2026· American Journal of Medical and Clinical Research & Reviews· Vol 01, pp. 01-08· 0 citations
TL;DR
This study aims to expand cglPS26 into a multi-strain model, cglTY26, which contained 1109 metabolites, 511 enzymes and their corresponding transcription and translation processes, and 1195 enzymatic reactions and provides a useful toolkit for further refinement, experimental validation, and future applications in metabolic engineering.
Abstract
Corynebacterium glutamicum is an industrially important bacterium widely used in amino acid production. In metabolic engineering, metabolic models such as constraint-based genome scale models (GSMs) and kinetic models (KMs) can be useful computational tool guide the rational design of genetic modifications to optimize production of desired compounds in the microbe. Compared to GSMs which emphasis on steady-state flux distribution, KMs enable a comprehensive dynamic visualization of the metabolic network, by simulating the rate of change of metabolite concentration. A recent whole cell kinetic model of Corynebacterium glutamicum ATCC 13032, cglPS26, has been published. Hence, this study aims to expand cglPS26 into a multi-strain model, cglTY26, contained 1109 metabolites, 511 enzymes and their corresponding transcription and translation processes, and 1195 enzymatic reactions. This model provides a useful toolkit for further refinement, experimental validation, and future applications in metabolic engineering.
This review presents a comprehensive analysis of recent advances in microbial BCAAs production through a Mechanism-Module-Process framework, providing a holistic roadmap for constructing superior BCAAs cell factories and extending their metabolic potential toward derivative biosynthesis.
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