Abstract

Microbial communities associated with corals are an important source of bioactive metabolites with great potential for drug discovery. However, culturing these symbiotic microbes is extremely complex and often impossible. In toto coral aquaculture performed ex situ (the culture of the holobiont–cnidarian host and associated microorganisms) has been suggested as a potential solution to solve the constraints of supplying metabolite biomass to fuel the drug discovery pipeline. In the present study we investigated if coral fragmentation and different light intensities (photosynthetically active radiation (PAR) of 50, 80 and 120μmolquantam−2s−1) significantly affect the diversity and structure of the microbial communities present in the leather coral Sarcophyton cf. glaucum assessed through polymerase chain reaction denaturing gradient gel electrophoresis (PCR-DGGE). The diversity and structure of the bacterial communities present in mother colonies and fragments stocked under identical conditions remained stable two months post fragmentation, as well as between coral fragments stocked under different PAR intensities. The observed stability in the microbial community supports that in toto coral aquaculture may be a suitable option to produce metabolite biomass from symbiotic microorganisms. The possibility to employ a low PAR intensity to grow coral fragments without significantly affecting their microbial diversity and structure is likely to decrease aquaculture production costs and improve its economic viability.

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