Analysis of the effectiveness of Tulbaghia Violacea extracts as devulcanizing agents for synthetic CIS-1,4-polyisoprene vulcanizates
- Authors: Gxakuma, Lutho
- Date: 2020
- Subjects: Plant extracts , Plant products -- South Africa Medicinal plants -- South Africa Plants -- Analysis
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10948/49093 , vital:41600
- Description: Tulbaghia violacea is an indigenous plant commonly known as wild garlic, wilde knoffel in Afrikaans, isihaqa in Zulu or itswele lomlambo in Xhosa. Its leaves and bulbs are widely used as herbal remedies for various ailments and its medicinal uses include fever and colds, asthma, tuberculosis and stomach problems. Like all other members of the Alliacea family, Tulbaghia violacea produces a distinctive garlic-like odour when its leaves or rhizomes are damaged, resulting in the release of cysteine-derived sulphur compounds which include the oil-soluble organo-sulphur compounds and water-soluble cysteine derivatives. Chemically synthesized sulphur containing compounds have been reported to be effective devulcanizing agents and many industries prefer to perform devulcanization using them. Most commonly applied devulcanizing agents include disulphides, thiophenols and their zinc salts, and mercaptans which are mixed with the rubber scrap powder under specific reaction conditions. In this study, instead of performing devulcanization by using industrial synthesized sulphur containing compounds, the effectiveness of the extracts of organo-sulphur containing compounds from Tulbaghia violacea are evaluated as potential devulcanizing agents for synthetic cis-1,4-polyisoprene vulcanizates. This is a new, cheap and greener practice of rubber devulcanization. Diallyl disulphide, which is one of the organo-sulphur containing compounds present in Tulbaghia violacea, is the devulcanizing agent of interest to this study. The organo-sulphur containing compounds were extracted from the bulbs, roots and leaves of the plant using the soxhlet and ultrasonic bath extraction method. The solvent system used in the soxhlet extraction method was 2% of 2-propanol in n-hexane whereas in ultrasonic bath extraction method the solvent system used was 100% ethanol. An essential oil extract was obtained from the plant organs. The yield of the essential oil extracts obtained using the soxhlet extraction method was higher compared to the yield of the essential oil extracts obtained using the ultrasonic bath extraction method. According to the Fourier-Transform Infrared spectroscopy, the organo-sulphur containing compounds were present in the essential oil extracts of the plant. The essential oil extracts that were extracted using the soxhlet extraction method were chosen for further analysis. It was found out that the allyl sulphide and diallyl disulphide have the same retention time from the High Performance Liquid Chromatography (using a normal phase column). The Differential Scanning Calorimeter indicated that the allyl sulphide was not present in the essential oil extracts whereas the diallyl disulphide was present in the essential oil extract of the roots and leaves. The High Performance Liquid Chromatography was used to quantify the presence of the diallyl disulphide in the essential oil extract of roots and leaves. The quantity of diallyl disulphide was 23% in the dry mass of the essential oil extract of roots. In the essential oil extract of leaves the diallyl disulphide was very low concentrated and the High Performance Liquid Chromatography was less sensitive to detect it. According to the Thermogravimetric Analyser, it was found that the essential oil extracts begin to degrade at 120 °C and experience a multistage degradation. The softening temperature of the essential oil extracts was 60 °C from the Simultaneous Differential Scanning Calorimeter-Thermogravimetric Analyser. Conventional vulcanization of synthetic cis-1,4-polyisoprene was prepared with the vulcanization ingredients of zinc oxide, sulphur, stearic acid and N-tert-butyl-2-benzothiazole sulphenamide. The vulcanized synthetic cis-1,4-polyisoprene produced, under the heating temperature of 160 °C, was mixed with the essential oil extracts using the internal mixer at 60 °C and the two-roll mill. The overall torque, tan delta and the total crosslink density were the properties of interest of synthetic cis-1,4-polyisoprene vulcanizate in this study. The devulcanization temperature for the treated synthetic cis-1,4-polyisoprene vulcanizate with the essential oil extracts was optimized using the Dynamic Moving Die Rheometer and Dynamic Rubber Process Analyser. The amount of essential oil extracts at which they are effective devulcanizing agents for synthetic cis-1,4-polyisoprene vulcanizate was also optimized. During optimization a change on the latter mentioned properties of synthetic cis-1,4-polyisoprene vulcanizate was observed, indicating that the essential oil extracts have an effect as potential devulcanizing agents. The essential oil extracts increased the tan delta and reduced the overall torque, and total crosslink density of synthetic cis-1,4-polyisoprene vulcanizate as expected from devulcanizing agents. 