In the course of our screening program, the EtOAc extract of a Micromonospora sp. (strain G044) from sponge Tethya aurantium of the sea of Côtô -Thanh Lân exhibited antimicrobial activity against Enterococcus faecalis, Bacillus cereus and Candida albicans. In this paper, we reported the isolation and structural elucidation of six secondary metabolites Cyclo-(Pro-Trp) (1), Cyclo-(Pro-Met) (2), Cyclo-(Pro-Val) (4), N-acetyltryptamine (3), uridine (5), and 2-phenylacetic acid (6) from the cultures broth of Micromonospora sp. (strain G044). The structures of 1 -6 were determined by analyses of MS and 2D NMR data. All compounds were evaluated for their antimicrobial activity against a panel of clinically significant microorganisms. Compound 1 inhibited Escherichia coli with a MIC value of 128 µg/ml.

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The discovery of bioactive compounds from marine microorganisms for drug development has been currently widely studied. In which marine actinomycetes are highlighted as a potential source in finding antibiotics as well as substances with biological activity in general. The objective of this study is to isolate and screen the actinomycetes strains with antibacterial activity from the marine environment. Sixty one actinomycetes were isolated from 80 samples of marine organisms and sediments collected from Ly Son Island, Quang Ngai. The strains were fermented in the A1 medium and the culture broths were extracted by ethyl acetate and vacuum rotary evaporation to produce crude extracts. Antimicrobial activity of the extracts were carried out on 7 strains of tested microorganisms, including three strains of Gram-negative bacteria (Escherichia coli ATCC25922, Pseudomonas aeruginosa ATCC27853, Salmonella enterica ATCC13076), three Gram-positive strains (Enterococcus faecalis ATCC29212, Staphylococus aureus ATCC25923, Bacillus cereus ATCC 13245), and yeast Candida albicans ATCC10231. The screening results showed that three strains with the highest antimicrobial activity (G330, G336 and G361) were capable of inhibiting 5 of the 7 tested microorganisms with Minimum Inhibitory Concentration (MIC) values ranging from 4 to 256 μg/mL, depending on each tested strain. Specifically, all three strains inhibited C. albicans ATCC10231 and three Gram-positive strains (E. faecalis ATCC29212, S. aureus ATCC25923, B. cereus ATCC 13245). In addition, G330 and G336 also showed the inhibitory activity to Gram negative strain S. enterica ATCC13076 with value of 256 µg/mL, G361 has a good inhibitory ability for E. coli ATCC25922 with MIC value of 8 µg/mL. The strains were identified by morphological and the 16S rRNA gene sequences. The results showed that 16S rRNA sequences of the strains had over 99% similarity to the 16S rRNA sequences on the GeneBank database, strains G336 and G361 belonged to the genus Salinispora, whereas strain G330 belonged to the genus Streptomyces. These results showed that marine environment has a great potential in solation of actinomycetes strains for the search for antibacterial substances as well as other biologically active compounds.

Chromatographic separation of ethyl acetate extract of the stingless bee Lisotrigona furva propolis, that collected in Khanh Hoa province, led to isolation of five cycloartane‐type triterpenes including cycloartenone (1), cycloartenol (2), (24E)‐3β‐hydroxycycloart‐24‐en‐26‐al (3), mangiferonic acid (4) and mangiferolic acid (5). Mango plant (Mangifera indica) was suggested to be a resin source of the propolis. The propolis EtOH extract showed good antimicrobial activity on Gram (+) strain E. feacalis and fungus C. albicans. Among the isolated compounds, compound 3 displayed selective activity against three Gram (+) strains and C. albicans over Gram (‐) strains with all MIC values of 64 μg/mL. However, the propolis EtOH extract was not active against LU‐1 and MCF‐7 cancer cell lines. Only compound 5 exhibited moderate activity on LU‐1 cancer cell line with IC50 of 13.33 μg/mL.