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迈向无水生物库:在空气中干燥的昆虫细胞中,对脱水敏感的酶荧光素在室温下进行无水分的长期干燥保存。

Towards water-free biobanks: long-term dry-preservation at room temperature of desiccation-sensitive enzyme luciferase in air-dried insect cells.

机构信息

Graduate School of Bio-Applications and Systems Engineering, Tokyo University of Agriculture and Technology, Koganei, Tokyo, 184-8588, Japan.

Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa, 230-0045, Japan.

出版信息

Sci Rep. 2017 Jul 26;7(1):6540. doi: 10.1038/s41598-017-06945-y.

Abstract

Desiccation-tolerant cultured cells Pv11 derived from the anhydrobiotic midge embryo endure complete desiccation in an ametabolic state and resume their metabolism after rehydration. These features led us to develop a novel dry preservation technology for enzymes as it was still unclear whether Pv11 cells could preserve an exogenous enzyme in the dry state. This study shows that Pv11 cells protect an exogenous desiccation-sensitive enzyme, luciferase (Luc), preserving the enzymatic activity even after dry storage for 372 days at room temperature. A process including preincubation with trehalose, dehydration, storage, and rehydration allowed Pv11 (Pv11-Luc) cells stably expressing luciferase to survive desiccation and still emit luminescence caused by luciferase after rehydration. Luminescence produced by luciferase in Pv11-Luc cells after rehydration did not significantly decrease in presence of a translation inhibitor, showing that the activity did not derive from de novo enzyme synthesis following the resumption of cell metabolism. These findings indicate that the surviving Pv11 cells almost completely protect luciferase during desiccation. Lacking of the preincubation step resulted in the loss of luciferase activity after rehydration. We showed that preincubation with trehalose associated to induction of desiccation tolerance-related genes in Pv11 cells allowed effective in vivo preservation of enzymes in the dry state.

摘要

耐旱培养细胞 Pv11 源自休眠状态的摇蚊胚胎,可在无代谢状态下耐受完全干燥,并在再水合后恢复其代谢。这些特性使我们开发了一种新型的酶干燥保存技术,因为仍不清楚 Pv11 细胞是否可以在干燥状态下保存外源酶。本研究表明,Pv11 细胞可保护外源干燥敏感酶——荧光素酶(Luc),即使在室温下干燥储存 372 天后,仍能保持酶活性。包括用海藻糖预孵育、脱水、储存和再水合在内的过程使稳定表达荧光素酶的 Pv11(Pv11-Luc)细胞能够在干燥条件下存活,并在再水合后仍能发出由荧光素酶引起的荧光。在再水合后,Pv11-Luc 细胞中的荧光素酶产生的发光在存在翻译抑制剂的情况下没有显著降低,这表明该活性不是细胞代谢恢复后从头合成酶的结果。这些发现表明,在干燥过程中,存活的 Pv11 细胞几乎完全保护了荧光素酶。缺少预孵育步骤会导致再水合后荧光素酶活性丧失。我们表明,在 Pv11 细胞中用海藻糖预孵育并诱导与干燥耐受性相关的基因表达,可允许在干燥状态下有效地在体内保存酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/663a/5529557/8ef8315fbd5b/41598_2017_6945_Fig1_HTML.jpg

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