https://vital.seals.ac.za/vital/access/manager/Index ${session.getAttribute("locale")} 5 Assembly of full-length cDNA, and heterologous expression, of Nudaurelia B virus RNA https://vital.seals.ac.za/vital/access/manager/Repository/vital:3913 Wed 12 May 2021 23:37:14 SAST ]]> Analysis of the anti-cancer activity of novel indigenous algal compounds in breast cancer: towards the development of a model for screening anti-cancer stem cell activity https://vital.seals.ac.za/vital/access/manager/Repository/vital:3925 Wed 12 May 2021 23:30:20 SAST ]]> Development of an in-situ ß-D-Glucuronidase diagnostic moraxella-based biosensor for potential application in the monitoring of water polluted by faecal material in South Africa https://vital.seals.ac.za/vital/access/manager/Repository/vital:3947 Wed 12 May 2021 23:14:43 SAST ]]> Biosorption of precious metals from synthetic and refinery wastewaters by immobilized saccharomyces cerevisiae https://vital.seals.ac.za/vital/access/manager/Repository/vital:4071 Wed 12 May 2021 22:26:49 SAST ]]> Biological synthesis of metallic nanoparticles and their interactions with various biomedical targets https://vital.seals.ac.za/vital/access/manager/Repository/vital:4009 50%). Thus, it can be concluded that the cavities of apoferitin and GroEL acted as nanobiofactories for the synthesis and confinement of the size and shape of nanoparticles. Furthermore, the interior of these proteins provided a shielding effect for these nanoparticles and thus reduced/prevented their possible neurotoxic effect and confirmed safety in their method of production and application. The findings from this study would prove beneficial in the application of these nanoparticles as a potential drug/drug delivery vehicle for the prevention, treatment/management of diseases associated with these enzymes/proteins.]]> Wed 12 May 2021 22:22:09 SAST ]]> A study of petrol and diesel fuel blends with special reference to their thermodynamic propeties and phase equilibria https://vital.seals.ac.za/vital/access/manager/Repository/vital:4065 Wed 12 May 2021 20:35:39 SAST ]]> Function of a cloned polyphenolase in organic synthesis https://vital.seals.ac.za/vital/access/manager/Repository/vital:4042 Wed 12 May 2021 20:35:17 SAST ]]> Determination of the botanical composition of black rhinoceros (Diceros bicornis) dung using the rbcL gene as a molecular marker, and analysis of antioxidant and phenolic content of its browse https://vital.seals.ac.za/vital/access/manager/Repository/vital:4070 ethyl acetate > chloroform. The DPPH free radical scavenging activity of the methanol plant extracts increased in the order Brachylaena elliptica > Plumbago auriculata > Grewia robusta > Azima tetracantha. Methanol extracts on the TLC plate sprayed with Fe³⁺-2,4,6-Tri-2-pyridyl-s-triazine (TPTZ) showed that the compounds present in the extracts react differently to ferric ion, with most compounds unable to reduce ferric ion. Furthermore the methanol extracts were able to exhibit reduction potentials vs. Ag/AgCl at low concentrations. The compounds in the extracts were shown to be phenolic acids and flavonoid glycosides.]]> Wed 12 May 2021 20:35:11 SAST ]]> Expression of heat shock proteins on the plasma membrane of cancer cells : a potential multi-chaperone complex that mediates migration https://vital.seals.ac.za/vital/access/manager/Repository/vital:4122 Wed 12 May 2021 20:31:39 SAST ]]> A step forward in defining Hsp90s as potential drug targets for human parasitic diseases https://vital.seals.ac.za/vital/access/manager/Repository/vital:4110 Wed 12 May 2021 20:25:26 SAST ]]> Biochemical characterisation of Pfj2, a Plasmodium falciparum heat shock protein 40 chaperone potentially involved in protein quality control in the endoplasmic reticulum https://vital.seals.ac.za/vital/access/manager/Repository/vital:3883 Wed 12 May 2021 20:23:57 SAST ]]> Ectomycorrhizal characterisation, species diversity and community dynamics in Pinus patula Schelcht. et Cham. plantations https://vital.seals.ac.za/vital/access/manager/Repository/vital:3951 Wed 12 May 2021 20:17:22 SAST ]]> Enzymes with biocatalytic potential from Sorghum bicolor