Thesis (MSc)--University of Stellenbosch, 2004. / ENGLISH ABSTRACT: Thirteen Sulfobacillus strains from different geographical locations and two Alicyclobacillus strains were included in this study. These organisms proved to be moderately thermophillic (two different sets of optimal temperatures of 45°C and 55°C were found), Gram-positive, endospore forming bacteria. The pH optima of the strains tested was pH 2.5 and the pH range lay between pH 1.5 and pH 5.0. It was established that some strains of Sulfobacillus had the capacity for anaerobic growth when using ferric iron as an electron donor. It was determined that S. thermosuljidooxidans was the species found within South African biooxidation plants. Plasm ids were identified within strain 611 (S. thermosuljidooxidans) isolated from a Billiton commercial plant. The sample of Sulfobacillus strains used in this study could clearly be divided into two groups based on the analysis of their 16S rRNA gene sequences as well as the number of ribosomal (rm) operons present as determined by Southern hybridization. A system for the convenient identification of Sulfobacillus species was developed using several of the techniques employed in this study. Preliminary identifications can be obtained by restriction enzyme digestion of the PCR amplified 16S rRNA gene. Confirmation of this placement can be done by comparison of the 16S - 23S rRNA spacer region amplification band sizes. Once the preliminary identification has been completed it is possible to place the isolate in the correct species by making use of the differences in sugar utilization that the species exhibit. The more laborious method of 16S rRNA sequence comparisons can be undertaken if there is still any uncertainty as to which species an isolate belongs to. Phylogenetic results obtained from the 16S rRNA gene sequence indicates that the genus Sulfobacillus should probably be divided into two individual genera. Further information gathered from the phylogenetic comparisons indicates that strain Riv-14 previously assigned to S. ambivalens is more closely related to S. montseratensis. Data obtained from 16S - 23S rRNA spacer region analysis confirms this result. Future work includes the use of DNA-DNA hybridization studies and mol% G+C ratio's in order verify the presence of two distinct genera as well as placing Riv-14 within the correct species. / AFRIKAANSE OPSOMMING: Dertien isolate van die genus Sulfobacillus afkomstig van geografies verskillende areas en twee isolate van die genus Alicyclobacillus is in die studie ingesluit. Hierdie organismes het gewys dat hulle gematigde termofiele (twee verskillende groepe met optimale temperature van 45°C en 50°C elk was waargeneem), Gram-positiewe, endospoorvorrnende organismes is. Die pH optima van die isolate was pH 2.5 en die reeks van pH waar groei moontlik was het tussen pH l.5 en pH 5.0 gelê. Dit was bewys dat sekere van die Sulfobacillus isolate oor die vermoë beskik het om anaerobies te respireer deur ferri yster (Fe3+) as elektron akseptor te gebuik. Dit was bepaal dat S. thermosulfidooxidans die spesies is wat teenwoordig was in die bio-oksidasie reaktors in Suid Afrika. Plasmiede vanuit die isolaat 611 (s. thermosulfidooxidans) afkomstig vanuit 'n Billiton komersieële reaktor, is geidentifiseer. Die toetsmonster van Sulfobacillus isolate gebruik in hierdie studie het duidelik daarop gewys dat daar twee groepe binne Sulfobacillus is. Hierdie stelling is gebaseer op data afkomstig van die analiese van die 16S rRNA volgorde asook die aantal ribosomale (rm) kopieë teenwoordig soos bepaal deur Southern klad eksperimente. 'n Sisteem vir die maklike identifikasie van Sulfobacillus spesies is ontwerp deur van verskeie tegnieke, soos in hierdie studie toegepas, gebruik te maak. Aanvanklike identifikasie kan verkry word deur gebruik te maak van restriksie ensiem vertering van PKR geamplifiseerde 16S rRNA geen. Hierdie plasing van die isolaat kan bevestig word deur die grootte van die 16S - 23S rRNA intergeniese amplifikasie produkte te vergelyk. Sodra die aanvanklike plasing van die isolaat voltrek is, kan daar van die verskille in die vermoëns van die spesies om sekere suikers the benut, gebruik gemaak word om die isolaat binne die regte spesies te plaas. Die meer werksintensiewe metode van 16S rRNA volgorde vergelyking kan gebruik word indien daar enige onsekerheid is oor by watter spesies die isolaat hoort. Filogenetiese resultate verkry van die vergelyking van die 16S rRNA geen volgorde dui daarop aan dat die genus Sulfobacillus waarskynlik uit meer as een genus bestaan. Die filogenetiese data dui verder daarop dat die isolaat Riv-14 wat as 'n S. ambivalens geklassifiseer is, nader verwant is aan die spesies S. montseratensis. Data verkry vanaf die 16S - 23S intergeniese gebied analiese bevestig hierdie resultaat. Toekomstige werk sluit DNA-DNA hibridisasie en mol% Gte ratio eksperimente in om sodoende die teenwoordigheid van meer as een genus sowel as die plasing van Riv-14 in die korrekte spesies te bevestig.

