Abstract
AbstractEscherichia coliare model organisms for biotechnological research owing to their abilities to grow on defined media and consume a variety of carbon sources, as well as a vast knowledge base and tools available for their manipulation. SeveralE. colistrains and their derivatives are available. However, the quantitative metabolic differences between the strains could be better characterized. In this study, we investigated the differences in the intracellular flux distribution between three commonly used strains ofE. coli(K-12 MG1655, C, and W) using13C-Metabolic flux analysis (13C-MFA), the gold standard in fluxomics. The labeling data was analyzed using FluxPyt, our previously developed Python-based tool. Threefold differences in the growth rates of these strains were observed when growing anaerobically on glucose in M9 medium, withE. coliW being the fastest (μ = 0.62 ± 0.01 h-1) andE. coliC the slowest (μ = 0.22 ± 0.01 h-1). The strain’s growth rates correlate with glucose uptake and flux through the oxidative pentose phosphate pathway. Interestingly, succinate was a major product inE. coliC only.13C-MFA revealed that under these conditions, Entner–Doudoroff (ED) pathway was active inE. coliC andE. coliW but not inE. coliK-12 MG1655. InE. coliK-12 MG1655 andE. coliC, the Tricarboxylic Acid (TCA) cycle ran incompletely. Also, the glyoxylate shunt was inactive in all three strains. Growth, xylose intake rates, and product profiles on xylose mirrored those of glucose. Thus, this study has highlighted significant differences in the growth and metabolism of theE. colistrains on glucose and xylose. This will form a basis for identifying the best strain for a particular application.
Publisher
Cold Spring Harbor Laboratory