https://vital.seals.ac.za/vital/access/manager/Repository/vital:3908 Wed 12 May 2021 19:53:06 SAST ]]> Antimicrobial resistance patterns in a Port Elizabeth hospital https://vital.seals.ac.za/vital/access/manager/Repository/vital:4043 Wed 12 May 2021 19:40:59 SAST ]]> A molecular genetic assessment of the population structure and variation in two inshore dolphin genera on the east coast of South Africa https://vital.seals.ac.za/vital/access/manager/Repository/vital:4007 Wed 12 May 2021 19:29:13 SAST ]]> Binding and transcriptional activation by Uga3p, a zinc binuclear cluster protein of Saccharomyces cerevisiae redefining the UAS [subscript GABA] and the Uga3p binding site https://vital.seals.ac.za/vital/access/manager/Repository/vital:3933 Wed 12 May 2021 19:16:50 SAST ]]> Enzymatic recovery of rhodium(III) from aqueous solution and industrial effluent using sulphate reducing bacteria: role of a hydrogenase enzyme https://vital.seals.ac.za/vital/access/manager/Repository/vital:3956 Wed 12 May 2021 19:06:36 SAST ]]> A role for heat shock protein 90 (Hsp90) in fibronectin matrix dynamics https://vital.seals.ac.za/vital/access/manager/Repository/vital:4157 Wed 12 May 2021 18:59:18 SAST ]]> Biochemical mechanisms towards understanding Alzheimer's disease https://vital.seals.ac.za/vital/access/manager/Repository/vital:4103 Wed 12 May 2021 18:47:03 SAST ]]> Development of a hydantoin-hydrolysing biocatalyst for the production of optically pure amino acids using Agrobacterium tumefaciens strain RU-ORPN1 https://vital.seals.ac.za/vital/access/manager/Repository/vital:3943 Wed 12 May 2021 18:23:35 SAST ]]> BODIPY dyes for application in the photo-oxidation of pollutants, photodynamic antimicrobial chemotherapy, and nonlinear optics https://vital.seals.ac.za/vital/access/manager/Repository/vital:37859 Wed 12 May 2021 18:21:20 SAST ]]> Application of catalysts and nanomaterials in the design of an electrochemical sensor for ochratoxin A https://vital.seals.ac.za/vital/access/manager/Repository/vital:4121 Wed 12 May 2021 18:17:29 SAST ]]> Enhancing the saccharolytic phase of sugar beet pulp via hemicellulase synergy https://vital.seals.ac.za/vital/access/manager/Repository/vital:3955 Wed 12 May 2021 18:14:36 SAST ]]> Bioprocess development for removal of nitrogenous compounds from precious metal refinery wastewater https://vital.seals.ac.za/vital/access/manager/Repository/vital:4076 10,000 mg/I), numerous metals and high concentrations of those metals (> 20 mg/l of platinum group metals) in the wastewater are the main challenges for biological removal of nitrogenous compounds from PMR wastewater. Nitrogenous compounds such as NH₄⁺-N and N0₃-N are strong metal ligands, which make it difficult to recover metals from the wastewater. Therefore, a bioprocess was developed for removal of nitrogenous compounds from carefully simulated PMR wastewater. A preliminary investigation of metal wastewater was carried out to determine its composition and physico-chemical properties, the ability to nitrify and denitrify under different pH conditions and denitrification with different carbon Source compounds and amounts. Even at pH 4, nitrification could be carried out. A suitable hydraulic retention time was found to be 72 hours. There was no significant difference between sodium acetate and sodium lactate as carbon sources for denitrification. Based on these results, a reactor comparison study was carried out using simulated PMR wastewater in three types of reactors: continuously stirred tank reactor (CSTR), packed-bed reactor (PBR) and airlift suspension reactor (ALSR). These reactors were fed with 30 mg/l of Rh bound in an NH₄⁺ based compound (Claus salt: pentaaminechlororhodium (III) dichloride). Total nitrogen removal efficiencies of > 68 % , > 79 % and > 45 % were obtained in the CSTR, PBR and ALSR, respectively. Serially connected CSTR-PBR and PBR-CSTR reactor configurations were then studied to determine the best configuration for maximum removal of nitrogenous compounds from the wastewater. The PBR-CSTR configuration gave consistent biomass retention and automatic pH control in the CSTR. Ammonium removal efficiencies > 95 % were achieved in both reactors. As poor