200 °C was a preferable devulcanization temperature whereas essential oil extracts were effective as devulcanizing agent at 1.4%. However, the essential oil extracts influenced the overall torque and tan delta of synthetic cis-1,4-polyisoprene vulcanizate during the mixing process in the internal mixer at 60 °C, which was before heating at 200 °C. The essential oil extracts had a higher influence on the overall torque of synthetic cis-1,4-polyisoprene vulcanizate under heating at 200 °C whereas at 60 °C, during the mixing process, they had a higher influence on the tan delta of synthetic cis-1,4-polyisoprene vulcanizate. The essential oil extract of leaves had a higher influence on the overall torque whereas the essential oil extract of bulbs had a higher influence on the tan delta of synthetic cis-1,4-polyisoprene vulcanizate at 200 °C. The essential oil extract of roots shown a greater influence on the overall torque and tan delta of synthetic cis-1,4-polyisoprene vulcanizate at 60 °C during the mixing process. The effect of the essential oil extracts on the reversing heat capacity of synthetic cis-1,4-polyisoprene vulcanizate was also investigated using the Modulated Differential Scanning Calorimetry method. The essential oil extract of bulbs and roots influenced the reversing heat capacity of synthetic cis-1,4-polyisoprene vulcanizate by reducing it whereas the essential oil extract of leaves caused a temperature shift of the reversing heat capacity curve from the Modulated Differential Scanning Calorimeter thermogram of synthetic cis-1,4-polyisoprene vulcanizate. Therefore, the results indicated that the essential oil extracts of Tulbaghia violacea have an effect as an alternative potential devulcanizing agents for conventional vulcanized synthetic cis-1,4-polyisoprene whether the diallyl disulphide compound is present or not in them.
- Full Text:
- Date Issued: 2020
- Authors: Gxakuma, Lutho
- Date: 2020
- Subjects: Plant extracts , Plant products -- South Africa Medicinal plants -- South Africa Plants -- Analysis
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10948/49093 , vital:41600
- Description: Tulbaghia violacea is an indigenous plant commonly known as wild garlic, wilde knoffel in Afrikaans, isihaqa in Zulu or itswele lomlambo in Xhosa. Its leaves and bulbs are widely used as herbal remedies for various ailments and its medicinal uses include fever and colds, asthma, tuberculosis and stomach problems. Like all other members of the Alliacea family, Tulbaghia violacea produces a distinctive garlic-like odour when its leaves or rhizomes are damaged, resulting in the release of cysteine-derived sulphur compounds which include the oil-soluble organo-sulphur compounds and water-soluble cysteine derivatives. Chemically synthesized sulphur containing compounds have been reported to be effective devulcanizing agents and many industries prefer to perform devulcanization using them. Most commonly applied devulcanizing agents include disulphides, thiophenols and their zinc salts, and mercaptans which are mixed with the rubber scrap powder under specific reaction conditions. In this study, instead of performing devulcanization by using industrial synthesized sulphur containing compounds, the effectiveness of the extracts of organo-sulphur containing compounds from Tulbaghia violacea are evaluated as potential devulcanizing agents for synthetic cis-1,4-polyisoprene vulcanizates. This is a new, cheap and greener practice of rubber devulcanization. Diallyl disulphide, which is one of the organo-sulphur containing compounds present in Tulbaghia violacea, is the devulcanizing agent of interest to this study. The organo-sulphur containing compounds were extracted from the bulbs, roots and leaves of the plant using the soxhlet and ultrasonic bath extraction method. The solvent system used in the soxhlet extraction method was 2% of 2-propanol in n-hexane whereas in ultrasonic bath extraction method the solvent system used was 100% ethanol. An essential oil extract was obtained from the plant organs. The yield of the essential oil extracts obtained using the soxhlet extraction method was higher