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Cost-effective production of C-13, N-15 stable isotope-labelled biomass from phototrophic microalgae for various biotechnological applications

机译:从光养性微藻中经济高效地生产C-13,N-15稳定同位素标记的生物质,用于各种生物技术应用

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The present study outlines a process for the cost-effective production of C-13/N-15-labelled biomass of microalgae on a commercial scale. The core of the process is a bubble column photobioreactor with exhaust gas recirculation by means of a low-pressure compressor. To avoid accumulation of dissolved oxygen in the culture, the exhaust gas is bubbled through a sodium sulphite solution prior to its return to the reactor. The engineered system can be used for the production of C-13, N-15, and C-13-N-15 stable isotope-labelled biomass as required. To produce C-13-labelled biomass, (CO2)-C-13 is injected on demand for pH control and carbon supply, whereas for N-15-labelled biomass (NaNO3)-N-15 is supplied as nitrogen source at the stochiometric concentration. The reactor is operated in semicontinuous mode at different biomass concentrations, yielding a maximum mean biomass productivity of 0.3 g L-1 day(-1). In order to maximize the uptake efficiency of the labelled substrates, the inorganic carbon is recovered from the supernatant by acidification/desorption processes, while the nitrate is delivered at stochiometric concentration and the harvesting of biomass is performed when the (NO3-)-N-15 is depleted. In these conditions, elemental analysis of both biomass and supernatant shows that 89.2% of the injected carbon is assimilated into the biomass and 6.9% remains in the supernatant. Based on elemental analysis, 97.8% of the supplied nitrogen is assimilated into the biomass and 1.3% remains in the supernatant. Stable isotope-labelling enrichment has been analysed by GC-MS results showing that the biomass is highly labelled. All the fatty acids are labelled; more than 96% of the carbon present in these fatty acids is C-13. The engineered system was stably operated for 3 months, producing over 160 g of C-13 and/or N-15-labelled biomass. The engineered bioreactor can be applied for the labelling of various microalgae. (C) 2005 Elsevier B.V. All rights reserved.
机译:本研究概述了以商业规模经济有效地生产C-13 / N-15标记微藻生物质的方法。该方法的核心是气泡塔光生物反应器,该气体生物反应器通过低压压缩机进行废气再循环。为了避免培养物中溶解氧的积累,在将废气返回到反应器之前,将其鼓泡通过亚硫酸钠溶液。根据需要,该工程系统可用于生产C-13,N-15和C-13-N-15稳定的同位素标记生物质。为了生产C-13标记的生物质,可根据需要注入(CO2)-C-13以控制pH和供应碳,而对于N-15标记的生物质(NaNO3)-N-15作为氮源以化学计量方式提供浓度。该反应器在不同的生物质浓度下以半连续模式运行,产生的最大平均生物质生产率为0.3 g L-1天(-1)。为了最大化标记底物的吸收效率,无机酸通过酸化/解吸过程从上清液中回收,而硝酸盐以化学计量浓度输送,当(NO3-)-N- 15已耗尽。在这些条件下,对生物质和上清液的元素分析表明,注入的碳中有89.2%被吸收到生物质中,而6.9%保留在上清液中。根据元素分析,所提供的氮的97.8%被吸收到生物质中,而1.3%保留在上清液中。通过GC-MS分析了稳定的同位素标记富集,结果表明生物质被高度标记。所有的脂肪酸都有标签;这些脂肪酸中超过96%的碳是C-13。该工程系统稳定运行了3个月,产生了160克C-13和/或N-15标记的生物质。工程生物反应器可用于各种微藻的标记。 (C)2005 Elsevier B.V.保留所有权利。

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