scholarly journals Antifungal Finishing of Fabrics with Natural Dyes from Aerial Biomass of Perilla frutescens (L.) Britton

Author(s):  
Anita Pal ◽  
Rakesh Kumar ◽  
Yogesh Chandra Tripathi

Increased environmental consciousness coupled with detrimental impacts of synthetic dyes and consumers’ concern over hygiene, cleanliness and protection, the demand for functional textiles has increased in recent years. Antimicrobial finishing imparts protective properties to textiles besides attractive shades. The study was aimed to determine the antifungal activity of colourants from aerial biomass of Perilla frutescens and dyed fabrics against pathogenic fungi infesting textiles materials. Antifungal activity of natural dye extracted from aerial biomass of Perilla frutescens against the selected pathogenic fungi viz., Aspergillus niger, Aspergillus flavus, Fusarium moniliforme, Fusarium solani, and Penicillium decumbens was evaluated by agar-well diffusion method. The MIC of the natural dye against each of the test fungi was determined by broth dilution method. Dyed silk, wool and cotton fabrics were also evaluated for antifungal activity by standard method. The natural dye showed antifungal activity against all the five test fungi in a concentration dependent manner. The treatment dose of 1000μg/ml recorded the highest growth reduction in all the test fungi, nearly at par with the positive control. The MICs of natural dye against the test fungi ranged from 32.39 to 36.50μg/ml. All kinds of dyed fabrics also showed remarkable antifungal efficacy against the test fungi. Dyed wool fabric exhibited the maximum growth reduction followed by silk and cotton. The result of the study demonstrated the remarkable antifungal activity of natural dye from Perilla frutescens aerial biomass and dyed fabrics. Therefore, Perilla frutescens can be considered as a potential source of natural dye with functional properties and can be used in protective finishing of different kinds of textile fabrics.

2018 ◽  
Vol 7 (3) ◽  
pp. 230-241
Author(s):  
Savita Joshi ◽  
◽  
Parikshit Kumar ◽  
Prabha Pant ◽  
SC Sati ◽  
...  

Fungicidal activity of 10 ethnobotanically known Kumaun Himalayan gymnospermous plants namely Araucaria cunninghamii, Biota orientalis, Cedrus deodara, Cephalotaxus griffithi, Cryptomeria japonica Cupressus torulosa, Ginkgo biloba, Juniperus communis, Picea smithiana and Pinus wallichiana were tested against six plant disease causing fungal pathogens by agar well-diffusion method. Forty extracts of these gymnospermic leaves in different organic solvents (methanol, ethanol, chloroform and hexane) were studied by performing the 160 sets of experiments. The MIC values of each extract (where % inhibition ≥ 40%) were also determined. All the plant extracts exhibited strong antifungal activity. Results indicated that all leaves extracts of C. griffithi and G. biloba were found most effective among the tested plants extracts. Hexane extract of C. griffithi was showed highest inhibitory activity against C. falcatum (72%; MIC, 7.81µg/ml) and T. indica (70%; MIC, 15.62µg/ml). On the other hand, ethanol extract of G. biloba also showed remarkable activity against P. oryzae (66% with MIC, 7.81g/ml). While P. wallichiana leave extracts were found less active among the studied plants against all the tested fungal strains. The chloroform extracts were found the most effective against all the tested fungi (10% to 60%), followed by ethanol extract (30-50%), methanol extract (20-40%), while in hexane extracts ranged 10-30% only. The extracts of C. griffithi exhibited superior Relative Antifungal Activity (RAA, 20%), followed by G. biloba and A. cunninghamii (RAA, 19 and 12%, respectively). All data were also analyzed for determination of total activity of plant for each studied species of gymnosperm. C. griffithi had maximum activity i.e. 71 % followed by G. biloba (54%) and A. cunninghamii (33%). C. torulosa showed the least total activity and RAA i.e. 8% and 3%, respectively. All the plant species assayed possess definite antifungal properties and suggested for phytochemical analysis to identify the active principles responsible for their antifungal activity


2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Tamirat Bekele Beressa ◽  
Serawit Deyno ◽  
Paul E. Alele