Thesis (PhD)--University of Stellenbosch, 2004. / ENGLISH ABSTRACT: Plants cannot avoid stress and must therefore be capable of rapidly responding to extreme environmental changes. An inability to control and regulate the photosynthetic process during stress conditions will lead to the formation of highly reactive oxygen species that concomitantly causes photo-oxidative damage to the pigments and proteins of the photosynthetic apparatus. Since light is the primary source of energy for the photosynthetic process, it is clear that plants are continuously required to balance the light energy absorbed for the photochemical reactions against photoprotection in a dynamic way in order to survive. Carotenoids are precursors of abscisic acid, but more importantly structural components of the photosynthetic apparatus. During photosynthesis carotenoids function as accessory light-harvesting pigments, and also fulfil a photoprotective function by quenching the reactive molecules formed during conditions that saturate the photosynthetic process. Due to the importance of carotenoids to plant fitness and human health (as Vitamin A precursors) this study has attempted to isolate and characterise genes that are directly, or indirectly involved in carotenoid biosynthesis in Vitis vinifera. In total eleven full-Iength- and eight partial genes have been isolated, cloned and sequenced. These genes can be grouped into the following pathways: (i) the 1- deoxy-D-xylulose 5-phosphate (DOXP)/2-C-methyl-D-erythritol 4-phosphate (MEP) pathway (i.e. the plastidic isopentenyl diphosphate biosynthetic pathway); (ii) the mevalonate pathway (i.e. the cytosolic/mitochondrial IPP biosynthetic pathway); (iii) the carotenoid biosynthetic pathway; (iv) the abscisic acid biosynthetic pathway (as a degradation product of carotenoids); and general isoprenoid biosynthetic pathways (as precursors of carotenoids). The full-length genes (i.e. from the putative ATG to the STOP codon) of DOXP synthase (DXS), 4-hydroxy-3-methylbut-2-enyl diphosphate reductase (lytB), IPP isomerase (IPI), 3-hydroxy-3-methylglutaryl coenzyme A synthase (HMGS), phytoene synthase (PSY), Iycopene ~-cyclase (LBCY), ~-carotene hydroxylase (BCH), zeaxanthin epoxidase (lEP), 9-cis-epoxy carotenoid dioxygenase (NCED), farnesyl diphosphate synthase (FPS) and geranylgeranyl diphosphate synthase (GGPS) have been isolated from cDNA. In addition, the full-length genomic copy and putative promoters of DXS, PSY, LBCY, BCH, NCED and lEP have also been isolated from genomic DNA by the construction and screening of sub-genomic libraries. Alignments of the genomic copies of these genes to the corresponding cDNA sequences have provided useful information regarding the genomic organisation of these genes, including the intron-exon junction sites in V. vinifera. The copy number of the DXS, PSY, LBCY, BCH, NCED and lEP encoding genes in the Vitis genome have been determined. DXS, PSY, BCH and lEP are single copy genes, whereas LBCY and NCED have two and three copies, respectively. The transcriptional activity of the putative promoters of six of the isolated genes (i.e. DXS, PSY, LBCY, BCH, lEP and NCED) were tested with a transient reporter gene assay. None of the putative promoters tested showed any transcriptional activity of the reporter gene. The transcription of these genes, has however been shown using northern blot analysis and/or RT-PCR. Preliminary expression profiles for PSY, LBCY, BCH, and lEP were determined in different