太空生物再生。

L Wolf
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引用次数: 0

摘要

欧空局一直在研究一种小型生物再生系统,以支持航天器上的长期生物实验,包括氧气、水和食物。该系统的核心部件是一个特殊的光生物反应器,其中培养了一株产麦芽糖的绿藻小球藻。在最初的实验中,对这种生物反应器进行了测试,并对小球藻的生理进行了研究。确定了CO2到O2转化和麦芽糖生产的最佳条件,并确定了控制培养以满足消费者需求的可能性。一个微重力兼容的光生物反应器和一个麦芽糖分离器已经开发出来,并根据设计规范在地面上运行。未来还必须进行失重测试。这些组件将被整合到一个完整的生物再生生命支持系统中,然后将进行广泛的测试。EXEMSI项目提供了一个机会,研究小球藻培养物和真正的生物耗氧者,即隔离设施实验室模块中的四名机组人员之间的相互影响。小球藻241.80由机组人员在气升式生物反应器中分批培养25天,并从模块中吸入空气。机组人员测定了从培养液中提取的样品的pH值和细胞密度。显微镜观察显示培养物没有被其他生物污染的证据。生长速度比在实验室条件下观察到的要小。这是由于模块大气中的平均二氧化碳浓度相对较低:在实验室实验期间,空气供应中的二氧化碳浓度为0.1%,而不是0.5%。数据显示,在小球藻培养中没有微量污染物积累的证据。研究结果令人鼓舞,对系统的进一步模拟作战试验具有一定的参考价值。
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Bioregeneration in space.

ESA has been studying a small-scale bioregenerative system to support long-term biological experiments on-board spacecraft with oxygen, water, and food. Core component of this system is a special photo-bioreactor in which a maltose-producing strain of the green alga Chlorella is cultivated. In initial experiments this bioreactor has been tested, and the physiology of Chlorella has been studied. The optimal conditions for CO2 to O2 conversion and maltose production have been determined, and the possibility of controlling the culture so as to match the needs of the consumer has been established. A microgravity-compatible photo-bioreactor, and a maltose separator have been developed and are functioning on the ground according to the design specifications. Tests in weightlessness will have to be performed in the future. The components are to be integrated to a complete bioregenerative life support system, which will then be subjected to extensive testing. The EXEMSI project afforded an opportunity to study the mutual influence of a Chlorella culture and real biological oxygen consumers, the four crew members in the laboratory module of the isolation facility. Chlorella 241.80 was batch cultured in an airlift bioreactor by the crew for 25 days with air aspirated from the module. The crew members determined pH and cell density in samples withdrawn from the culture. Microscopic observations showed no evidence of contamination of the culture by other organisms. Growth rates were smaller than those observed in laboratory conditions. This is attributed to the relatively low average CO2 concentration in the module atmosphere: 0.1% against 0.5% in the air supply during the laboratory experiments. The data show no evidence of trace contaminant accumulation in the Chlorella culture. The results are encouraging and suggest the value of further simulated operational testing of the system.

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