Background. Echinops kebericho is an endemic medicinal plant in Ethiopia widely used in the treatment of infectious and noninfectious diseases. Essential oils are known for their antibacterial, antifungal, antiviral, insecticidal, and antioxidant properties. This study evaluated the antifungal activity of essential oil from E. kebericho against four common pathogenic fungi and two standard strains. Methods. The essential oil was obtained by hydrodistillation. The antifungal screening was done by agar well diffusion method. Minimal inhibitory concentrations (MICs) were determined by broth microdilution. Minimal fungicidal concentrations (MFCs) were determined by subculturing fungal strains with no visible growth onto a Sabouraud dextrose agar (SDA) plate. Results. Candida albicans and Cryptococcus neoformans were highly sensitive while Aspergillus flavus did not show sensitivity up to 1 mg/ml of essential oil; MICs ranged from 0.083 mg/ml to 0.208 mg/ml. Concentration and fungal species showed significant dose-dependent associations ( p < 0.0001 ) with antifungal activity. The MICs of essential oil were comparable to those of the standard drug (fluconazole) against C. glabrata and C. krusei. The lowest MFC of the essential oil was observed against Candida parapsilosis (0.145 mg/ml) while the highest MFC was against Candida krusei (0.667 mg/ml). Conclusion. Echinops kebericho essential oil showed noteworthy antifungal activity against Cryptococcus neoformans, Candida albicans, and Candida glabrata and could be a potential candidate for further antifungal drug development.


1999 ◽  
Vol 43 (12) ◽  
pp. 2950-2959 ◽  
Author(s):  
Elias K. Manavathu ◽  
Jonathan R. Dimmock ◽  
Sarvesh C. Vashishtha ◽  
Pranatharthi H. Chandrasekar

ABSTRACT NC1175 (3-[3-(4-chlorophenyl)-2-propenoyl]-4-[2-(4-chlorophenyl)vinylene]-1-ethyl-4-piperidinol hydrochloride) is a novel thiol-blocking conjugated styryl ketone that exhibits activity against a wide spectrum of pathogenic fungi. Incubation of NC1175 with various concentrations of cysteine and glutathione eliminated its antifungal activity in a concentration-dependent fashion. Since NC1175 is a lipophilic compound that has the potential to interact with cytoplasmic membrane components, we examined its effect on the membrane-located proton-translocating ATPase (H+-ATPase) of yeast (Candida albicans, Candida krusei,Candida guilliermondii, Candida glabrata, andSaccharomyces cerevisiae) and Aspergillus(Aspergillus fumigatus, Aspergillus niger,Aspergillus flavus, and Aspergillus nidulans) species. The glucose-induced acidification of external medium due to H+-ATPase-mediated expulsion of intracellular protons by these fungi was measured in the presence of several concentrations of the drug. NC1175 (12.5 to 50 μM) inhibited acidification of external medium by Candida, Saccharomyces, andAspergillus species in a concentration-dependent manner. Vanadate-inhibited hydrolysis of ATP by membrane fractions of C. albicans was completely inhibited by 50 μM NC1175, suggesting that the target of action of NC1175 in these fungi may include H+-ATPase.


Author(s):  
Rosemary I. Uchegbu ◽  
Jacinta N. Akalazu ◽  
Chinweotuto E. Sokwaibe

Aim: This work was carried out to determine the chemical compositions of Ocimum gratissimum leaf (Fig. 1) using GC-MS and its antifungal potential against some plant pathogenic fungi. Study Design: The study was designed to determine its chemical compositions by GC-MS and to test the inhibitory ability of the plant extract on plant pathogens. Place and Duration of Study: Department of Chemistry, Alvan Ikoku Federal College of Education, Owerri and Department of Plant Science and Biotechnology, Imo State University, Owerri, Nigeria, between February to July 2017. Methodology: The ethanol extract of the leaf of Ocimum gratissimum was evaluated using GC-MS to determine the chemical compositions of the plant. The identification of compounds was done by comparing spectrum of the unknown component with the spectrum of the known components stored in the NIST library. The essential oil of the plant was used to analyze the antifungal potential of the plant. This was done against some plant pathogenic fungi using disc diffusion method and MIC using broth micro dilution method. Results: The GC-MS analysis revealed eight compounds (Fig. 2) with n- Hexadecanoic acid constituting the bulk of the oil (37.21%), followed by Oleic acid (25.38%) and Octadecanoic acid (16.19%). Other compounds present in the plant are Glycyl alcohol (2.47%), Methyl alpha –D- Glucopyranoside (8.33%), Tetradecanoic acid (5.77%), Palmitic amide (2.72%) and d-Glucose, 2,3- diethyl-4,5-dithioacetyl (1.93%). Ocimum gratissimum exhibited different degrees of antifungal activity against the mycelial growth of Aspergillus niger, Botryodiploidia theobromae, Rhizopus stolonifer, Penicillium expansum and Colletotrichum spp and Fusarium oxysporium. The maximum percentage degree inhibition of Ocimum gratissimum oil was observed on A. niger at different concentrations while the least inhibition was observed in Colletotrichum spp at different concentrations. Analysis of some of the compounds found in Ocimum gratissimum such as Methyl alpha.-d-glucopyranoside, Oleic acid etc, reveals the rich pharmacological potential of this medicinal plant and the inhibitory potential of the plant against fungi justify the use of Ocimum gratissimum as a medicine traditionally.


