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1.
Natural Product Sciences ; : 261-267, 2015.
Article in English | WPRIM | ID: wpr-7749

ABSTRACT

Compared to their terrestrial and marine counterparts, little is known about the capacity of freshwater-derived actinomycete bacteria to produce novel secondary metabolites. In the current study, we highlight the disparities that exist between cultivation-independent and -dependent analyses of actinomycete communities from four locations in Lake Michigan sediment. Furthermore, through phylogenetic analysis of strains isolated from these locations, we identified a Streptomyces sp., strain B025, as being distinct from other Streptomyces spp. isolated from sediment. Upon fermentation this strain produced a rare class of eight-membered lactone secondary metabolites, which have been for their antitumor properties. We used spectroscopic and chemical derivitization techniques to characterize octalactin B (1) in addition to its corresponding novel, unnatural degradation product (2).


Subject(s)
Bacteria , Fermentation , Fresh Water , Lakes , Michigan , Streptomyces
2.
SPJ-Saudi Pharmaceutical Journal. 2008; 16 (2): 122-134
in English | IMEMR | ID: emr-99311

ABSTRACT

Phytochemical investigation of the aerial parts of Lotus lalambensis Schweinf resulted in the isolation and identification of 20 known compounds. Liquid-Liquid fractionation of the crude extract followed by chromatographic purification resulted in the isolation of lupeol, beta-sitosterol, oleanolic acid, beta-sitosterol glucoside and stigmasterol glucoside from the petroleum ether fraction. The chloroform fraction afforded heptadecanol, kaempferol [1], kaempferol-3-O-alpha-L-rhamnoside [2], lotaustralin [3], epilotaustralin [4], linamarin [5], kaempferol-3,7-di-O-alpha-L-rhamnopyranoside [kaempferitin] [6] and ethyl-O-beta-D-glucopyranoside [7]. From the ethyl acetate fraction three simple rhamnosyl derivatives; butyl-O-alpha-L-rhamnopyranoside [8] methyl-O-alpha-L-rhamnopyranoside [9] and methyl-O-beta-L-rhamnopyranoside [10] were obtained. Kaempferol-3-0-beta-D-glucopy-ranoside-7-O-alpha-L-rhamnopyranoside [11], kaempferol-3-O-alpha- [beta-D-glucopyranosyl-[1""->2'"]- L-rhamnopyranoside]-7-O-alpha-L-rhamnopyranoside [12], kaempferol-3-O-beta-D-glucopyranoside-7-O-alpha-[beta-D-glucopyranosyl-[1""->2'"]-L-rhamnopyranoside] [13] and the myo-inositol [+] D-pinitol [14] were isolated from the butanol extract. The total extract and different fractions were evaluated for their possible estrogenic, anti-inflammatory and anti-platelets aggregation activities. The chloroform extract showed the highest estrogenic activity, while the petroleum ether was the best in protection against inflammation induced by carrageenan. The strongest inhibition of platelet aggregations was observed with the aqueous fraction


Subject(s)
Male , Female , Animals, Laboratory , Plant Extracts , Phytotherapy , Flavonols , Glycosides , Inositol/analogs & derivatives , Rats, Wistar , Anti-Inflammatory Agents , Platelet Aggregation Inhibitors
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