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利用咖啡渣和茶叶残渣产生的过氧化氢进行过氧合酶催化氧化反应的可持续方法。

Sustainable Approach for Peroxygenase-Catalyzed Oxidation Reactions Using Hydrogen Peroxide Generated from Spent Coffee Grounds and Tea Leaf Residues.

作者信息

Kawana Hideaki, Miwa Toru, Honda Yuki, Furuya Toshiki

机构信息

Faculty of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda 278-8510, Chiba, Japan.

Department of Chemistry, Biology, and Environmental Science, Faculty of Science, Nara Women's University, Kitauoyanishi-machi, Nara 630-8506, Japan.

出版信息

ACS Omega. 2022 Jun 1;7(23):20259-20266. doi: 10.1021/acsomega.2c02186. eCollection 2022 Jun 14.

DOI:10.1021/acsomega.2c02186
PMID:35721909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9201881/
Abstract

Peroxygenases are promising catalysts for use in the oxidation of chemicals as they catalyze the direct oxidation of a variety of compounds under ambient conditions using hydrogen peroxide (HO) as an oxidant. Although the use of peroxygenases provides a simple method for oxidation of chemicals, the anthraquinone process currently used to produce HO requires significant energy input and generates considerable waste, which negatively affects process sustainability and production costs. Thus, generating HO for peroxygenases on site using an environmentally benign method would be advantageous. Here, we utilized spent coffee grounds (SCGs) and tea leaf residues (TLRs) for the production of HO. These waste biomass products reacted with molecular oxygen and effectively generated HO in sodium phosphate buffer. The resulting HO was utilized by the bacterial P450 peroxygenase, CYP152A1. Both SCG-derived and TLR-derived HO promoted the CYP152A1-catalyzed oxidation of 4-methoxy-1-naphthol to Russig's blue as a model reaction. In addition, when CYP152A1 was incubated with styrene, the SCG and TLR solutions enabled the synthesis of styrene oxide and phenylacetaldehyde. This new approach using waste biomass provides a simple, cost-effective, and sustainable oxidation method that should be readily applicable to other peroxygenases for the synthesis of a variety of valuable chemicals.

摘要

过氧化酶是用于化学物质氧化的有前景的催化剂,因为它们在环境条件下使用过氧化氢(HO)作为氧化剂催化多种化合物的直接氧化。尽管使用过氧化酶为化学物质氧化提供了一种简单方法,但目前用于生产HO的蒽醌工艺需要大量能量输入并产生大量废物,这对工艺可持续性和生产成本产生负面影响。因此,使用环境友好的方法现场为过氧化酶生成HO将是有利的。在这里,我们利用废弃咖啡渣(SCG)和茶叶残渣(TLR)来生产HO。这些废弃生物质产品与分子氧反应,并在磷酸钠缓冲液中有效地生成HO。生成的HO被细菌P450过氧化酶CYP152A1利用。以SCG衍生的HO和TLR衍生的HO都促进了CYP152A1催化4-甲氧基-1-萘酚氧化为吕西格蓝作为模型反应。此外,当CYP152A1与苯乙烯一起孵育时,SCG和TLR溶液能够合成环氧苯乙烷和苯乙醛。这种使用废弃生物质的新方法提供了一种简单、经济高效且可持续的氧化方法,应该很容易应用于其他过氧化酶以合成各种有价值的化学品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/314d4a20b1c8/ao2c02186_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/56dd08046791/ao2c02186_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/1a300bd0e07a/ao2c02186_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/212d3206a0a2/ao2c02186_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/bbbe83ab6095/ao2c02186_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/314d4a20b1c8/ao2c02186_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/56dd08046791/ao2c02186_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/1a300bd0e07a/ao2c02186_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/212d3206a0a2/ao2c02186_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/bbbe83ab6095/ao2c02186_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bc3/9201881/314d4a20b1c8/ao2c02186_0005.jpg

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