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Updated: Sep 19, 2025

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Highly Efficient One-Pot Multienzyme Cascades for the Synthesis of S-Allyl-l-Cysteine from l-Serine and Allyl
Gang Zhu1, Chenchen Zhang1, Yunjie Xiao2
1Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin Key Laboratory of Industrial Microbiology, College of Biotechnology, Tianjin University of Science and Technology, Tianjin 300457, P. R. China.
Abstract:
S-Allyl-l-cysteine (SAC) is an important bioactive substance in garlic, which has potential preventive and therapeutic effects, including antioxidant, anticancer, hepatoprotective, and neuroprotective properties. Here, a promising in vitro multienzyme cascade catalysis system comprising serine acetyltransferase (SAT) and O-acetylserine sulfhydrylase B (OASS B) was established using l-serine and allyl mercaptan as substrates for the efficient synthesis of SAC. Three SAT mutants (SATT167A, SATM201R, and SATN264X) were designed to weaken the feedback inhibitory effect of SAC on SAT activity, with one SATM201R mutant achieving a SAC yield of 75.5%. Furthermore, by coupling an acetyl-CoA regeneration system, we improved the synthetic yield of the SAC cascade catalytic system to 76.9%, enabling a cost-effective and efficient one-pot enzymatic synthesis of SAC in vitro. This study provides an alternative economical and environmentally sustainable biosynthetic pathway for the efficient production of SAC.
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