compared to the yield of the essential oil extracts obtained using the ultrasonic bath extraction method. According to the Fourier-Transform Infrared spectroscopy, the organo-sulphur containing compounds were present in the essential oil extracts of the plant. The essential oil extracts that were extracted using the soxhlet extraction method were chosen for further analysis. It was found out that the allyl sulphide and diallyl disulphide have the same retention time from the High Performance Liquid Chromatography (using a normal phase column). The Differential Scanning Calorimeter indicated that the allyl sulphide was not present in the essential oil extracts whereas the diallyl disulphide was present in the essential oil extract of the roots and leaves. The High Performance Liquid Chromatography was used to quantify the presence of the diallyl disulphide in the essential oil extract of roots and leaves. The quantity of diallyl disulphide was 23% in the dry mass of the essential oil extract of roots. In the essential oil extract of leaves the diallyl disulphide was very low concentrated and the High Performance Liquid Chromatography was less sensitive to detect it. According to the Thermogravimetric Analyser, it was found that the essential oil extracts begin to degrade at 120 °C and experience a multistage degradation. The softening temperature of the essential oil extracts was 60 °C from the Simultaneous Differential Scanning Calorimeter-Thermogravimetric Analyser. Conventional vulcanization of synthetic cis-1,4-polyisoprene was prepared with the vulcanization ingredients of zinc oxide, sulphur, stearic acid and N-tert-butyl-2-benzothiazole sulphenamide. The vulcanized synthetic cis-1,4-polyisoprene produced, under the heating temperature of 160 °C, was mixed with the essential oil extracts using the internal mixer at 60 °C and the two-roll mill. The overall torque, tan delta and the total crosslink density were the properties of interest of synthetic cis-1,4-polyisoprene vulcanizate in this study. The devulcanization temperature for the treated synthetic cis-1,4-polyisoprene vulcanizate with the essential oil extracts was optimized using the Dynamic Moving Die Rheometer and Dynamic Rubber Process Analyser. The amount of essential oil extracts at which they are effective devulcanizing agents for synthetic cis-1,4-polyisoprene vulcanizate was also optimized. During optimization a change on the latter mentioned properties of synthetic cis-1,4-polyisoprene vulcanizate was observed, indicating that the essential oil extracts have an effect as potential devulcanizing agents. The essential oil extracts increased the tan delta and reduced the overall torque, and total crosslink density of synthetic cis-1,4-polyisoprene vulcanizate as expected from devulcanizing agents. 200 °C was a preferable devulcanization temperature whereas essential oil extracts were effective as devulcanizing agent at 1.4%. However, the essential oil extracts influenced the overall torque and tan delta of synthetic cis-1,4-polyisoprene vulcanizate during the mixing process in the internal mixer at 60 °C, which was before heating at 200 °C. The essential oil extracts had a higher influence on the overall torque of synthetic cis-1,4-polyisoprene vulcanizate under heating at 200 °C whereas at 60 °C, during the mixing process, they had a higher influence on the tan delta of synthetic cis-1,4-polyisoprene vulcanizate. The essential oil extract of leaves had a higher influence on the overall torque whereas the essential oil extract of bulbs had a higher influence on the tan delta of synthetic cis-1,4-polyisoprene vulcanizate at 200 °C. The essential oil extract of roots shown a greater influence on the overall torque and tan delta of synthetic cis-1,4-polyisoprene vulcanizate at 60 °C during the mixing process. The effect of the essential oil extracts on the reversing heat capacity of synthetic cis-1,4-polyisoprene vulcanizate was also investigated using the Modulated Differential Scanning Calorimetry method. The essential oil extract of bulbs and roots influenced the reversing heat capacity of synthetic cis-1,4-polyisoprene vulcanizate by reducing it whereas the essential oil extract of leaves caused a temperature shift of the reversing heat capacity curve from the Modulated Differential Scanning Calorimeter thermogram of synthetic cis-1,4-polyisoprene vulcanizate. Therefore, the results indicated that the essential oil extracts of Tulbaghia violacea have an effect as an alternative potential devulcanizing agents for conventional vulcanized synthetic cis-1,4-polyisoprene whether the diallyl disulphide compound is present or not in them.
