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Preservation of H2 production activity in nanoporous latex coatings of Rhodopseudomonas palustris CGA009 during dry storage at ambient temperatures

机译:在室温干燥贮藏期间保存沼泽红假单胞菌CGa009纳米多孔乳胶涂层中H2产生活性

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摘要

To assess the applicability of latex cell coatings as an u27off-the-shelfu27 biocatalyst, the effect of osmoprotectants, temperature, humidity and O(2) on preservation of H(2) production in Rhodopseudomonas palustris coatings was evaluated. Immediately following latex coating coalescence (24 h) and for up to 2 weeks of dry storage, rehydrated coatings containing different osmoprotectants displayed similar rates of H(2) production. Beyond 2 weeks of storage, sorbitol-treated coatings lost all H(2) production activity, whereas considerable H(2) production was still detected in sucrose- and trehalose-stabilized coatings. The relative humidity level at which the coatings were stored had a significant impact on the recovery and subsequent rates of H(2) production. After 4 weeks storage under air at 60% humidity, coatings produced only trace amounts of H(2) (0-0.1% headspace accumulation), whereas those stored at u3c 5% humidity retained 27-53% of their H(2) production activity after 8 weeks of storage. When stored in argon at u3c 5% humidity and room temperature, R. palustris coatings retained full H(2) production activity for 3 months, implicating oxidative damage as a key factor limiting coating storage. Overall, the results demonstrate that biocatalytic latex coatings are an attractive cell immobilization platform for preservation of bioactivity in the dry state.
机译:为了评估乳胶细胞涂层作为现成的生物催化剂的适用性,评估了渗透保护剂,温度,湿度和O(2)对红假单胞菌涂层中H(2)生产的保存的影响。乳胶涂料合并后立即固化(24小时),并在长达2周的干燥存储中,包含不同渗透防护剂的复水涂料显示出相似的H(2)生成速率。超过2周的存储,山梨糖醇处理过的涂料丧失了所有H(2)的生产活性,而在蔗糖和海藻糖稳定的涂料中仍检测到相当多的H(2)产生。储存涂料的相对湿度水平对H(2)的回收率和后续速率产生了重大影响。在空气中以60%的湿度存储4周后,涂层仅产生痕量的H(2)(0-0.1%的顶空积累),而在 u3c 5%湿度下存储的涂层保留其H(2)的27-53%储存8周后的生产活动。当在5%的湿度和室温下于氩气中存储时,R。ustustris涂料保留了完整的H(2)生产活性达3个月,这暗示氧化损伤是限制涂料存储的关键因素。总体而言,结果表明生物催化胶乳涂料是一种在干燥状态下保持生物活性的有吸引力的细胞固定平台。

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