Author(s):  
B. Kpomah ◽  
U. Ugbune ◽  
T. E. Idu

The rapid increase in the number of multidrug-resistant of most pathogenic organisms is fast becoming a global concern, thus, the discovery of novel active pharmacological compounds against new targets is a matter of urgency. The incorporation of metal ions into organic ligands has introduced metal-organic drugs framework with synergistic effects for novel applications in the biological system. In this research work, metal(II) chloride complexes of copper, nickel and zinc containing methylphenylketone thiosemicarbazone (MPK-TSC) with 2,2’-bipyridine (bipy) were synthesized; they were further characterized by satisfactory microelemental analysis, Fourier Transform InfraRed (FTIR) spectra as well as electronic spectra study. The complexes are proposed to have the formulae [L1ML2(Cl2)] where M=metal ion, L1=methylphenylketone thiosemicarbazone   L2=2,2’-bipyridine. The complexes are of 1:2 (metal:ligand) stoichiometry and non-electrolytes in solution, the bidentate nature of the two ligands was evident from the FTIR spectra. The compounds were screened for their antifungal activity against four pathogenic fungi: Aspergillus niger, Penicillium Species, Rizopus and Candida albicans using disc diffusion method. The activities of the complexes have been found to be greater than those of the metal salts and the uncoordinated ligands.


2021 ◽  
Author(s):  
Ahmed Samy ◽  
A. M. Ismail ◽  
Hoda Kabary

Abstract In the present work, Gamma Aluminum oxide (γ-Al2O3) is prepared from wastes (Pepsi Cans). These cans have a structure that contains more than 98 percent aluminum oxide, and they were effectively manufactured to generate nano-sized gamma alumina under mild parameters. Characterization of the prepared nanoparticles are characterizes using different techniques as X-ray diffraction (XRD), High resolution transmission electron microscope (HRTEM), Field Emission Scanning Electron Microscope (FESEM), Attenuated total Reflection-Fourier Transform Infrared (ATR-FTIR), Ultraviolet-Visible (UV-Vis) spectrophotometer and Thermogravimetric analysis (TGA). Also, antifungal activity of γ Al2O3 was applied to widespread pathogenic fungi: Aspergillus flavus, Fusarium oxysporum and Alternaria sp..at different nanoparticles concentrations to determine the maximum fungicidal concentration of the tested nanoparticles on the fungal strains. All characterization confirmed the formation of γ Al2O3 with nearly 2-3 nm and TGA data explains it is thermal stability. By investigating the fungicidal concentration, Data showed the antifungal activity of the selected nanoparticles shows concentration dependent manner based on the fungal strain sensitivity. The maximum antifungal activity of aluminum nanoparticles detected at concentration (3, 6 and 50mg/100ml) with inhibition percentage of (94.2, 95 and 93.3 %) for A flavus, F.oxsporum andAlternaria sp., respectively.


2016 ◽  
Vol 30 (1-2) ◽  
pp. 7-10 ◽  
Author(s):  
Puspa Das ◽  
Shoma Dutta ◽  
Jaripa Begum ◽  
Md Nural Anwar

The essential oil of Pogostemon cablin (Blanco) Benth, also known as Patchouli oil was subjected for its antimicrobial investigation against a panel of ten human pathogenic bacteria and six human pathogenic fungi by Agar well diffusion method and Macrobroth dilution technique using Ampicillin (20ìg/well) and Nystatin (20ìg/well) as control. Antibacterial activity revealed that, the essential oil was more active against Gram positive bacteria than Gram negative bacteria. The largest zone of inhibition was 35 mm (against Bacillus cereus) with 20 ìl of oil. Ditermination of Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) showed that, Bacillus cereus exhibited the lowest MIC (250 ìg/ml) and MBC (750 ìg/ml). The oil showed moderate antifungal activity against all tested organisms. Candida albicans showed greater zone of inhibition (16 mm) than Saccharomyces cerevisiae (14 mm) with 20 ìl and Candida albicans showed lowest MIC and MFC (both were 750 ìg/ml). The zone of inhibition was 25 mm for each filamentous fungal strain with 20 ìl, except for Rhizopus oligosporus (15 mm) and the lowest MIC (250 ìg/ml) and MFC (500 ìg/ml) were reported for Aspergillus fumigatus.Bangladesh J Microbiol, Volume 30, Number 1-2,June-Dec 2013, pp 7-10