- Full Text:
- Date Issued: 2020
In vitro cytotoxic effects of selected Nigerian medicinal plant extracts on cancer cell lines
- Authors: Baatjies, Lucinda
- Date: 2012
- Subjects: Cancer -- Treatment , Cancer cells , Medicinal plants , Plant extracts , Traditional medicine , Public health
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:10316 , http://hdl.handle.net/10948/d1008191 , Cancer -- Treatment , Cancer cells , Medicinal plants , Plant extracts , Traditional medicine , Public health
- Description: Cancer is a disease that imposes a heavy burden on public health and poses a challenge to science. The World Health Organization estimates that 80 percent of people in developing countries of the world rely on traditional medicine for their primary health needs, and about 85 percent of traditional medicine involves the use of plant extracts. This is particularly true in Africa where a large percentage of the population depends upon medicinal plants for health care. Therefore, detailed screening and evaluation of bioactive substances for chemotherapeutic purposes of African plants are urgently warranted. Furthermore, this will serve to validate the efficacy and safety of African traditional medicine. The current study investigated the in vitro cytotoxic effects of 17 ethanolic extracts of the following 16 plants used in traditional anticancer medicine in Nigeria: Sapium ellipticum leaves, Sapium ellipticum stembark, Combretum paniculatum, Celosia trigyna, Pupalia lappacea, Justica extensa, Hedranthera barteri leaves, Alternanthera sessilis, Ethulia conyzoides leaves, Lannea nigritana stembark, Combretum zenkeri root, Combretum molle leaves, Adenanthera parvoniana, Lannea acida, Cyathula achyranthoides, Drymaria cordata, Cyathula prostrata, against HeLa cancer cells. Five of the most promising extracts (Sapium ellipticum leaves, Combretum paniculatum, Celosia trigyna, Drymaria cordata, Cyathula prostrata) were selected for further screening against HT29 and MCF-7 cancer cells. Of the five, the first two were investigated further based on their activities in the screening phase. The S. ellipticum leaf extract yielded IC50 values of 88.60 ± 0.03 and 93.03 ± 0.03 μg/ml against HeLa and MCF-7, respectively. The toxicity was also evaluated on normal cells and an IC50 of 77.66 μg/ml was obtained for peripheral blood mononuclear cells (PBMCs). The IC50 values for proliferating and confluent Chang liver cells were both >125 μg/ml. These results suggest that the extract may be selective for specific cell types. Bio-assay guided fractionation of the S. ellipticum ethanolic extract yielded two active fractions; chloroform and ethyl acetate. Two compounds isolated from the chloroform extract were screened against the three cancer cell lines and found to be inactive. Three compounds were isolated from the ethyl acetate fraction and revealed IC50 values < 62.5 and < 31 μg/ml against MCF-7. Unfortunately these two compounds soon lost activity before any further work could be done on them and work was continued with the crude extract.
