AI Article Synopsis

  • The Alteromonas stellipolaris strains PQQ-42 and PQQ-44, isolated from a fish hatchery, exhibit strong quorum quenching activity and can decrease Vibrio-induced mortality in corals.
  • Both strains possess genes that allow them to degrade AHL quorum sensing signals, with PQQ-42 producing more exopolysaccharides (EPS) than PQQ-44, which contains fucose that has potential biotechnological applications.
  • Genome analysis revealed the presence of a new NRPS cluster in PQQ-42, signifying the potential for both strains to synthesize valuable bioactive compounds.

Article Abstract

The Alteromonas stellipolaris strains PQQ-42 and PQQ-44, previously isolated from a fish hatchery, have been selected on the basis of their strong quorum quenching (QQ) activity, as well as their ability to reduce Vibrio-induced mortality on the coral Oculina patagonica. In this study, the genome sequences of both strains were determined and analyzed in order to identify the mechanism responsible for QQ activity. Both PQQ-42 and PQQ-44 were found to degrade a wide range of N-acylhomoserine lactone (AHL) QS signals, possibly due to the presence of an aac gene which encodes an AHL amidohydrolase. In addition, the different colony morphologies exhibited by the strains could be related to the differences observed in genes encoding cell wall biosynthesis and exopolysaccharide (EPS) production. The PQQ-42 strain produces more EPS (0.36 g l) than the PQQ-44 strain (0.15 g l), whose chemical compositions also differ. Remarkably, PQQ-44 EPS contains large amounts of fucose, a sugar used in high-value biotechnological applications. Furthermore, the genome of strain PQQ-42 contained a large non-ribosomal peptide synthase (NRPS) cluster with a previously unknown genetic structure. The synthesis of enzymes and other bioactive compounds were also identified, indicating that PQQ-42 and PQQ-44 could have biotechnological applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361997PMC
http://dx.doi.org/10.1038/s41598-018-37720-2DOI Listing

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