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使用表达青霉素V酰基转移酶的Lentikats封装细胞生产6-氨基青霉烷酸的工艺开发

Process Development for 6-Aminopenicillanic Acid Production Using Lentikats-Encapsulated Cells Expressing Penicillin V Acylase.

作者信息

Sawant Amol M, Sunder Avinash Vellore, Vamkudoth Koteswara Rao, Ramasamy Sureshkumar, Pundle Archana

机构信息

Biochemical Sciences Division, National Chemical Laboratory-CSIR, Pune 411008, India.

Academy of Scientific and Innovative Research (AcSIR), New Delhi 110001, India.

出版信息

ACS Omega. 2020 Nov 6;5(45):28972-28976. doi: 10.1021/acsomega.0c02813. eCollection 2020 Nov 17.

DOI:10.1021/acsomega.0c02813
PMID:33225127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7675567/
Abstract

Penicillin V acylase (PVA, EC 3.5.1.11) hydrolyzes the side chain of phenoxymethylpenicillin (Pen V) and finds application in the manufacture of the pharmaceutical intermediate 6-aminopenicillanic acid (6-APA). Here, we report the scale-up of cultivation of whole cells expressing a highly active PVA from and their encapsulation in polyvinyl alcohol-poly(ethylene glycol) Lentikats hydrogels. A biocatalytic process for the hydrolysis of 2% (w/v) Pen V was set up in a 2 L reactor using the Lentikats-immobilized whole cells, with a customized setup to enable continuous downstream processing of the reaction products. The biocatalytic reaction afforded complete conversion of Pen V for 10 reaction cycles, with an overall 90% conversion up to 50 cycles. The bioprocess was further scaled up to the pilot-scale at 10 L, enabling complete conversion of Pen V to 6-APA for 10 cycles. The 6-APA and phenoxy acetic acid products were recovered from downstream processing with isolated yields of 85-90 and 87-92%, respectively. Immobilization in Lentikats beads improved the stability of the whole cells on storage, maintaining 90-100% activity and similar conversion efficiency after 3 months at 4 °C. The robust PVA biocatalyst can be employed in a continuous process to provide a sustainable route for bulk 6-APA production from Pen V.

摘要

青霉素V酰基转移酶(PVA,EC 3.5.1.11)可水解苯氧甲基青霉素(青霉素V)的侧链,并应用于药物中间体6-氨基青霉烷酸(6-APA)的生产。在此,我们报道了表达高活性PVA的全细胞培养的放大过程以及将其包封在聚乙烯醇-聚(乙二醇)Lentikats水凝胶中的过程。使用Lentikats固定化全细胞在2 L反应器中建立了用于水解2%(w/v)青霉素V的生物催化过程,并采用定制装置实现反应产物的连续下游处理。该生物催化反应在10个反应循环中实现了青霉素V的完全转化,在50个循环内总转化率达到90%。该生物过程进一步放大至10 L中试规模,在10个循环中实现了青霉素V向6-APA的完全转化。从下游处理中回收的6-APA和苯氧乙酸产物的分离产率分别为85-90%和87-92%。固定在Lentikats珠中提高了全细胞储存时的稳定性,在4℃下放置3个月后仍保持90-100%的活性和相似的转化效率。这种强大的PVA生物催化剂可用于连续过程,为从青霉素V大规模生产6-APA提供一条可持续的途径。

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