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Abstract The genus Pteronia consists of approximately 80 species which are widely distributed in southern Africa. For hundreds of years the indigenous people of southern Africa have turned to the earth in order to provide healing for their people. The genus Pteronia has been amongst the first species to be used by the San and Khoi-San people for treating infections and stomach ailments. Ten species were selected for the purpose of this report. The essential oils were isolated by using a Clevenger-type apparatus while the non-volatiles were extracted with acetone and methanol. The essential oils and extracts were assessed for antimicrobial activity. The disc diffusion assays included three Gram-negative bacteria; Escherichia coli, Yersinia enterocolitica and Klebsiella pneumoniae, three Gram-positive bacteria; Staphylococcus aureus, Bacillus subtilis and Bacillus cereus as well as one yeast; Candida albicans. Results indicated that the species were primarily active against Gram-positive organisms. The minimum inhibitory concentration of the ten most active species (essential oils and extracts) were determined using the microdilution method. The most promising activity was noted for P. fasiculata which had a MIC of 0.22 mg/ml against S. aureus, 0.39 mg/ml against B. cereus and 2.08 mg/ml against B. subtilis. The essential oils analysis by GC/MS revealed two chemotypes. In Pteronia pallens, P. empetrifolia and P. flexicaulis rare compounds, such as presilphiperfolol-7-ene, 7-α-(H)-silphiperfol-5-ene, 7-β-(H)-silphiperfol-5-ene, α-campholene aldehyde, silphiperfol-5-ene, camaroonan-7-α-ol, silphiperfol-7- β -ol, presilphiperfolan-9- α -ol and presilphiperfolan-8-ol (a major compound in Pteronia pallens) were recorded. A cluster analysis of the essential oil data indicated that individual collections of P. camphorata within a population were tightly clustered. Similarly, P. pallens sampled from three different localities were also united in the cluster analysis. These results suggest minimal within and between population variations for some of the species studied.

In the rubber industry, plasticizers for rubber compounds mainly consist of petroleum derivatives. Consequently, the rubber industry is in constant competition with many petroleum consumers. This competition places an economic strain on rubber companies such as HEXPOL RUBBER COMPOUNDING L.L.C. In order to alleviate this strain, natural oil alternatives to petroleum plasticizers are of novel research interest and are investigated in this thesis project.

Thesis (Ph.D.)--University of Delaware, 2006. / Principal faculty advisor: Richard P. Wool, Dept. of Chemical Engineering. Includes bibliographical references.

Thesis--Auburn University, 2009. / Abstract. Vita. Includes bibliographic references (p.120-131).

1. <i>Cis</i> unsaturated fatty acids were shown to inhibit porcine platelet aggregation in response to both collagen and thrombin. Fatty acids with a <i>trans</i> double bond had an anti-aggregatory effect on collagen-induced aggregation but this was significantly less than that observed with the <i>cis</i> equivalent and was diminished as the dose of agonist increased. Thrombin-induced platelet aggregation was unchanged or slightly potentiated by <i>trans</i> isomers. 2. Both the <i>cis</i> and <i>trans</i> isomeric acids inhibited collagen-induced TXB₂ production. The <i>trans</i> unsaturated fatty acids also inhibited TXB₂ production in response to thrombin, even though they did not inhibit thrombin induced platelet aggregation. 3. Unlike arachidonic acid, the <i>cis</i> and <i>trans</i> mono-unsaturated fatty acids were not rapidly incorporated into membrane phospholipids but modified platelet aggregation whilst in the free acid form. 4. Pre-incubation of platelets with either <i>cis</i> or <i>trans</i> delta 13, 18:1, selectivity inhibited the incorporation of radio-labelled arachidonic acid into membrane PS. 5. <i>Cis</i> and <i>trans</i> unsaturated delta 13, 18:1, inhibited the initial turnover of membrane PI in response to thrombin possibly by an inhibitory effect on PI-specific phospholipase C. After 5 minutes, however, the level of arachidonic acid released from both PI and PE was increased in the presence of the isomeric fatty acids. This may have been via a potentiation of the action of phospholipase A₂. 6. An increased release of arachidonic acid could result in the inhibition of aggregation if metabolised via the 12-lipoxygenase pathway, as the end products of this sytem have direct anti-aggregatory activity and inhibit the cyclo-oxygenase enzymes thus reducing TXA₂ synthesis. 7. <i>Cis</i> unsaturated fatty acids, which produce a greater level of membrane disruption than the <i>trans</i>, may lead to more efficient channelling of the released arachidonic acid in the direction of the lipoxygenase pathway, and thereby produce a greater inhibition of aggregation. The possibility remains that the <i>cis</i> isomers have another, as yet unidentified mechanism by which they inhibit platelet aggregation.

Graduation date: 1960