nitrate removal was observed a toxicity study was carried out using respirometry and the half saturation inhibition coefficients for Pt, Pd, Rh and Ru were found to be 15.81, 25.00, 33.34 and 39.25 mg/l, respectively. A mathematical model was developed to describe the nitrogen removal in PMR wastewater using activated sludge model number 1 (ASMl), two step nitrification and metal toxicity. An operational protocol was developed based on the literature review, experimental work and simulation results. The optimum reactor configuration under the set conditions (20 mg/I of Rh and < 100 mg/I of NH₄⁺-N) was found to be PBR-CSTR-PBR process, which achieved overall NH₄⁺-N and N0₃⁻-N removal efficiencies of > 90 % and 95 %, respectively. Finally, a rudimentary microbial characterisation was carried out on subsamples from the CSTR and PBRsecondary. It was found that the CSTR biomass consisted of both rods and cocci while PBRsecondary consisted of rods only. Based on these experimental works, further research needs and recommendations were made for optimisation of the developed bioprocess for removal of nitrogenous compounds from PMR wastewater.]]> Wed 12 May 2021 18:01:58 SAST ]]> Fungal remediation of winery and distillery wastewaters using Trametes pubescens MB 89 and the enhanced production of a high-value enzyme therein https://vital.seals.ac.za/vital/access/manager/Repository/vital:3932 Wed 12 May 2021 17:27:51 SAST ]]> Development of integrated biological processing for the biodesalination of sulphate- and metal-rich wastewaters https://vital.seals.ac.za/vital/access/manager/Repository/vital:3899 Wed 12 May 2021 17:09:38 SAST ]]> Biochemical characterization of plasmodium falciparum heat shock protein 70 https://vital.seals.ac.za/vital/access/manager/Repository/vital:4134 Wed 12 May 2021 17:09:04 SAST ]]> Bacterial degradation of the acaricide amitraz https://vital.seals.ac.za/vital/access/manager/Repository/vital:4099 Wed 12 May 2021 16:48:48 SAST ]]> Determination of distinctness among citrus cultivars using biochemical and molecular markers https://vital.seals.ac.za/vital/access/manager/Repository/vital:4022 Wed 12 May 2021 16:47:55 SAST ]]> Bacterial degradation of ixodicide amitraz https://vital.seals.ac.za/vital/access/manager/Repository/vital:4081 Wed 12 May 2021 16:44:06 SAST ]]> A study of the molecular variation between orbivirus proteins https://vital.seals.ac.za/vital/access/manager/Repository/vital:3892 Wed 12 May 2021 16:34:03 SAST ]]> Characterisation of Trypanosomal Type III and Type IV Hsp40 proteins https://vital.seals.ac.za/vital/access/manager/Repository/vital:3926 Wed 12 May 2021 16:16:44 SAST ]]> Development of experimental systems for studying the biology of Nudaurelia capensis ß virus https://vital.seals.ac.za/vital/access/manager/Repository/vital:3948 Wed 12 May 2021 16:14:46 SAST ]]> Development of an experimental system to investigate the interaction between the Helicoverpa armigera stunt virus capsid protein and viral RNA https://vital.seals.ac.za/vital/access/manager/Repository/vital:3946 Wed 12 May 2021 16:14:37 SAST ]]> An investigation of the role of mitochondrial STAT3 and modulation of Reactive Oxygen Species in adipocyte differentiation https://vital.seals.ac.za/vital/access/manager/Repository/vital:26595 Wed 12 May 2021 16:05:26 SAST ]]> An investigation into dopamine-melatonin interactions in the rat Corpus striatum and pineal gland: a possible pineal-striatal axis https://vital.seals.ac.za/vital/access/manager/Repository/vital:3906 Wed 12 May 2021 16:01:01 SAST ]]> Analysis of transcription factor binding specificity using ChIP-seq data. https://vital.seals.ac.za/vital/access/manager/Repository/vital:4115 Wed 12 May 2021 15:59:57 SAST ]]> Co-utilisation of microalgae for wastewater treatment and the production of animal feed supplements https://vital.seals.ac.za/vital/access/manager/Repository/vital:3940 90% of the algae population. Under batch operation the population dynamic shifted; Chlorella outcompeted Micractinium possibly due to nutrient depletion and selective grazing pressures caused by proliferation of Daphnia. Higher species diversity was observed during batch mode as slower growing