Abstract. Elfita, Mardiyanto, Fitrya, Larasati JE, Julinar, Widjajanti H, Muharni. 2019. Antibacterial activity of Cordyline fruticosa leaf extracts and its endophytic fungi extracts. Biodiversitas 20: 3804-3812. Endophytic fungi live by forming colonies in plant tissues without harming the host plant. Cordyline fruticose has been used as traditional medicine for the treatment of pathogenic bacterial infections; therefore, its endophytic fungi are expected to have similar activity. In this study, C. fruticosa leaves were extracted with gradient solvents and evaluated for their antibacterial activity using the Kirby–Bauer method against Gram-negative (Salmonella typhi, Escherichia coli) and Gram-positive (Staphylococcus aureus, Bacillus subtilis) bacteria. The extracts of endophytic fungi from C. fruticosa leaves were evaluated for their antibacterial activity, as well. The endophytic fungus with good antibacterial activity was identified by molecular and phylogenetic methods. Chemical compounds from endophytic fungus DB1 were isolated by chromatography and subsequently determined by spectroscopy. The methanol extract of C. fruticosa leaves showed strong antibacterial activity equivalent to the endophytic fungus (DB1). Molecular identification and analysis through the phylogenetic tree showed that the DB1 fungus has a high level of similarity to Neurospora tetrasperma strain APBSDSF108. The antibacterial compounds (compound 1 and 2) isolated from the endophytic fungus DB1 were identified as 4-hydroxy-5-phenylpenta-1,3-dien-1-yl acetate and ergosterol, respectively.
The compound from endophytic fungi of Aspergillus sp. from leaves of kunyit putih (Curcuma zedoaria (Berg.) Roscoe) has been isolated. Isolation begins with cultivation ofAspergillus sp. in 18 L PDB’s media (Potato Dextrose Broth) for 28 days. The liquid cultivation medium was extracted by partitioning method using ethylacetate and then evaporated. The extract was separated and purified by chromatography techniques. Elucidation stucture of the isolated compound was analysis by spectroscopic method NMR 1D and 2D. Antibacterial activity of isolated compound was tested using the disc diffusion method at concentrations 2500, 1000, 500, and 125 ppm. The isolated compounds obtained in the form of a yellow oil (24.30 mg). The 13C NMR spectrum indicated 24 signals of carbon and base on analysis spectrum DEPT 135 showed 5 signal methynes carbon, 1 signals methylene, 9 signals of methyl and 9 signals quarternary carbon. These signals from 1H and 13C-NMR suggested that this compound contained aromatic group and four carbonyl. The isolated compound show antibacterial activity at concentration 2500 ppm which inhibition zone for E. coli, S. dysenteriae, S. aureus, B. subtilis were 10.3 ; 8.3; 8.4; and 7.8 mm, respectively. Based on the analysis result of NMR 1D and 2D, the compound was methyl 6-(5'-(2"-acetoxy-2”-methylpropanoyl)-3"- methyl-2'-(3"'-methylbutanoyl)phenyl)-3-methylbutanoate and has weak antibacterial activity.
Two compounds from cultivation of the endophytic fungi Penicillium sp of leaves of kunyit putih (Curcuma zedoaria have been isolated. The endophytic fungus was cultivated on 5 L of Potatos Dextrose Broth (PDB) medium at room temperature (no shaking) for 3 weeks. The cultures were extracted with ethyl acetate to afford 3.0 g of residue after removal of the solvent under reduced pressure. The extract was separated and purified by silica gel column chromatography (CC) and afforded two pure compounds as colorless oily liquid (compound 1) and yellow crystal (compound 2). The structure of these compounds were characterized by detailed UV, IR, and NMR spectroscopic analysis and compound 1 as well as comparison with the reported data. Base on spectra analysis the compound 1 was determined as Di-(2-ethylhexyl)phthalate and compound 2 as 5-(4’-ethoxy-2’-hydroxy-5’-methyl-2’,3’-dihydrofuran-3’-il (hydroxy) methyl-4-isopropyl-3-methyl-2-pyran-2-on). Compound 1 is not new compound, but it is new for endophytic fungus from C. zeodoria and compound 2 is new compound.
A flavonoid compound was isolated from dried rihzomes of tunjuk langit (Helminthostachis zaylanica Lin), a traditional medicine from South Sumatera, Indonesia. Extraction was done by maceration methode and separation of isolated compound was conducted by chromatographic technique. The structure of this compound was determined base on spectroscopic data such as including UV, IR, 1-D, 2-D NMR, and comparison with the reported data. Based on spectral data analysis, concluded that isolated compound was Ugonin J (5,7,3',4'-tetrahydroxy-6-(6,6-dimethyil-2-methylenecyclo-hexylmethyl)flavone). Keywords: Flavonoid, Ugonin J, Helmintohostacys zaylanica
Parkia speciosa (petai) pods are rarely used and considered as waste despite their phenolic and flavonoid content. Phenolic and flavonoid content in plants are known to exhibit antioxidant activity. Antioxidants are known to potentially act agains radical and mediate the damage by structural stabilization. This research was conducted to analyze the antioxidant potential of petai pods using DPPH method. Analysis showed the IC50 of petai pods ethanolic extract was 75.72 ppm, which indicate strong acting antioxidant. Standardization of extracts were determined to manage the quality of extract, including the analysis of density, water content, ash values, and quantification of total phenolic and flavonoid content. Research outcome indicate the extract retain its quality during storage and use which confrmed to standardization requirements of water content and ash values. Total phenolics and flavonoid obtained were 272.45 mg/gGAE and 243.2029 mg/gQE respectively. Based from this research, petai pods ethanolic extract present strong antioxidant activity which was contributed by high existing content of flavonoid and phenolic compounds.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.