plant organs and the expression of these genes was generally higher in photosynthetically active tissues. The expression of these genes following different treatments (abscisic acid, NaCI and wounding) was also assayed. The functionality of five of the isolated full-length genes (IPI, GGPS, PSY, LBCY and BCH) has been shown in a bacterial colour complementation assay. In silica analysis of the predicted protein sequences of all eleven isolated genes revealed that they are conserved and share a high degree of homology to the corresponding proteins in other plant species. The sequences were further analysed for conserved domains in the protein sequences, and these proteins typically demonstrated similar domain profiles to homologues in other species (plant, bacteria and algae). The predicted protein sequences were further analysed for transit peptides, the presence of which would provide evidence for the sub-cellular localisation of the mature peptides. Since these genes are involved in biosynthetic pathways that are active in discrete organelles, the sub-cellular localisation of most of these proteins is known. The carotenoid biosynthetic genes (PSY, LBCY, BCH and ZEP), the abscisic acid biosynthetic gene, NCED, as well as the DOXP/MEP pathway genes (DXS, lytB and IPI) were all localised to the chloroplast. The mevalonate pathway gene, HMGS, was localised to both the cytosol and the mitochondria, and the general isoprenoid precursor genes, FPS and GGPS, were localised to the cytosol and the chloroplast, respectively. All these results are in agreement with the localisation of the respective pathways. In order to increase our understanding of carotenoid biosynthesis and functions in plants, we constitutively overexpressed one of the isolated genes (BCH) in the model plant, Nicotiana tabacum. Plants expressing the BCH gene in the sense orientation maintained a healthy photosynthetic rate under stress conditions that typically caused photoinhibition and photodamage in the untransformed control plants. This result was inferred using chlorophyll fluorescence and confirmed using CO2 assimilation rates and stomatal conductance. Chlorophyll fluorescence measurements indicated that the photo protective non-photochemical quenching ability of the BCH-expressing plants increased, enabling the plants to maintain photosynthesis under conditions that elicited a stress response in the untransformed control plants. An integral photosynthetic protein component, the D1 protein, was specifically protected by the additional zeaxanthin in the BCH sense plants. Plants expressing an antisense BCH proved the converse, i.e. lower levels of BCH resulted in decreased zeaxanthin levels and made the transgenic plants more susceptible to high-light induced stress. These results have shown the crucial role of carotenoids (specifically the xanthophylls) in the photoprotective mechanism in plants. The increased photoprotection provided by the BCH expressing plants suggests that the scenario in plants is not optimal and can be improved. Any improvement in the photoprotective ability of a plant will affect both the fitness and productivity of the plant as a whole and will therefore find application in a number of crop plants on a global scale. This study has resulted in the successful isolation and characterisation of genes involved in the direct, or indirect, carotenoid biosynthetic pathways. The further study and manipulation of these genes in model plants will provide useful insights