This study examines field cropping constraints for domestication of an endangered, wild medicinal plant, Siphonochilus aethiopicus, (Schweif.) B.L. Burt. Extensive literature review and careful observations of plant growth behavior during two years of crop trials overturned several long-held but erroneous claims that have consistently appeared in the scholarly literature, and revealed previously undocumented plant growth characteristics. S. aethiopicus (Schweif.) B.L. Burt. is a rhizomatous corm, not a rhizome. Field growth observations demonstrated clearly that the false stem and leaves grow continuously from emergence in September to senescence in April-May; the corm retains its tuberous roots during winter senescence, and is genetically preprogrammed to shoot in September. Flowers may emerge throughout the growing season (not only initially prior to shoot emergence), typical leaf count is 11-15, not 6-8 as previously reported, numbers that remain constant even when the plant height increases by 20-30% under shade, and leaf distichy is independent of the sun’s course and is unaffected by mother corm orientation. S. aethiopicus proved to be unusually resistant to common field diseases and pests, and resilient to severe hail. The responses of S. aethiopicus were tested in a series of field trials to the effects of levels of compost, field spacing, size of planting material, addition of biocontrol agents, different degrees of shading, and factorials of the macronutrients Nitrogen, Phosphorous and Potassium. Spacing-Composted chicken litter combinations were tested in 2005-2006 in factorial combination with Spacing at 15 cm-4.5 kg ha-1, 20 cm-7.5 kg ha-1, 30 cm-10 kg ha-1, and 40 cm-15.5 kg ha-1, and these treatments were randomized with 4 Corm planting sizes (height by base diameter in mm): Small (S, 12.38 mm x 12.6 mm), Medium Small (MS, 29.65 mm x 27.93 mm), Medium Large (ML, 38.48 mm x 37.78 mm) and Large (L, 52.37 mm x 44.10 mm). 2005-2006 ANOVA tests showed significant differences between Spacing-Compost and Corm Size for the total harvest biomass measure, with 30 cm and 40 cm spaces better than 15 cm spacing, and Corm Size MS, ML and L all better than S, and ML better than MS. Total Corms harvested per block and ii Survival Percentage were similarly significant for Corm Size, but not Spacing. Corms smaller than the Small criteria were raised separately, under optimal conditions in a nursery. In a separate 2005-2006 Compost-only trial ANOVA tests did not find significant differences between compost levels. In 2006-2007 we tested Spacing separately at 5, 10, 15, 20, 30 and 40 cm between planted corms in each plot. We tested Compost levels separately, with 0, 5, 10 and 15 kg ha-1 compost per plot. In 2006-2007 only the ML and L sizes were used in an even mix. There were no significant differences between treatments due to high experimental error, but measurement across all production parameters showed a clear trend towards best performance at spacing between 20 and 40 cm. Overall the results from the Spacing, Compost-level and Corm Size trials suggest that 30 cm is perhaps the optimal field spacing, higher compost levels tend to give better results, and the ML and L corm sizes perform better in open-sun field trials. These parameters are recommended for further field studies and production. The effects of two commercial strains of Trichoderma spp were tested at recommended doses applied to S. aethiopicus. T. harzianum Strain B77 was used as a drench at planting in comparison with a Control and a fungicide in 2005-2006. There were no significant differences between treatments for Harvested Biomass or Survival Percentage. B77 did perform significantly better than the Fungicide in the Total Corm measurement, but neither treatment was significantly different from the Control. In sum, there was a weak trend towards a greater number of output corms as a result of the application of the biocontrol agent. In both 2005-2006 and 2006-2007 we tested T. harzianum Strain kd applied as a drench at planting, with a second drench at 4 weeks. In 2006-2007 there were no significant differences between treatments, but the trend was towards better performance as a result of the drench at planting only. In 2005-2006 open field trials had shown that S. aethiopicus is susceptible to sunburn and Erwinia soft rot when grown in the full sun. Therefore, we tested the effect of various shadecloth densities and colours on production performance in 2006-2007. Treatments were Control (full sun), 40% White (TiO2) (23% shade), 40% Grey (28-30% shade), Light Black (40%), Medium Black (50%), Dark Black (80%), and Red (40%). There were no significant differences between treatments, but the trends indicated that the Control (full sun) and Dark Black (80% shade) performed the worst. Colour of shade did not appear to be important, and plants under all the shadecloths with 40-50% shade grew best. In a factorial trial different levels of Nitrogen, Phosphorous, and Potassium (NPK)were tested, over two seasons. Four levels of each input were used: N at 0 (Control), 40 kg ha-1 (N1), 80 kg ha-1 (N1), and 120 kg ha-1 (N3). P levels were 0 (Control) 60 kg ha-1 (P1) ,120 kg ha-1 (P2) and 200 kg ha-1 (P3). K levels were 0 (Control), 100 kg ha-1 (K1), 200 kg ha-1 (K2), and 400 kg ha-1 (K3). In 2005-2006 there were no significant differences between treatments. In 2006-2007 data there were significant results for Nitrogen only within each repetition. However, significance disappeared when combining across repetitions. We then ran a Bootstrap re-sampling analysis of both 2005-2006 and 2006-2007 data (data were analyzed separately because of different plot sizes and corm numbers in the two years), looking at the optimal level of each macronutrient tested against all combinations of the other two. Though significant results were obtained for each individual level of each macronutrient against the others in combination, the difference between the confidence intervals was not significant. However, there was a clear trend: the optimum N levels were between 40 and 80 kg ha-1; optimum P level was 0 (the Control) and optimum K levels were between 100 and 200 kg ha-1. Tests of handling during harvest, storage, and planting yielded additional useful information for small scale commercial farmers. The optimal harvest time is May, when the false stem and leaves are senescing and yellow, but still upright and visible. Harvest is facilitated by moistening the soil to minimize breaking off of tuberous roots, with simple field washing to remove compacted soil highly recommended. Harvested corms and tuberous roots should be stored under air-restricted, cool conditions because the tuberous roots contain high moisture and will shrivel quickly when left exposed to air, and excessively dried corms will eventually die. Senesced mother corms should be discarded at harvest. Corms are genetically preprogrammed to shoot, so should be planted in September in soft soil, with 1-2 cm of soil coverage. The studies provide a framework for developing the basic agronomy for the domestication and commercial crop production of an endangered medicinal plant species. / Thesis (M.Sc.Agric.)-University of KwaZulu-Natal, Pietermaritzburg, 2011.

