AI Article Synopsis

  • - The soil bacterium Pseudomonas putida KT2440 shows notable ability to tolerate various toxic chemicals, outperforming Escherichia coli in its ability to withstand three of eleven tested compounds, including p-coumaric acid, which has significant industrial applications.
  • - Researchers used a genome-wide method called Tn-seq to explore how P. putida KT2440 tolerates p-coumaric acid, analyzing a large set of mutant strains to see which were more or less successful in the presence of this compound.
  • - Key findings revealed that several genes, particularly the ABC transporter Ttg2ABC and components of the cytochrome c maturation system, are crucial for maintaining membrane stability and transport processes, linking

Article Abstract

The soil bacterium Pseudomonas putida KT2440 has gained increasing biotechnological interest due to its ability to tolerate different types of stress. Here, the tolerance of P. putida KT2440 toward eleven toxic chemical compounds was investigated. P. putida was found to be significantly more tolerant toward three of the eleven compounds when compared to Escherichia coli. Increased tolerance was for example found toward p-coumaric acid, an interesting precursor for polymerization with a significant industrial relevance. The tolerance mechanism was therefore investigated using the genome-wide approach, Tn-seq. Libraries containing a large number of miniTn5-Km transposon insertion mutants were grown in the presence and absence of p-coumaric acid, and the enrichment or depletion of mutants was quantified by high-throughput sequencing. Several genes, including the ABC transporter Ttg2ABC and the cytochrome c maturation system (ccm), were identified to play an important role in the tolerance toward p-coumaric acid of this bacterium. Most of the identified genes were involved in membrane stability, suggesting that tolerance toward p-coumaric acid is related to transport and membrane integrity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814926PMC
http://dx.doi.org/10.1002/bit.26495DOI Listing

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