into the physiological role of specific carotenoids in photosynthesis and in plants as a whole. / AFRIKAANSE OPSOMMING: Plante het nie die vermoë om stres te ontwyk nie en moet dus vinnig op veranderinge in hulomgewingstoestande kan reageer. Indien hulle nie die fotosinteseproses kan kontroleer en reguleer tydens streskondisies nie, sal dit tot die vorming van hoogs reaktiewe suurstofspesies lei, wat beide die pigmente en proteiene van die fotosintetiese apparaat sal beskadig. Lig is die primêre energiebron vir fotosintese en daarom is dit noodsaaklik dat plante deurgaans 'n dinamiese balans tussen fotosintese en fotobeskerming moet handhaaf. Karotenoiëde is voorlopers vir die vorming van absisiensuur, maar meer belangrik vir die plant, ook integrale komponente van die fotosintetiese apparaat. Tydens fotosintese word karotenoiëde vir die opneem van lig benodig, terwyl dit ook die fotosintetiese apparaat beskerm wanneer lig 'n versadigingspunt bereik vir fotosintese. Weens die belang van karotenoiëde vir plant- en menslike gesondheid (as Vitamiene A voorlopers), het hierdie studie beoog om gene te isoleer en karakteriseer wat direk of indirek 'n rol in karoteenbiosintese in Vitis vinifera speel. Elf vollengte- en agt gedeeltelike gene is geïsoleer, gekloneer, en gekarakteriseer. Hierdie gene kan in die volgende biosintetiese paaie gegroepeer word: (i) die 1- deoksi-D-xilulose 5-fosfaat (DOXP)/2-C-metiel-D-eritritol-4-fosfaat (MEP) pad (d.w.s. die plastiediese isopenteniel difosfaat biosintetiese pad); (ii) die mevalonaat pad (d.w.s. the sitosoliese/mitokondriale IPP biosintetiese pad); (iii) die karotenoiëd biosintetiese pad; (iv) die absisiensuur biosintetiese pad (as 'n afbraak produk van karotenoiëde) en die algemene isoprenoïed bisintetiese paaie (as voorlopers van karotenoiëde ). Die vollengte gene (d.w.s. vanaf die geskatte ATG tot die STOP kodon) van DOXP-sintase (DXS), 4-hidroksi-3-metielbut-2-eniel difosfaatreduktase (lytB), IPPisomerase (IPI), 3-hidroksi-3-metielglutariel koensiem A sintase (HMGS), fitoeën sintase (PSY), likopeen p-siklase (LBCY), p-karoteen hidroksilase (BCH), zeaxantien oksidase (ZEP), 9-cis-epoksi karotenoiëd dioksigenase (NCED), farnesiel difosfaat sintase (FPS)en geranielgeraniel difosfaat sintase (GGPS) is met behulp van. RTPKR vanaf eDNA geïsoleer. Die vollengte genomiese kopieë en die verwagte promotors van die DXS, PSY, LBCY, BCH, NCED and ZEP gene is ook geïsoleer d.m.v. die opstel en sifting van subgenomiese biblioteke. Vergelykende analises van die genoom- en eDNA kopieë het insiggewende data oor die genomiese rangskikking van die gene, insluitende die intron-ekson setels in V. vinifera gelewer. Die kopiegetalle van DXS, PSY, LBCY, BCH, NCED en ZEP is bepaal. DXS, PSY, BCH en ZEP is in die Vitis-genoom as enkel kopieë teenwoordig, terwyl LBCYen NCED twee en drie kopieë, repektiewelik, beslaan. Die transkipsionele aktiwiteit van die verwagte promotors van ses van die geïsoleerde gene (naamlik DXS, PSY, LBCY, BCH, ZEP en NCED) is d.m.v. 