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[Biosynthesis of calcifediol and calcitriol: a review].

Authors :
Ai J
Gao J
Yin Z
Mao S
Source :
Sheng wu gong cheng xue bao = Chinese journal of biotechnology [Sheng Wu Gong Cheng Xue Bao] 2024 Jun 25; Vol. 40 (6), pp. 1601-1619.
Publication Year :
2024

Abstract

VD <subscript>3</subscript> is a crucial vitamin for human health, as it enhances calcium absorption in the intestines and prevent rickets. Calcifediol (25(OH)VD <subscript>3</subscript> ) and calcitriol (1α,25(OH) <subscript>2</subscript> VD <subscript>3</subscript> ) are two derivatives of vitamin D <subscript>3</subscript> that play an important role in preventing and treating osteoporosis, as well as regulating human physiological functions. Currently, the production of calcifediol, and calcitriol primarily relies on chemical synthesis, which has disadvantages such as low product yield, numerous by-products, and environmental unfriendliness. Therefore, developing a green, safe, and environmentally friendly biocatalytic synthesis pathway is of utmost importance. This article mainly reviews the biocatalytic synthesis pathways of calcifediol, and calcitriol. The P450 enzymes, including P450 monooxygenases (cytochrome P450 monooxygenases, CYPs) and P450 peroxygenases (unspecific peroxygenases, UPOs), are crucial for the production of calcifediol and calcitriol. The catalytic mechanism of the extensively studied P450 monooxygenases, the selection of suitable redox partners, and the key residues involved in the enzyme's catalytic activity are analyzed. In addition, the review explores H <subscript>2</subscript> O <subscript>2</subscript> -driven UPOs, including their catalytic mechanism, strategies for high heterologous expression, and in situ regeneration of H <subscript>2</subscript> O <subscript>2</subscript> . UPOs are regarded as highly promising biocatalysts because they can facilitate reactions without the need for expensive cofactors and redox partners. This review offers insights into the engineering of P450 for the efficient production of vitamin D <subscript>3</subscript> derivatives.

Details

Language :
Chinese
ISSN :
1872-2075
Volume :
40
Issue :
6
Database :
MEDLINE
Journal :
Sheng wu gong cheng xue bao = Chinese journal of biotechnology
Publication Type :
Academic Journal
Accession number :
38914482
Full Text :
https://doi.org/10.13345/j.cjb.230664