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Harvesting of sponges is not an option for the production of biomedical substances. Neither are synthetic production or lab cultivation of bio-active components viable options. According to a couple of researches, isolating sponge cells and
growing them in a bio-reactor under optimal conditions has the best
chance of being successful. However, sponges are notoriously difficult to identify and any cell line needs to start with a properly identified donor organism.
The Sponge Barcoding Project started a couple of years ago with the aim to cover all sponge taxa, and ranging in
habitat from the marine intertidal to the deep-sea, as well as
freshwater. The Sponge Barcoding Project was a major partner of the Marine Barcode of Life project (MarBOL). The goal was to obtain DNA Barcodes from 8,000 taxa to
provide a basis from which more extensive sampling would be directed and routine identifications enabled.
Recently described type specimens curated in associated museums were targeted first and will be supplemented with unequivocally identifiable taxa.
Sponge Barcoding isn't as easy and as straightforward as one would hope. They host a large number
of non-target macro- and microorganisms found in association with them.
The DNA of these organisms can be co-extracted, and either co-amplified
or preferentially amplified during PCR causing sequences to be
difficult to read or belonging to non-target organisms. Moreover, for
defense purposes, sponges produce potent bioactive compounds that can
inhibit enzymatic reactions such as PCR. Another issue stems from the fact that some sponges show only very little or no variation in the standard COI region which led to developments of protocols that allow us to obtain longer sequences that contain sufficient variation. Often DNA barcodes are supplemented with ITS to enable unambiguous identifications.
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