Submitted in complete fulfillment for the Degree of Master of Technology: Biotechnology, Durban University of Technology, 2013. / The biosynthesis of NPs has many advantages over the tedious, expensive and toxic physical and chemical methods of synthesis. Plants are stocked with valuable metabolites that are capable of reducing metal salts to form NPs. In this study, aqueous leaf extracts of A. dubius, G. perpensa, C. roseus and C. triloba were reacted with AgNO3 and HAuCl4 to determine the plants reducing abilities and hence synthesis of Ag and Au NPs capabilities. The synthesis reactions were carried out at different temperatures and extract concentrations for optimization. The goal was to form NPs within the specific wavelength range. Polar solvents: methanol and ethyl acetate extractions were carried out at the optimized conditions to evaluate the best solvent for the extraction of phytochemicals from the plants. The plant leaf extracts that were successful (A. dubius, G. perpensa and C. triloba) in synthesizing NPs were then micropropagated to form callus cultures. The reducing abilities of these callus cultures extracts were determined by varying temperature and concentration parameters. Characterization of the NPs formed by the different extracts was performed using UV-vis, TEM and FTIR. UV-vis spectrophotometry was used as a confirmatory as well as characterizing tool. TEM analysis was able to provide a description on the size and shape of the NPs whereas FTIR provided information on the biomolecules responsible for synthesis and capping of NPs. The stability of the NPs was determined by UV-vis scans over a period of 30 days which allowed observation of the alteration in peak shape and absorbance and hence condition of particles. Phytochemical tests were performed on the leaf extracts of the four plants to elucidate possible phytochemicals responsible for the reduction of metal salts. Antibacterial activity of the NPs was evaluated by using the disk diffusion assay and MICs were determined by the broth dilution method against pathogenic bacteria. A. dubius, G. perpensa and C. triloba were capable of synthesizing Ag NPs and Au NPs which were indicated by yellowish orange and reddish purple colour changes respectively. G. perpensa was able to spontaneously form Ag and Au NPs without any addition of heat whereas A. dubius and C. triloba required heat to form Au NPs. As the temperature of the reactions increased, the absorbance and possibly the number of NPs produced, increased. When the concentration of the extract was doubled, the absorbance was seen to decrease. C. roseus did not produce any Ag or Au NPs with any of the leaf extracts. Only A. dubius and C. triloba callus extracts were investigated for NP synthesis and it was found that A. dubius callus extracts were unsuccessful in synthesizing NPs and C. triloba callus extracts were able to form unstable Ag and Au NPs. The spherical Ag NPs that were formed from aqueous extracts of A. dubius were slightly larger than the methanolic Ag NPs. The Ag NPs produced by G. perpensa were in the same size range for aqueous and methanolic extracts. C. triloba Ag NPs formed from the methanolic extract were closer in size to A. dubius aqueous Ag NPs but the C. triloba aqueous extract produced much larger Ag NPs than the other extracts. The Ag NPs produced from A. dubius aqueous and methanolic extracts as well as C. triloba methanolic extracts exhibited the longest stability of 30 days. Ag NPs from G. perpensa aqueous extracts had the least stability. G. perpensa did not form any hexagonal Au NPs and the spherical and triangular Au NPs were smaller unlike in A. dubius and C. triloba Au NPs. The Au NPs formed by the aqueous extracts of A. dubius and C. triloba were larger in comparison to their methanolic counterparts. The Au NPs produced from G. perpensa aqueous and methanolic extracts as well as A. dubius and C. triloba methanolic extracts exhibited the longest stability of 30 days. Au NPs were stable for longer in comparison to Ag NPs. FTIR provided evidence that Ag and Au NPs have a chemical bond with the amide group in amino acids. However the intensities of biomolecules for Au NPs are more pronounced compared to the Ag NPs. It was also found that the Ag NPs synthesized by methanolic leaf extracts have slightly higher intensities than Ag NPs synthesized from aqueous leaf extracts. Phytochemical screening showed the absence of tannins in the C. roseus leaf, A. dubius and C. triloba callus extracts and presence in the other three plants. C. triloba methanolic extract Ag NPs showed the highest activity against Gram-positive S. aureus. Aqueous and methanolic Ag NPs from G. perpensa and C. triloba as well as A. dubius methanolic Ag NPs had activity against all fourteen bacteria. A. dubius aqueous Ag NPs had no activity against Enterobacter spp. and a strain of Klebsiella pneumoniae. G. perpensa Ag NPs had better antibacterial activity and lower MICs against Gram-positive and Gram-negative pathogenic bacteria compared to A. dubius and C. triloba. There was no antibacterial activity seen with Au NPs. The size and shape of NPs are the keys to their biomedical properties. Green synthesis of NPs is a feasible way for the future. This study showed that NPs can be synthesized very easily and economically. A key finding of this study is that different plants produce varying sizes and aggregation of NPs. / National Research Foundation

