Systems-level analysis of 1,6-hexanediol stress response and tolerance engineering in Escherichia coli
TL;DR
This study demonstrates that 1,6-HDO exhibited strong inhibitory effects on Escherichia coli, reducing the maximum OD600 to approximately 50% of the control level under 10 g/L stress and identifies key determinants contributing to tolerance.
Abstract
1,6-Hexanediol (1,6-HDO) is an important chemical platform widely used in polymer and pharmaceutical industries, while its toxicity remains a major bottleneck limiting efficient microbial production. This study demonstrates that 1,6-HDO exhibited strong inhibitory effects on Escherichia coli, reducing the maximum OD600 to approximately 50% of the control level under 10 g/L stress. Transcriptomic analysis was performed under 1,6-HDO stress, identifying 779 differentially expressed genes enriched in pathways related to energy metabolism, sulfur metabolism and amino acid metabolism. To systematically identify functional targets associated with tolerance, genome-wide screening using the ASKA overexpression library identified 93 tolerance-related genes that improved E. coli growth under 1,6-HDO stress by 0.06- to 3.17-fold. Notably, multiple targets were functionally associated with energy and amino acid metabolism, consistent with the transcriptomic analysis. Furthermore, co-expression of rumA and yhbO showed the greatest improvement in growth, reaching a biomass of 9.43 under 1,6-HDO stress, which was 2.61-fold higher than that of the control strain. Collectively, this study systematically elucidates the global stress response and identifies key determinants contributing to tolerance, providing valuable targets for developing robust microbial cell factories for efficient 1,6-HDO bioproduction.