Chemical conversion of the extract of natural resources is a very attractive way to expand the chemical space to discover bioactive compounds. In order to search for new medicines to treat parasitic diseases that cause high morbidity and mortality in affected countries in the world, the ethyl acetate extract from the rhizome of Alpinia galanga (L.) has been chemically converted by epoxidation using dioxirane generated in situ. The biological activity of chemically converted extract (CCE) of A. galanga (L.) significantly increased the activity against Leishmania major up to 82.6 ± 6.2 % at 25 μg/mL (whereas 2.7 ± 0.8% for the original extract). By bioassay-guided fractionation, new phenylpropanoids (1–6) and four known compounds, hydroquinone (7), 4-hydroxy(4-hydroxyphenyl)methoxy)benzaldehyde (8), isocoumarin cis 4-hydroxymelein (9), and (2S,3S,6R,7R,9S,10S)-humulene triepoxide (10) were isolated from CCE. The structures of isolated compounds were determined by spectroscopic analyses of 1D and 2D NMR, IR, and MS spectra. The most active compound was hydroquinone (7) with IC50 = 0.37 ± 1.37 μg/mL as a substantial active principle of CCE. In addition, the new phenylpropanoid 2 (IC50 = 27.8 ± 0.34 μg/mL) also showed significant activity against L. major compared to the positive control miltefosine (IC50 = 7.47 ± 0.3 μg/mL). The activities of the isolated compounds were also evaluated against Plasmodium falciparum, Trypanosoma brucei gambisense and Trypanosoma brucei rhodeisense. Interestingly, compound 2 was selectively active against trypanosomes with potent activity. To the best of our knowledge, this is the first report on the bioactive “unnatural” natural products from the crude extract of A. galanga (L.) by chemical conversion and on its activities against causal pathogens of leishmaniasis, trypanosomiasis, and malaria.
In our continuing research for bioactive constituents from natural resources, a new methyl threonolactone glucopyranoside (1), a new methyl threonolactone fructofuranoside (2), 2 new pyroglutamates (3 and 4), and 10 known compounds (5–14) were isolated from the whole plant of Spilanthes acmella (L.) L. The structures of these compounds were determined based on various spectroscopic and chemical analyses. All of the isolated compounds were evaluated on bone formation parameters, such as ALP (alkaline phosphatase) and mineralization stimulatory activities of MC3T3-E1 cell lines. The results showed that the new compound, 1,3-butanediol 3-pyroglutamate (4), 2-deoxy-d-ribono-1,4-lactone (6), methyl pyroglutamate (7), ampelopsisionoside (10), icariside B1 (11), and benzyl α-l-arabinopyranosyl-(1→6)-β-d-glucopyranoside (12) stimulated both ALP and mineralization activities.
PhzM and PhzS are two “core” enzymes that are necessary for conversion of phenazine-1-carboxylic acid (PCA) into pyocyanin (PYO) phenazine in Gram (-) bacterium Pseudomonas aeruginosa. Apparently, the raise in copy number of their genes could increase the amount of pyocyanin phenazine in the microbe. In previous research, two genes phzM and phzS originated from Pseudomonas aeruginosa PS39 strain had been inserted into a Pseudomonas – Escherichia coli shutlle vector pUCP24 to generate a plasmid pUCP24-phzMS. The obtained plasmid had been transformed into P. aeruginosa PS39 strain to create the recombinant P. aeruginosa PS39-phzMS strain. In this study, pUCP24-phzMS was sequenced to verify the polycistronic expression cassette containing both phzM and phzS genes. The results demonstrated that the recombinant plasmid comprised the ori of Pseudomonas and E. coli, gentamicin resistance-cassette, and polycistronic expression cassette for expression of PhzM and PhzS. In which, both genes will be transcripted together in one mRNA strand by the regulation of Lac promoter and operator. The translation from the mRNA to the corresponding proteins will be started by binding ribosome into RBS located upstream of each gene. The nucleotide sequence of these genes were completely homologous (100%) to the submitted sequences MF673740 (phzM) and MF770713 (phzS) on the NCBI GenBank database. Result on assessing the synthesis of pyocyanin in the recombinant strain with the presence of pUCP24-phzMS plasmid showed that pyocyanin concentration in the recombinant strain increased significantly over 2 times (31.22 mg/mL) more than that in the wild strain (13.47 mg/mL). The absorbance at 360 nm of PCA from the P. aeruginosa PS39-phzMS (OD367 = 0.03) strain decreased significantly compared to the one from wild type strain (OD367 = 0.39). Therefore, the plasmid with phzM and phzS genes was proved to improve the pyocyanin biosynthesis through a better conversion of PCA phenazine into PYO via PhzM and PhzS enzymes.
https://link.springer.com/journal/11418/volumes-and-issues/74-4 8/8Online first articles Volumes and issuesNot logged in -210.57.215.182
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