4.7 Article

Anaerobic biosynthesis of rhamnolipids by Pseudomonas aeruginosa: performance, mechanism and its application potential for enhanced oil recovery

期刊

MICROBIAL CELL FACTORIES
卷 20, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12934-021-01593-4

关键词

Pseudomonas aeruginosa; Rhamnolipids; Anaerobic biosynthesis; Glycerol; RmlBDAC; Microbial enhanced oil recovery

资金

  1. National Natural Science Foundation of China [31700117]
  2. Introduced Talent Research Start-up Fund of Qufu Normal University
  3. Young Talents Invitation Program of Shandong Provincial Colleges and Universities

向作者/读者索取更多资源

Pseudomonas aeruginosa SG can anaerobically produce rhamnolipids using glycerol as carbon source, with key genes showing significantly up-regulated expression. The anaerobic biosynthetic pathway of rhamnolipids in P. aeruginosa SG involves gluconeogenesis from glycerol, biosynthesis of dTDP-l-rhamnose and beta-hydroxy fatty acids, and rhamnosyl transfer process.
Background Pseudomonas aeruginosa, the rhamnolipids-producer, is one of dominant bacteria in oil reservoirs. Although P. aeruginosa strains are facultative bacteria, the anaerobic biosynthesis mechanism of rhamnolipids is unclear. Considering the oxygen scarcity within oil reservoirs, revealing the anaerobic biosynthesis mechanism of rhamnolipids are significant for improving the in-situ production of rhamnolipids in oil reservoirs to enhance oil recovery. Results Pseudomonasaeruginosa SG anaerobically produced rhamnolipids using glycerol rather than glucose as carbon sources. Two possible hypotheses on anaerobic biosynthesis of rhamnolipids were proposed, the new anaerobic biosynthetic pathway (hypothesis 1) and the highly anaerobic expression of key genes (hypothesis 2). Knockout strain SG Delta rmlB failed to anaerobically produce rhamnolipids using glycerol. Comparative transcriptomics analysis results revealed that glucose inhibited the anaerobic expression of genes rmlBDAC, fabABG, rhlABRI, rhlC and lasI. Using glycerol as carbon source, the anaerobic expression of key genes in P. aeruginosa SG was significantly up-regulated. The anaerobic biosynthetic pathway of rhamnolipids in P. aeruginosa SG were confirmed, involving the gluconeogenesis from glycerol, the biosynthesis of dTDP-l-rhamnose and beta-hydroxy fatty acids, and the rhamnosyl transfer process. The engineered strain P. aeruginosa PrhlAB constructed in previous work enhanced 9.67% of oil recovery higher than the wild-type strain P. aeruginosa SG enhancing 8.33% of oil recovery. Conclusion The highly anaerobic expression of key genes enables P. aeruginosa SG to anaerobically biosynthesize rhamnolipids. The genes, rmlBDAC, fabABG, rhlABRI, rhlC and lasI, are key genes for anaerobic biosynthesis of rhamnolipid by P. aeruginosa. Improving the anaerobic production of rhamnolipids better enhanced oil recovery in core flooding test. This study fills the gaps in the anaerobic biosynthesis mechanism of rhamnolipids. Results are significant for the metabolic engineering of P. aeruginosa to enhance anaerobic production of rhamnolipids.

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