This study aimed to evaluate the antimicrobial efficacy of medicinal hemp plant extracts to determine the antibacterial effects of indigenous Sansevieria species and exotic Cannabis sativa phytotherapy varieties. This study also assessed whether aqueous o

<p>Since Helichrysum is known by the indigenous people of Africa for therapeutic properties, such as against colds, flu and wounds, the aim of this study was to focus on the patulum species found predominantly in the Western Cape region of South Africa and by means of isolation and identification of the plant constituents, be able to relate the therapeutic activity on the basis of literature precedents, to the compounds extracted.</p>

Neobeguea mahafalensis Leroy. and Cedrelopsis grevei Baill. are the two Madagascan species which were investigated in this work. Neobeguea mahafalensis Leroy. belongs to the Neobeguea genus of the Meliaceae family and is a plant unique to Madagascar. It is commonly referred to as "Handy" by the native people of Madagascar, who use it as a medicinal plant. The stem-bark of N mahafalensis which has been analysed in this work, was collected from the dry, thorny forests of the deep south of Madagascar. Most species found in this region are unique in the world and are highly specialised in adapting to the very dry climate. The hexane extract was found to yield a limonoid (compound I) which has not been previously reported as a natural product. The known pentacyclic triterpenoid, j3-amyrin (compound II) and stigmasterol (compound III), were also isolated. Cedrelopsis grevei Bail!. is one of seven species of the genus Cedrelopsis which are confined to Madagascar. This species, commonly referred to as "Katrafay" by the Madagascan people, has undergone intensive chemical investigation as prior inclusion ofthis species in the Meliaceae family has always been questionable. The South African species Ptaeroxylon obliquum (Thung.) Radlk., is a member of the Ptaeroxylaceaefamily which is found to be so chemically similar to Cedrelopsis that the latter has been placed in the Ptaeroxylaceae family. The stem bark of Cedrelopsis grevei was obtained from the dry southern part of Madagascar and yielded a variety of chromones and coumarins, as well as stigmasterol (compound III) and the pentacyclic triterpenoid, j3-amyrin (compound II). Two chromones were isolated from Cedrelopsis grevei, namely ptaeroxylinol (compound IV) and ptaeroglycol (compound V). Ptaeroglycol has been previously isolated _from this species as well as from Ptaeroxylon obliquum whereas ptaeroxylinol has only byen isolated from Ptaeroxylon obliquum. Six coumarins were isolated from Cedrelopsis grevei in tillS study, all of which were 6,7-dioxygenated coumarins. These included the known compounds, scoparone (compound VI), O-methylcedrelopsin (compound VIII), norbraylin (compound X) and cedrelopsin (compound IX), as well as compound VII and compound XI which . have not been reported previously. No limonoids were isolated from this species in this investigation. / Thesis (M.Sc.)-University of Natal, 1997.

