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固定化可防止酶被血浆介导失活。

Immobilization protects enzymes from plasma-mediated inactivation.

机构信息

Applied Microbiology, Faculty of Biology and Biotechnology, Ruhr University Bochum, Bochum, Germany.

National Innovation Center for Synthetic Biotechnology, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, 32 West 7th Avenue, Tianjin Airport Economic Area, Tianjin 300308, People's Republic of China.

出版信息

J R Soc Interface. 2023 Oct;20(207):20230299. doi: 10.1098/rsif.2023.0299. Epub 2023 Oct 25.

Abstract

Non-thermal plasmas are used in various applications to inactivate biological agents or biomolecules. A complex cocktail of reactive species, (vacuum) UV radiation and in some cases exposure to an electric field together cause the detrimental effects. In contrast to this disruptive property of technical plasmas, we have shown previously that it is possible to use non-thermal plasma-generated species such as HO as cosubstrates in biocatalytic reactions. One of the main limitations in plasma-driven biocatalysis is the relatively short enzyme lifetime under plasma-operating conditions. This challenge could be overcome by immobilizing the enzymes on inert carrier materials. Here, we tested whether immobilization is suited to protect proteins from inactivation by plasma. To this end, using a dielectric barrier discharge device (PlasmaDerm), plasma stability was tested for five enzymes immobilized on ten different carrier materials. A comparative analysis of the treatment times needed to reduce enzyme activity of immobilized and free enzyme by 30% showed a maximum increase by a factor of 44. Covalent immobilization on a partly hydrophobic carrier surface proved most effective. We conclude from the study, that immobilization universally protects enzymes under plasma-operating conditions, paving the way for new emerging applications.

摘要

非热等离子体在各种应用中被用于灭活生物制剂或生物分子。活性物质的复杂混合物(真空)紫外线辐射,在某些情况下暴露于电场,共同导致有害影响。与技术等离子体的这种破坏性特性相反,我们之前已经表明,使用非热等离子体产生的物质,如 HO,可以作为生物催化反应的共底物。在等离子体驱动的生物催化中,主要的限制之一是在等离子体操作条件下酶的寿命相对较短。通过将酶固定在惰性载体材料上,可以克服这一挑战。在这里,我们测试了固定化是否适合保护蛋白质免受等离子体失活。为此,使用介电阻挡放电装置(PlasmaDerm),测试了五种固定在十种不同载体材料上的酶的等离子体稳定性。对固定化酶和游离酶的酶活性降低 30%所需的处理时间进行比较分析表明,最大增加了 44 倍。部分疏水性载体表面的共价固定化被证明最有效。我们从这项研究中得出结论,固定化普遍保护酶在等离子体操作条件下,为新的新兴应用铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/732c/10598437/edfe30dde334/rsif20230299f01.jpg

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