Marine bacteria produce natural pigments; however, the ability of marine bacterial symbionts to produce natural pigments has been less studied. Marine bacteria associated with soft-coral Sarcophyton sp. collected from Karimunjawa Island were successfully isolated and screened to synthesize the carotenoid pigments. This approach has allowed the use of these symbionts as an environmental friendly source of new natural pigments. Out of 33 bacterial isolates, only 4 bacterial symbionts (CBSCP 2-2, CBSCP 2-3, CBSCP 1-1, and CBSCP 2-4), positively contain carotenoid pigments. Molecular identification based on 16S rDNA method showed that bacterial symbionts CBSCP 2-2, CBSCP 2-3, CBSCP 1-1, and CBSCP 2-4 were closely related to Pseudoalteromonas shioyasakiensis, Pseudoalteromonas rubra, Virgibacillus salaries, and Pseudoalteromonas spongiae. Pigment analysis showed that the pigments have been categorized within the groups of carotenoid pigments. Antioxidant activity of pigment extracts was done by measuring inhibitory concentration (IC 50 ) of pigment extract against 2,2-diphenyl-1-picrylhydrazyl (DPPH) solution. The antioxidant activity measurement of CBSCP 1-1, CBSCP 2-2, CBSCP 2-3, and CBSCP 2-4 extract, and b-carotene was 2015, 5017, 2520, 4213, and 1980 mg l -1 , respectively.
Sponge-associated fungi are attractive targets for the isolation of bioactive natural products with different pharmaceutical purposes. In this investigation, 20 fungi were isolated from 10 different sponge specimens. One isolate, the fungus Penicillium citrinum strain WK-P9, showed activity against Bacillus subtilis JH642 when cultivated in malt extract medium. One new and three known citrinin derivatives were isolated from the extract of this fungus. The structures were elucidated by 1D and 2D NMR spectroscopy, as well as LC-HRMS. Their antibacterial activity against a set of common human pathogenic bacteria and fungi was tested. Compound 2 showed moderate activity against Mycobacterium smegmatis ATCC607 with a minimum inhibitory concentration (MIC) of 32 µg/mL. Compound 4 exhibited moderate growth inhibition against Bacillus subtilis JH642, B. megaterium DSM32, and M. smegmatis ATCC607 with MICs of 16, 16, and 32 µg/mL, respectively. Furthermore, weak activities of 64 µg/mL against B. subtilis DSM10 and S. aureus ATCC25923 were observed for compound 4.
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