- Full Text:
- Date Issued: 2012
- Authors: Baatjies, Lucinda
- Date: 2012
- Subjects: Cancer -- Treatment , Cancer cells , Medicinal plants , Plant extracts , Traditional medicine , Public health
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:10316 , http://hdl.handle.net/10948/d1008191 , Cancer -- Treatment , Cancer cells , Medicinal plants , Plant extracts , Traditional medicine , Public health
- Description: Cancer is a disease that imposes a heavy burden on public health and poses a challenge to science. The World Health Organization estimates that 80 percent of people in developing countries of the world rely on traditional medicine for their primary health needs, and about 85 percent of traditional medicine involves the use of plant extracts. This is particularly true in Africa where a large percentage of the population depends upon medicinal plants for health care. Therefore, detailed screening and evaluation of bioactive substances for chemotherapeutic purposes of African plants are urgently warranted. Furthermore, this will serve to validate the efficacy and safety of African traditional medicine. The current study investigated the in vitro cytotoxic effects of 17 ethanolic extracts of the following 16 plants used in traditional anticancer medicine in Nigeria: Sapium ellipticum leaves, Sapium ellipticum stembark, Combretum paniculatum, Celosia trigyna, Pupalia lappacea, Justica extensa, Hedranthera barteri leaves, Alternanthera sessilis, Ethulia conyzoides leaves, Lannea nigritana stembark, Combretum zenkeri root, Combretum molle leaves, Adenanthera parvoniana, Lannea acida, Cyathula achyranthoides, Drymaria cordata, Cyathula prostrata, against HeLa cancer cells. Five of the most promising extracts (Sapium ellipticum leaves, Combretum paniculatum, Celosia trigyna, Drymaria cordata, Cyathula prostrata) were selected for further screening against HT29 and MCF-7 cancer cells. Of the five, the first two were investigated further based on their activities in the screening phase. The S. ellipticum leaf extract yielded IC50 values of 88.60 ± 0.03 and 93.03 ± 0.03 μg/ml against HeLa and MCF-7, respectively. The toxicity was also evaluated on normal cells and an IC50 of 77.66 μg/ml was obtained for peripheral blood mononuclear cells (PBMCs). The IC50 values for proliferating and confluent Chang liver cells were both >125 μg/ml. These results suggest that the extract may be selective for specific cell types. Bio-assay guided fractionation of the S. ellipticum ethanolic extract yielded two active fractions; chloroform and ethyl acetate. Two compounds isolated from the chloroform extract were screened against the three cancer cell lines and found to be inactive. Three compounds were isolated from the ethyl acetate fraction and revealed IC50 values < 62.5 and < 31 μg/ml against MCF-7. Unfortunately these two compounds soon lost activity before any further work could be done on them and work was continued with the crude extract.
- Full Text:
- Date Issued: 2012
Evaluation of plant extracts : artemisia afra and annona muricata for inhibitory activities against mycobacterium tuberculosis and human immunodeficiency virus
- Authors: Pruissen, Megan Colleen
- Date: 2013
- Subjects: Plant extracts , Medicinal plants -- South Africa , Tuberculosis -- Alternative treatment -- South Africa
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:10341 , http://hdl.handle.net/10948/d1019845
- Description: Mycobacterium tuberculosis and Human Immuno-Deficiency Virus (HIV) have a high prevalence in South Africa. The development and spread of drug resistant tuberculosis is a serious problem which is exacerbated by tuberculosis (TB) co-infection in HIV patients. Traditional medicinal plants like Annona muricata and Artemisia afra are used for respiratory ailments and antiviral therapies respectively. The aim of this study was to evaluate Annona muricata (ethanolic extract) and Artemisia afra (ethanolic and aqueous extracts) for inhibitory activities against M. tuberculosis and HIV. In vitro bioassays for anti-TB activity included: microplate alamar blue assay (MABA), flow cytometry and ρ-iodonitrotetrazolium chloride assays while anti-HIV activity was determined using an HIV-1 reverse transcriptase colorimetric ELISA kit and an HIV-1 integrase colorimetric immunoassay. Cytotoxicity of plant extracts were assessed by the MTT assay on Chang Liver and HepG2 cells. Potential synergistic effects were determined using the basis of Combination Index. Potential interactions of plant extracts with drug metabolic pathways were evaluated with the Glutathione-S-Transferase assay kit as well as the CYP3A4 assay kit. A. muricata ethanolic extract exhibited anti-TB activity with MIC 125 μg/mL. MABA was shown to be the most sensitive and effective method for the detection of anti-TB activity. Artemisia afra aqueous extract showed HIV-1 reverse transcriptase inhibition exhibiting ˃85 percent inhibition at 1 mg/mL while the ethanolic extracts of A. afra and A. muricata showed inhibition of HIV-1 integrase activity at ˃86.8 percent and ˃88.54 percent respectively at concentrations >0.5 - 4 mg/mL. The aqueous extract of A. afra displayed inhibition of HIV-1 integrase ˃52.16 percent at 0.5 mg/mL increasing to 72.89 percent at 4 mg/ml of the extract. A. muricata was cytotoxic at an IC50 of 30 μg/mL and 77 μg/mL on Chang Liver and HepG2 cells respectively, whilst A. afra aqueous and ethanol extracts were not cytotoxic to both cell lines. The ethanolic extract of A. muricata showed both antagonistic and synergistic properties at various IC values, when used in conjunction with rifampicin. A. afra ethanolic extract interrupted GST activity while aqueous extracts of A. afra and A. muricata had a slight effect. All extracts interrupted CYP3A4 activity, however the ethanolic extracts of A. muricata and A. afra showed greater inhibition than the aqueous extract of A. afra. These extracts should be investigated further as they could be an important source of compounds for treatment of M. tuberculosis and HIV respectively.
