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Auteurs principaux: Feng, Dandan, Zhang, Tianshu, Zhou, Guan, Cao, Yanli, Luo, Quan, Xu, Huifang, Lu, Xuefeng
Format: Artículo científico
Langue:en
Publié: Synthetic and systems biotechnology 2026
Accès en ligne:https://pubmed.ncbi.nlm.nih.gov/42179739/
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author Feng, Dandan
Zhang, Tianshu
Zhou, Guan
Cao, Yanli
Luo, Quan
Xu, Huifang
Lu, Xuefeng
author_facet Feng, Dandan
Zhang, Tianshu
Zhou, Guan
Cao, Yanli
Luo, Quan
Xu, Huifang
Lu, Xuefeng
Feng, Dandan
Zhang, Tianshu
Zhou, Guan
Cao, Yanli
Luo, Quan
Xu, Huifang
Lu, Xuefeng
collection PubMed - marine biology
contents Efficient whole-cell biocatalytic synthesis of 2'-deoxy-2'-fluoroadenosine, a key building block for nucleic acid drugs. Feng, Dandan Zhang, Tianshu Zhou, Guan Cao, Yanli Luo, Quan Xu, Huifang Lu, Xuefeng 2'-Deoxy-2'-fluoroadenosine (2'-F-dA) is a nucleoside analogue used as a key building block for oligonucleotide drugs. It can be biosynthesized from a low-cost 2'-deoxy-2'-fluorouridine via one-pot transglycosylation catalyzed by a thymidine phosphorylase (TP) and a purine nucleoside phosphorylase (PNP). However, reliance on purified enzymes and low space-time yields present challenges for industrial application of the process. Here, we develop a whole-cell-based biocatalytic system employing TP and PNP from , which demonstrates high catalytic efficiency and operational simplicity in scaled-up reaction. In particular, a thermal pretreatment of TP- and PNP-expressing whole cells, determined as 50 °C for 3 h, effectively suppressed endogenous deamination side reaction while enhancing 2'-F-dA yield. Subsequent optimization of enzyme and substrate loadings and their relative ratios achieved an unprecedented space-time yield of 1.22 g/L/h with 88.1 g/L product titer in a 500 mL scaled-up reaction, manifesting a highest total conversion of 68.2 %. An integrated purification process yielded gram-scale solid powder of 2'-F-dA with 98.0 % chemical purity and 85.0 % recovery. This novel whole-cell biocatalytic process demonstrates significant industrial potential for the production of 2'-F-dA.
format Artículo científico
id pubmed_42179739
institution PubMed
language en
publishDate 2026
publisher Synthetic and systems biotechnology
record_format pubmed
spellingShingle Efficient whole-cell biocatalytic synthesis of 2'-deoxy-2'-fluoroadenosine, a key building block for nucleic acid drugs.
Feng, Dandan
Zhang, Tianshu
Zhou, Guan
Cao, Yanli
Luo, Quan
Xu, Huifang
Lu, Xuefeng
Efficient whole-cell biocatalytic synthesis of 2'-deoxy-2'-fluoroadenosine, a key building block for nucleic acid drugs. Feng, Dandan Zhang, Tianshu Zhou, Guan Cao, Yanli Luo, Quan Xu, Huifang Lu, Xuefeng 2'-Deoxy-2'-fluoroadenosine (2'-F-dA) is a nucleoside analogue used as a key building block for oligonucleotide drugs. It can be biosynthesized from a low-cost 2'-deoxy-2'-fluorouridine via one-pot transglycosylation catalyzed by a thymidine phosphorylase (TP) and a purine nucleoside phosphorylase (PNP). However, reliance on purified enzymes and low space-time yields present challenges for industrial application of the process. Here, we develop a whole-cell-based biocatalytic system employing TP and PNP from , which demonstrates high catalytic efficiency and operational simplicity in scaled-up reaction. In particular, a thermal pretreatment of TP- and PNP-expressing whole cells, determined as 50 °C for 3 h, effectively suppressed endogenous deamination side reaction while enhancing 2'-F-dA yield. Subsequent optimization of enzyme and substrate loadings and their relative ratios achieved an unprecedented space-time yield of 1.22 g/L/h with 88.1 g/L product titer in a 500 mL scaled-up reaction, manifesting a highest total conversion of 68.2 %. An integrated purification process yielded gram-scale solid powder of 2'-F-dA with 98.0 % chemical purity and 85.0 % recovery. This novel whole-cell biocatalytic process demonstrates significant industrial potential for the production of 2'-F-dA.
title Efficient whole-cell biocatalytic synthesis of 2'-deoxy-2'-fluoroadenosine, a key building block for nucleic acid drugs.
url https://pubmed.ncbi.nlm.nih.gov/42179739/