Development of metabolic pathways for the biosynthesis of hydroxyacids and lactones

[摘要] (cont.) Supplying glucose to E. coli expressing these enzymes resulted in 3HB production, while supplying glucose and propionate results in 3HV production. Supplying glucose and glycolate resulted in DHBA production with some 3-HBL, but only with the help of a fourth gene - propionyl-CoA transferase (pct). Removing the tesB gene from this four-gene system substantially increases 3-HBL titers at the expense of DHBA. This work represents the first successful production of DHBA and 3-HBL in a biological system from carbohydrate-based substrates. In each of these systems, several broadly-applicable tools and strategies were developed to enhance product titer or discover new metabolic activities. In the P. putida system, cytosolic and extracytosolic biocatalysis were combined in a single metabolic pathway to realize lactone production. This catalytic strategy, termed integrated bioprocessing, is applicable to other metabolic pathways whose production suffers due to a suboptimal cytosolic enzyme. Also in the P. putida system, two-phase cultures were used to sequester the lactone product away from the lactonase, helping to drive lactonehydroxyacid equilibrium towards the lactone. This methodology allows one to overcome equilibrium-based limitations of product titer. Finally in the E. coli work, a promiscuous pathway normally used for polyhydroxyalkanoate synthesis was exploited to give a wide range of hydroxyacid products. This substrate promiscuity was critical in achieving the production of new compounds biologically and thus substrate promiscuity was identified as a key component for metabolic pathway design and construction.

[发布机构] Massachusetts Institute of Technology