- Full Text:
- Date Issued: 2013
- Authors: Pruissen, Megan Colleen
- Date: 2013
- Subjects: Plant extracts , Medicinal plants -- South Africa , Tuberculosis -- Alternative treatment -- South Africa
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:10341 , http://hdl.handle.net/10948/d1019845
- Description: Mycobacterium tuberculosis and Human Immuno-Deficiency Virus (HIV) have a high prevalence in South Africa. The development and spread of drug resistant tuberculosis is a serious problem which is exacerbated by tuberculosis (TB) co-infection in HIV patients. Traditional medicinal plants like Annona muricata and Artemisia afra are used for respiratory ailments and antiviral therapies respectively. The aim of this study was to evaluate Annona muricata (ethanolic extract) and Artemisia afra (ethanolic and aqueous extracts) for inhibitory activities against M. tuberculosis and HIV. In vitro bioassays for anti-TB activity included: microplate alamar blue assay (MABA), flow cytometry and ρ-iodonitrotetrazolium chloride assays while anti-HIV activity was determined using an HIV-1 reverse transcriptase colorimetric ELISA kit and an HIV-1 integrase colorimetric immunoassay. Cytotoxicity of plant extracts were assessed by the MTT assay on Chang Liver and HepG2 cells. Potential synergistic effects were determined using the basis of Combination Index. Potential interactions of plant extracts with drug metabolic pathways were evaluated with the Glutathione-S-Transferase assay kit as well as the CYP3A4 assay kit. A. muricata ethanolic extract exhibited anti-TB activity with MIC 125 μg/mL. MABA was shown to be the most sensitive and effective method for the detection of anti-TB activity. Artemisia afra aqueous extract showed HIV-1 reverse transcriptase inhibition exhibiting ˃85 percent inhibition at 1 mg/mL while the ethanolic extracts of A. afra and A. muricata showed inhibition of HIV-1 integrase activity at ˃86.8 percent and ˃88.54 percent respectively at concentrations >0.5 - 4 mg/mL. The aqueous extract of A. afra displayed inhibition of HIV-1 integrase ˃52.16 percent at 0.5 mg/mL increasing to 72.89 percent at 4 mg/ml of the extract. A. muricata was cytotoxic at an IC50 of 30 μg/mL and 77 μg/mL on Chang Liver and HepG2 cells respectively, whilst A. afra aqueous and ethanol extracts were not cytotoxic to both cell lines. The ethanolic extract of A. muricata showed both antagonistic and synergistic properties at various IC values, when used in conjunction with rifampicin. A. afra ethanolic extract interrupted GST activity while aqueous extracts of A. afra and A. muricata had a slight effect. All extracts interrupted CYP3A4 activity, however the ethanolic extracts of A. muricata and A. afra showed greater inhibition than the aqueous extract of A. afra. These extracts should be investigated further as they could be an important source of compounds for treatment of M. tuberculosis and HIV respectively.