Bulbs of Scilla natalensis Planch, Scilla nervosa (Burch.) Jessop, Scilla dracomontana Hilliard and Burt and Scilla kraussii Bak. (Hyacinthaceae) were investigated. The plants are widely used by the local African people for a variety of ailments that inflict them and their livestock. Plant material was harvested in different localities i.e. KwaZulu-Natal (KZN) and Mpumalanga (Mpl). The bulbs have been found to contain homoisoflavonoids and stilbenoids. Ten homoisoflavonoids and two stilbenoids were isolated. Of the ten homoisoflavonoids isolated, nine were of the 3-benzyl-4-chromanone type while one was a 3-benzylidene-4-chromanone. Four of the 3-benzyl-4-chromanones were found to be novel compounds while others were recognised as having been reported before from other genera within the family Hyacinthaceae viz., Eucomis and Muscari. The 3-benzylidene-4-chromanone type compound isolated was also found to be a known compound. The stilbenoids, on the other hand, are reported for the first time in this genus although they seem to have a wide distribution in the plant kingdom. The structures of the isolated compounds were elucidated using spectroscopic methods. / Thesis (M.Sc.)-University of Natal, Durban, 1998.

The research presented in this study demonstrates the critical role that organic synthesis plays in natural product chemistry. The biological activity demonstrated by 2-methyl-6-(3-methyl-2- butenyl)benzo-1,4-quinone prompted an investigation into the synthesis of this compound. This natural product showed significant activity against Staphylococcus epidermidis. Therefore the aim of this study was to synthesise 2-methyl-6-(3-methyl-2-butenyl)benzo-1,4- quinone and structural analogues. The regioselective synthetic route formulated for the synthesis of 2-methyl-6-(3-methyl-2- butenyl)benzo-1,4-quinone involved five steps. Different strategies towards the synthesis of this compound were investigated. The regioselective C-alkylation step was proving to be the most challenging. The synthetic strategies investigated included carbon alkylation of a phenoxide, directed-o-metallation, metal-halogen exchange and copper(II) Grignard-type metal halogen exchange. Problems were encountered with regioselectivity when carbon alkylation of a phenoxide was employed for the o-prenylation of o-cresol. The C-prenylated isomer was formed along with the O-prenylated isomer. When the reaction temperature was lowered, the yield of the desired C-prenylated isomer improved, whereas the yield of O-prenylated isomer declined. Although the reaction was performed under different conditions, the formation of the O-prenylated isomer could not be prevented. Therefore, another synthetic strategy was considered. The directed-o-metallation reaction was subsequently employed because of the associated regioselectivity. Unfortunately the desired product was not obtained when this method was employed. The reaction was attempted using different conditions, but the product could not be isolated. Since the directed-o-metallation protocol did not yield the desired results, another method was considered. Therefore, a metal-halogen exchange reaction was employed. The metal-halogen exchange transformation was preceded by the preparation of the o-brominated precursor. Regioselectivity-related problems were initially encountered during the synthesis of the obrominated precursor. The o-brominated isomer was formed in a 1:1 ratio with the pbrominated isomer. Further investigation led to a synthetic protocol that afforded the desired o-brominated isomer in a better yield. The metal-halogen exchange transformation was subsequently attempted, but the product was obtained in an unsatisfactory yield. Therefore, another method was employed in an effort to achieve regioselective C-alkylation with a better yield. Copper(II) Grignard-type metal-halogen exchange was successfully employed to achieve regioselective C-alkylation in good yield. The subsequent step was the deprotection, although problems were encountered, it was eventually achieved. The final step was the oxidation to obtain the desired compound, 2-methyl-6-(3-methyl-2-butenyl)benzo-1,4- quinone. The same procedure was successfully applied in the synthesis of structural analogues 2-isopentyl-6-methylbenzo-1,4-quinone, 2-(3,7-dimethylocta-2,6-dienyl)-6-methyl-1,4- benzoquinone and 2-(3,7-dimethyl-octyl)-6-methyl-1,4-benzoquinone. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2010.