Author(s):  
KRISHNAMOORTHI R ◽  
SIVAKUMAR SR

Objective: The objective of this study was to evaluate the antifungal activity of seaweed extracted protein against the pathogenic fungi. Methods: Antifungal activity of seaweed Ulva lactuca L. extracted protein was determined against pathogenic fungi such as Alternaria solani, Aspergillus clavatus, Aspergillus niger, Aspergillus flavus, and Fusarium oxysporum by disk diffusion Method. Then, the potentially active protein was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and circular dichroism (CD) spectroscopy. Results: Seaweeds extracted protein checked for the antifungal activity against A. clavatus, A. solani, and A. flavus better activity compared to standard amphotericin-B and CD spectroscopy. Analysis of the extracts divulges the presence of entire protein compounds. Conclusions: This study extracted seaweed protein sufficient of antifungal activity opposed to antifungal pathogens as compared with the standard. This is first report an activity of seaweed extracted protein against the plant and human pathogenic fungus bearing agricultural important.


2017 ◽  
Vol 3 (4) ◽  
pp. 256 ◽  
Author(s):  
Tirta Kumala Dewi ◽  
Dwi Agustiani ◽  
Sarjiya Antonius

<p class="Els-Abstract-text">Wilt desease of banana caused by <em>Fusarium oxysporum</em> f.sp. <em>cubense</em> (FOC) is one of the most destructive deseases of banana in the tropics. Actinomycetes are the most economically and biotechnologically valuable prokaryotes able to produce wide range of bioactive secondary metabolites. The aims of the present study are to isolate and screen the actinomycetes with high potential ability to produce secondary metabolites that have inhibitory activity against plant pathogenic fungi, <em>Fusarium oxysporum</em> f. sp. <em>cubense</em>. Two isolates from Lampung and Cianjur showed activity against fungi. The isolates designed as L.3.1 and CiIA5b. The metabolites from potent stain was produced by extraction of culture filtrate with ethyl acetate : methanol (4:1), it was tested for their antifungal activity by well diffusion method. Evidence for in vitro antibiosis of L.3.1 and CiIA5b isolates was demonstrated by the zone of fungal-growth inhibition. Production of secondary metabolites was analysis by thin layer chromatography (TLC) and bioautography assays. In this study, the metabolites from L.3.1 and CiIA5b have showed good antifungal activity.</p><div><p class="Els-keywords"><em> </em></p><p class="Els-keywords"><strong>Keywords:</strong> Actinomycetes; antifungal activity; bioautography; secondary metabolites; thin layer chromatography.</p></div>


2019 ◽  
Vol 7 (1) ◽  
pp. 44-54
Author(s):  
Muhaimin Muhaimin ◽  
Syamsurizal Syamsurizal ◽  
Madyawati Latief ◽  
Rahmi Iskandar ◽  
Anis Yohana Chaerunisaa ◽  
...  

Background: Eusiderin A is a neolignan derivate, which makes up the majority of the secondary metabolite of Eusideroxylon zwageri. It has been reported as a potent biopesticide and antifungal agent. Previous studies on the oxidation of terminal methylene of the allylic chain in Eusiderin A have been able to produce primary alcohol, pinacol, and an aldehyde which demonstrated strong activity against plant pathogenic fungi, therefore activity against dermal fungi needs to be studied. Objective: The current study aims to improve the hydrophilicity of Eusiderin A via oxidation of the allylic chain in order to derive a potent antifungal property. Methods: Transformation of Eusiderin A has been achieved by using the Wacker Oxidation Method in combination with the α-Hydroxylation-Ketone Method to produce 7,3’-epoxy-8,4’-oxyneolignane-1’- carboxylic acid. The structure of the 7,3’-epoxy-8,4’-oxyneolignane-1’-carboxylic acid was identified from spectroscopy data. The in vitro antifungal activity study was performed using the paper disc diffusion method against Trichophyton mentagrophytes. Results: New molecule of natural Eusiderin A through the oxidation of the allylic chain to increase the hydrophilicity of Eusiderin A has been designed. Based on the observed UV, IR, 1H and 13C-NMR, and MS spectra, it can be stated that the 7,3’-epoxy-8,4’-oxyneolignane-1’-carboxylic acid has been formed. At a concentration of 50 ppm, this compound showed antifungal activity against Trichophyton mentagrophytes. Conclusion: It can be concluded that the 7,3’-epoxy-8,4’-oxyneolignane-1’-carboxylic acid is a potent antifungal agent as it is able to inhibit the Trichophyton mentagrophytes colonies growth.


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