- Full Text:
- Date Issued: 2013
The effect of tulbaghia violacea plant extract on the growth of aspergillus species
- Authors: Belewa, Xoliswa Vuyokazi
- Date: 2009
- Subjects: Plant products , Plant extracts , Traditional medicine
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:10315 , http://hdl.handle.net/10948/d1008186 , Plant products , Plant extracts , Traditional medicine
- Description: Traditional medicine has become an important part of healthcare worldwide. It is estimated that about 25 percent of prescribed medicines contain plant products or active compounds derived from plants. In South Africa, traditional medicine forms part of the culture and tradition of most communities. Garlic compounds have been shown to have a variety of antimicrobial properties. Amongst these are antifungal, antibacterial, antiviral and anti protozoal activities. Allicin and its breakdown products have been shown to be the main active compounds which possess these properties. Tulbaghia violacea has been used for the treatment of a variety of illnesses including asthma, fever, oesophageal cancer, constipation and hypertension. This study investigated the antifungal nature of T.violacea on the morphology, spore germination and lipid synthesis of Aspergillus flavus and Aspergillus parasiticus. The results of this study showed that the plant extract inhibited A. flavus growth at a minimal inhibitory concentration of 15mg/ml and was fungicidal at 20mg/ml and above. A. parasiticus was not inhibited at 25mg/ml indicating resistance to the inhibitory component of the plant extract. A measure of metabolic activity using the XTT assay showed reduced metabolic activity in the presence of increasing concentrations of the plant extract. Higher extract concentrations resulted in higher percentage inhibition of fungal growth for both fungal species with up to 98 percent inhibition being observed for the highest extract concentrations for both fungi. Germination was also delayed in the presence of 15mg/ml plant extract concentration by up to 60hr for A. flavus and 48hr for A. parasititcus. The TEM results showed increased thickening of the cell wall with higher extract concentrations. The thickening was greater for A. flavus than for A. parasiticus. Cell wall thickening may be the reason for the delay in germination in both species. Lipid production was reduced in the presence of plant extracts when compared to the control. The plant extracts inhibited triglyceride production at 15mg/ml for both A. flavus and A. parasiticus. The results therefore indicate that T. violacea extracts are antifungal and probably affect germination through interactions with the cell wall. It is possible that the extract affects lipid production in Aspergillus species.
- Full Text:
- Date Issued: 2009
- Authors: Belewa, Xoliswa Vuyokazi
- Date: 2009
- Subjects: Plant products , Plant extracts , Traditional medicine
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:10315 , http://hdl.handle.net/10948/d1008186 , Plant products , Plant extracts , Traditional medicine
- Description: Traditional medicine has become an important part of healthcare worldwide. It is estimated that about 25 percent of prescribed medicines contain plant products or active compounds derived from plants. In South Africa, traditional medicine forms part of the culture and tradition of most communities. Garlic compounds have been shown to have a variety of antimicrobial properties. Amongst these are antifungal, antibacterial, antiviral and anti protozoal activities. Allicin and its breakdown products have been shown to be the main active compounds which possess these properties. Tulbaghia violacea has been used for the treatment of a variety of illnesses including asthma, fever, oesophageal cancer, constipation and hypertension. This study investigated the antifungal nature of T.violacea on the morphology, spore germination and lipid synthesis of Aspergillus flavus and Aspergillus parasiticus. The results of this study showed that the plant extract inhibited A. flavus growth at a minimal inhibitory concentration of 15mg/ml and was fungicidal at 20mg/ml and above. A. parasiticus was not inhibited at 25mg/ml indicating resistance to the inhibitory component of the plant extract. A measure of metabolic activity using the XTT assay showed reduced metabolic activity in the presence of increasing concentrations of the plant extract. Higher extract concentrations resulted in higher percentage inhibition of fungal growth for both fungal species with up to 98 percent inhibition being observed for the highest extract concentrations for both fungi. Germination was also delayed in the presence of 15mg/ml plant extract concentration by up to 60hr for A. flavus and 48hr for A. parasititcus. The TEM results showed increased thickening of the cell wall with higher extract concentrations. The thickening was greater for A. flavus than for A. parasiticus. Cell wall thickening may be the reason for the delay in germination in both species. Lipid production was reduced in the presence of plant extracts when compared to the control. The plant extracts inhibited triglyceride production at 15mg/ml for both A. flavus and A. parasiticus. The results therefore indicate that T. violacea extracts are antifungal and probably affect germination through interactions with the cell wall. It is possible that the extract affects lipid production in Aspergillus species.
- Full Text:
- Date Issued: 2009
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