As Arthrospira platensis can uptake this greenhouse gas, this study evaluates the use of the CO2 released from alcoholic fermentation for the production of Arthrospira platensis. For this purpose, this cyanobacte-rium was cultivated in continuous process using urea as nitrogen source, either using CO2 from alcoholic fermentation, without any treatment, or using pure CO2 from cylinder. The experiments were carried out at 120 μmol photons m~~(-2) s~(-1) in tubular photobioreactor at different dilution rates (0.2 ≤ D ≤ 0.8 d~(-1) ). Using CO2 from alcoholic fermentation, maximum steady-state cell concentration (2661 ± 71 mg L~(-1)) was achieved at D = 0.2 d~(-1), whereas higher dilution rate (0.6 d~(-1)) was needed to maximize cell productivity (839 mg L~(-1) d~(-1)). This value was 10% lower than the one obtained with pure CO2, and there was no significant difference in the biomass protein content. With D = 0.8 d~(-1), it was possible to obtain 56% ± 1.5% and 50% ± 1.2% of protein in the dry biomass, using pure CO2 and CO2 from alcoholic fermentation, respectively. These results demonstrate that the use of such cost free CO2 from alcoholic fermentation as carbon source, associated with low cost nitrogen source, may be a promising way to reduce costs of continuous cultivation of photo-synthetic microorganisms, contributing at the same time to mitigate the greenhouse effect.
机译:酒精发酵释放的二氧化碳占使用乙醇作为葡萄糖燃料的二氧化碳总量的33%。由于Arthrospira platensis可以吸收这种温室气体,因此本研究评估了酒精发酵释放的CO2在生产Arthrospira platensis中的用途。为此目的,使用尿素作为氮源,使用酒精发酵产生的二氧化碳,不经任何处理,或使用钢瓶中的纯二氧化碳,以连续过程培养该氰化细菌-。实验是在管状光生物反应器中以120μmol光子m ~~(-2)s〜(-1)在不同稀释率(0.2≤D≤0.8 d〜(-1))下进行的。使用酒精发酵产生的二氧化碳,当D = 0.2 d〜(-1)时,达到最大稳态细胞浓度(2661±71 mg L〜(-1)),而更高的稀释率(0.6 d〜(-1))。需要最大限度地提高细胞生产率(839 mg L〜(-1)d〜(-1))。该值比用纯CO2获得的值低10%,并且生物量蛋白质含量没有显着差异。当D = 0.8 d〜(-1)时,分别使用酒精发酵产生的纯CO2和CO2,可以在干燥生物质中获得56%±1.5%和50%±1.2%的蛋白质。这些结果表明,使用这种来自酒精发酵的无成本的二氧化碳作为碳源,再加上低成本的氮源,可能是降低光合微生物连续培养成本的有前途的方法,同时有助于减轻温室效应。

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