Genome-wide mapping of furfural tolerance genes in Escherichia coli

PLoS One. 2014 Jan 28;9(1):e87540. doi: 10.1371/journal.pone.0087540. eCollection 2014.

Abstract

Advances in genomics have improved the ability to map complex genotype-to-phenotype relationships, like those required for engineering chemical tolerance. Here, we have applied the multiSCale Analysis of Library Enrichments (SCALEs; Lynch et al. (2007) Nat. Method.) approach to map, in parallel, the effect of increased dosage for >10(5) different fragments of the Escherichia coli genome onto furfural tolerance (furfural is a key toxin of lignocellulosic hydrolysate). Only 268 of >4,000 E. coli genes (∼ 6%) were enriched after growth selections in the presence of furfural. Several of the enriched genes were cloned and tested individually for their effect on furfural tolerance. Overexpression of thyA, lpcA, or groESL individually increased growth in the presence of furfural. Overexpression of lpcA, but not groESL or thyA, resulted in increased furfural reduction rate, a previously identified mechanism underlying furfural tolerance. We additionally show that plasmid-based expression of functional LpcA or GroESL is required to confer furfural tolerance. This study identifies new furfural tolerant genes, which can be applied in future strain design efforts focused on the production of fuels and chemicals from lignocellulosic hydrolysate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping
  • Cloning, Molecular
  • DNA Mutational Analysis
  • Drug Resistance, Bacterial / genetics*
  • Escherichia coli / drug effects
  • Escherichia coli / genetics*
  • Escherichia coli Proteins / genetics
  • Furaldehyde / pharmacology*
  • Genetic Association Studies
  • Heat-Shock Proteins / genetics
  • Mutagens / pharmacology*

Substances

  • Escherichia coli Proteins
  • GroE protein, E coli
  • Heat-Shock Proteins
  • Mutagens
  • Furaldehyde

Grants and funding

This work was supported by the Department of Energy through subcontract no. ZCO-7-77431-001 to the National Renewable Energy Laboratory. This work was also supported by the National Science Foundation award number CBET 1067730. With the exception of study conception and roles consistent with authorship by MZ, the funding agencies had no role in the study design, data collection and analysis, or decision to publish. TYG and NRS were supported as National Science Foundation Graduate Research Fellowship Program recipients.