Ledebouria zebrina and Scilla natalensis Planch were the two species investigated in this work. Ledebouria zebrina belongs to the Hyacinthaceae (Liliacea sensu lato) and to this date, the chemical composition of this species has not been investigated. Members of this family are found in southern Africa. The Ledebouria genus was formerly classified as part of the Scilla genus from which a large member of naturally occuring oxygen heterocycles known as homoisoflavanones have been isolated. In this work the bulbs of L. zebrina were investigated and five compounds were isolated. Three compounds were of the homoisoflavanone type while the remaining two belong to the eucosterol type triterpernoids. Scilla natalensis Planch also belongs to the Hyacinthaceae family. Previous chemical investigations of the bulbs of this plant yield two homoisoflavanones of the 3-benzyl-4- chromanone type. Members of this family are mostly found in the Eastern parts of the country, ranging from the Eastern Cape to Mpumalanga province including Lesotho and Swaziland. The bulbs of this plant were investigated and this yielded ten compounds. The structures of the isolated compounds were elucidated using spectroscopic methods. / Thesis (M.Sc.)-University of Natal, Durban, 2001.

Two species belonging to different families were investigated, Eucomis montana from the Hyacinthaceae and Agapanthus inapertus from the Agapanthaceae. To date no previous chemical investigation on Eucomis montana has been reported. Eucomis species are routinely harvested, processed and sold for the treatment of various ailments ranging from toothache, gastro-intestinal ailments, pain-producing ailments and venereal and urinary diseases. Members of the genus have shown to contain steroidal compounds and homoisoflavonoids. In this work one nortriterpenoid, a eucosterol type derivative and eleven homoisoflavonoids belonging to four classes, the 3-benzyl-4-chromanone, the 3-benzyl-3-hydroxy-4-chromanone, the 3-benzylidenyl-4-chromanone and the scillascillin type were found in the bulbs of Eucomis montana. Agapanthus species are also used by a number of African tribes medicinally. The bulbs and rhizomes of this family have been reported to contain steroidal saponins and sapogenins. In this work the roots of Agapanthus inapertus have been investigated and a tignan precursor and a lignan have been found. Structures of the compounds isolated were determined using spectroscopic techniques. / Thesis (M.Sc.)-University of Natal, Durban 2003.

Ph.D. (Botany) / The most well-known tonic plants in South Africa have been used traditionally for the treatment of a great variety of ailments but aspects of their ethnobotany and chemistry remain poorly studied. Possible relationships between their ethnobotany and pharmacology are mostly speculative. In this study, literature reviews of the ethnobotany of these plants were combined with phytochemical screening studies and bitterness taste testing results in order to establish constituent patterns which may contribute to a scientific rationale for the claimed tonic (stimulating) properties of these plants. The tonic concept and definitions of terms associated with it are often used incorrectly and ambiguously. An analysis of literature on the traditional healing systems across the globe was used to establish the historical and cultural aspects relevant to tonics. This analysis revealed that sickness/illness is usually considered to be a result of imbalance in many cultures, whether this imbalance is between the patient and the environment or due to a lack of homeostasis in the body. In several healing cultures substances or mixtures of substances are used to rectify these imbalances through proposed effects on several bodily systems concurrently. According to some cultures, as in Eastern and Indian traditional medicine, tonic plants are considered superior to other medicinal plants in that they impart health, strength and a general sense of well-being, as well as being prophylactic. This definition of a tonic plant is consequently broad, but excludes plants merely used as multipurpose medicines. Where these tonics exhibit a specific mode of action, further classification is required, i.e. as bitter, adaptogenic, alterative, adjuvant or stimulant tonics. The South African traditional tonic plants studied were Agathosma species (Rutaceae), Aloe species (Asphodelaceae), Arctopus species (Apiaceae), Artemisia afra (Asteraceae), Balanites maughamii (Balanitacae), Dicoma species (Asteraceae), Harpagophytum procumbens (Pedaliaceae), Hypoxis hemerocallidea (Hypoxidaceae), Muraltia heisteria (Polygalaceae), Sutherlandia species (Fabaceae), Vernonia oligocephala (Asteraceae), Warburgia salutaris (Canellaceae), Withania somnifera (Solanaceae) and Ziziphus mucronata (Rhamnaceae). A detailed compendium of medicinal applications was compiled following a thorough, in-depth scrutiny of the historical and medicinal ethnobotany of each of these species. Such ethnobotanical data is important in understanding the cultural aspects of healing in southern Africa, and provides valuable direction and focus with regards to the phytochemical and pharmacological research of these plants.