'n tydelike verklikkergeentoets ondersoek. Geeneen van die promotors het die transkripsie van die verklikkergeen bemiddel nie. Die transkripsie van die gene is egter wel bewys deur van northernhibridisasies en/of RT-PKR gebruik te maak. Die promotors van hierdie gene kan dus as transkipsioneel aktief beskou word. Voorlopige uitdrukkingsprofiele van PSY, LBCY, BCH, en ZEP is in verskillende plantorgane bepaal; die profiele was deurgaans hoër in fotosinteties aktiewe weefsels. Die uitdrukkingsprofiele van die gene is verder ook in reaksie op verskillende induktiewe behandelings (absisiensuur, NaCI en beskadiging) bepaal. Vyf van die vollengte gene (IPI, GGPS, PSY, LBCYen BCH) is funksioneel bewys in 'n bakteriese funksionele kleurkomplementasiesisteem. In silico analises van die afgeleide proteïene van al elf geïsoleerde gene het 'n hoë vlak van homologie met ooreenstemende proteiene van ander plantspesies getoon. Gekonserveerde domeine is ook in die proteïensekwense van die geïsoleerde gene teenwoordig. Hierdie proteïene het deurgaans dieselfde domeinprofiele vertoontoon as homoloë in ander spesies (bakterieë, alge en plante). Die sub-sellulêre teikening van die gene kon voorspel word deur die seinpeptiede in die proteiensekwense te eien. Aangesien hierdie gene betrokke is by biosintetiese paaie wat in diskrete kompartemente plaasvind; is die sub-selluiêre lokalisering van hierdie proteïene voorspelbaar. Die karotenoïed biosintetiese gene (PSY, LBCY, BCH en ZEP), die absisiensuur biosintetiese geen, NCED, sowel as die DOXP/MEP pad se gene (DXS, lytB en IPI) kom almal in die chloroplast voor. Die mevalonaatpadgeen, HMGS, word na beide die sitosol en die mitokondria geteiken, terwyl die algemene isoprenoïed voorlopergene, FPS en GGPS, onderskeidelik na die sitosol en die chloroplast geteiken word. Die verkreë voorspellings stem met die lokalisering van die biosintetiese paaie in die selooreen. Om ons kennis rakende karotenoïed biosintese en veral hulle funksie(s) in plante te verbreed, het ons een van die geïsoleerde gene, BCH, in die model plant, Nicotiana tabacum, konstitutief ooruitgedruk. Plante wat die BCH geen in die "sense" orientasie uitgedruk het, kon normale fotosintetiese aktiwiteit handhaaf onder kondisies wat foto-inhibisie en foto-osidatiewe skade in die ongetransformeerde kontrole plante veroorsaak het. Hierdie resultaat is met chlorofil fluoresensie analises aangetoon terwyl dit met CO2 assimilasie- en huidmondjie geleidingseksperimente bevestig is. Chlorofil fluoresensie metings het aangetoon dat die beskermingsvermoë van die transgeniese plante verhoog is, en dit dan die plante in staat stelom fotosintetese te handhaaf onder streskondisies van hoë lig. Proteïen analises het aangetoon dat 'n integrale fotosintetiese proteien, die 01 proteïen, word veral deur die verhoogde zeaxantien vlakke in die BCH transgeniese plante beskerm. Plante wat verminderde zeaxantien vlakke gehad het, weens die konstitutiewe ooruitdrukking van die BCH geen in die anti-"sense" orientasie, het die teenoorgestelde bewys. Met ander woorde. laer BCH vlakke (en dus laer zeaxantien vlakke) het tot plante wat meer vatbaar was vir hoë lig geïnduseerde stress gelei. Hierdie resultate het die essensiële beskermende rol wat karotenoiede tydens fotosintese speel, uitgelig. Die vermoë om hierdie beskermende meganisme te manipuleer in transgenies plante het aangetoon dat die sisteem in plante, alhoewel effektief, nie optimaal is nie. Enige verbetering in 'n plant se inherente vermoë om streskondisies te weerstaan sal die plant se algemene gesondheid en dus produktiwiteit beïnvloed. As sulks sal hierdie in meeste gewasspesies toepassing vind. Hierdie studie beskryf die isolering en karakterisering van gene wat direk, of indirek, by karotenoïedbiosintese betrokke is. Verdere studies, en veral die manipulering van hierdie gene in model plante, sal die fisiologiese rol van spesifieke karotenoïeede in fotosintese, en die plant as 'n geheel, ontrafel.

