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Free keywords:
auxin, CRISPR-Cas6, pathway flux, malate, substrate channeling, synthetic biology
Abstract:
Enzyme–enzyme assemblies commonly occur naturally, yet the factors that lead to their transient nature are not fully understood. Mitkas et al. have shown how clustered regularly interspaced short palindromic repeats (CRISPR) enzymes and RNA scaffolds allow synthetic enzyme complexes to be formed and disassembled as needed, providing powerful new tools for metabolic engineering.