Thesis (PhD (Botany and Zoology))—University of Stellenbosch, 2009. / The genus Oxalis forms a major part of the flora of southern Africa, in particular the Cape Floristic Region (CFR) at the southwestern tip of the continent, but the current taxonomy is outdated and ecological knowledge of the lineage is sadly incomplete. In this thesis I set out to address several aspects of Oxalis systematics that urgently require attention. Firstly, the current macro-morphological taxonomy requires phylogenetic testing, as it is acknowledged to be incomplete and artificial. I address this need by providing a DNA sequence-based phylogeny of three markers, using three different inference methods, for nearly three quarters of the indigenous species. This phylogeny confirmed both the monophyly of the southern African taxa, and the artificiality of the current classification system. It is congruent with previous sequence-based reconstructions of smaller groups of southern African Oxalis species, and with the palynological classification proposed for the genus. Secondly, previous phylogenetic work on the southern African members could not resolve basal relationships within the southern African clade. I attempt to address this problem by sequencing three extra chloroplast markers for a select group of taxa, followed by separate and combined (total evidence) molecular phylogenetic analyses. This approach did increase resolution at the base of the southern African lineage, but many clades still showed poor resolution and support despite the use of more than 7 000 bases of sequence data. Resolving these clades within the southern African Oxalis phylogeny remains a challenge, and should prove a fertile field for future research. Thirdly, the ages (and thus duration of presence) of many Cape plant lineages within the CFR are of major interest, given that the CFR represents a global biodiversity hotspot. The age of the genus in the Cape is estimated by analyzing combined sequence data for all sampled taxa under both a Bayesian Relaxed Clock and a semiparametric Penalised Likelihood method, using calibration points inferred from Relaxed Clock analyses of the entire order Oxalidales, for which fossil data are available. In an attempt to account for known problems with divergence time estimation, I explored the potential bias introduced by method used, marker genome source and different calibrations on the root. The results indicate substantial variation in the age of crown southern African Oxalis over a nearly twenty million year period, varying according to source data, calibration estimate and methodology employed in the reconstruction. Despite this major variability, all average estimates are older than iv 18 million years, which agrees with a growing body of evidence that there has been a gradual accumulation of floristic diversity in the CFR, rather than a rapid, recent burst of speciation. Fourthly, as the produced phylogenies conclusively show the artificial nature of the current taxonomy, I propose a new, almost completely different classification for southern African Oxalis taxa. Although a significant improvement, this classification is considered informal due to the complete disagreement between the old and proposed new taxonomies, poor resolution in some of the proposed lineages, and a need to confirm proposed groups (clades) with the identification of morphological synapomorphies. Potential synapomorphies for various clades are proposed and discussed, which should guide future research. Fifthly, the presence of bulbs in this genus is of great interest as a potential preadaptation for seasonally arid climates. The evolution of the bulbous habit in Oxalis is here explored for the first time. I address the sequence of major morphological character state changes leading to the suite of characters corresponding to the bulbous habit. The homology of basal leaf petioles, fleshy leaf scales and tunics is discussed, and it is shown that many bulb characters present in the southern African lineage are also found in the close relatives of this lineage, and are thus older than this lineage. The ecological and evolutionary implications of bulb geophytism in the CFR Oxalis are also discussed. Finally, I address certain taxonomic issues that arose during the course of this study. Co-authors and I describe the new species O. saltusbelli and O. ericifolia. We also clarify issues surrounding the tremendously variable group species O. flava and propose some nomenclatural changes and synonyms for related taxa. We also address the taxonomic position of the rare species O. purpurata, which was located too late in the course of this study to include in the main analyses.

published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

published_or_final_version / abstract / Ecology and Biodiversity / Doctoral / Doctor of Philosophy

published_or_final_version / abstract / Orthopaedics and Traumatology / Doctoral / Doctor of Philosophy

published_or_final_version / abstract / Chemistry / Master / Master of Philosophy

published_or_final_version / abstract / Obstetrics and Gynaecology / Master / Master of Philosophy

published_or_final_version / abstract / Pharmacology / Doctoral / Doctor of Philosophy

published_or_final_version / Surgery / Doctoral / Doctor of Philosophy