algae were able to establish in the HRAP. Nutrient removal efficiency and biomass productivity was higher in continuous mode, however lower nutrient levels were obtained in batch operation. HMTBA did not significantly affect growth rate, however treatment with 10 mg.L-1 resulted in slightly increased growth rate in Micractinium and increased final biomass concentrations in Chlorella, Micractinium and Spirulina (although this was not statistically significant for Micractinium and Spirulina), which are known mixotrophic species. Algae treated with Cu-HMTBA, showed reduced final biomass concentration with 10 mg.L-1, caused by Cu toxicity. Biochemical composition of the algae was species-specific and differed through the growth cycle, with high protein observed during early growth and high carbohydrate during late growth/early stationary phase. Additionally, 0.1 mg.L-1 HMTBA and Cu-HMTBA significantly reduced protein content in Chlorella, Micractinium, Scenedesmus and Pediastrum. In conclusion, operation of the HRAP in continuous culture provided suitable wastewater treatment with high productivity of an ideal species, Micractinium, for use in animal feed supplementation. This species had 40% protein content during growth (higher than the other species tested) and dominated the HRAP at > 90% of the algae population during continuous mode. Addition of HMTBA (> 1 mg.L-1) to algae cultivation systems and those treating wastewater, has the potential to improve productivity and the value of the biomass by enhancing protein content. Overall, the co-utilisation of microalgae for wastewater treatment and the generation of a biomass rich in protein, for incorporation into formulated animal feed supplements, represents a closed ecosystem which conserves nutrients and regenerates a most valuable resource, water.]]> Wed 12 May 2021 15:55:36 SAST ]]> An investigation into cholinergic interactions in the rat pineal gland https://vital.seals.ac.za/vital/access/manager/Repository/vital:4048 Wed 12 May 2021 15:55:08 SAST ]]> Capsule immobilisation of sulphate-reducing bacteria and application in disarticulated systems https://vital.seals.ac.za/vital/access/manager/Repository/vital:3935 Wed 12 May 2021 15:49:47 SAST ]]> Analysis of bacterial Mur amide ligase enzymes for the identification of inhibitory compounds by in silico methods https://vital.seals.ac.za/vital/access/manager/Repository/vital:41036 Wed 12 May 2021 14:38:58 SAST ]]> Development and characterisation of a membrane gradostat bioreactor for the bioremediation of aromatic pollutants using white rot fungi https://vital.seals.ac.za/vital/access/manager/Repository/vital:4032 Wed 05 Apr 2023 07:00:15 SAST ]]> Ericoid mycorrhizal fungi and potential for inoculation of commercial berry species (Vaccinium corymbosium L.) https://vital.seals.ac.za/vital/access/manager/Repository/vital:4136 Thu 13 May 2021 10:28:15 SAST ]]> Characterization of the hydantoin-hydrolysing system of Pseudomonas putida RU-KM3s https://vital.seals.ac.za/vital/access/manager/Repository/vital:3939 Thu 13 May 2021 08:52:34 SAST ]]> Development of a novel, quantitative assay for determining the rate of activity of antimalarial drugs https://vital.seals.ac.za/vital/access/manager/Repository/vital:3884 Thu 13 May 2021 08:52:00 SAST ]]> Functional characterization of the nuclear localisation and export signals of the human Hsp70/Hsp90 organising protein (HOP) https://vital.seals.ac.za/vital/access/manager/Repository/vital:31489 Thu 13 May 2021 08:49:59 SAST ]]> Characterisation of the genome of Nudaurelia Omega Virus https://vital.seals.ac.za/vital/access/manager/Repository/vital:4023 Thu 13 May 2021 08:13:31 SAST ]]> An investigation into the antioxidative potential and regulatory aspects of liver tryptophan 2,3-dioxygenase by tryptophan and related analogues https://vital.seals.ac.za/vital/access/manager/Repository/vital:4010 Thu 13 May 2021 07:34:45 SAST ]]> A novel adjuvant : polymerised serum albumin beads https://vital.seals.ac.za/vital/access/manager/Repository/vital:4104 Thu 13 May 2021 07:27:26 SAST ]]> African mead biotechnology and indigenous knowledge systems in iQhilika process development https://vital.seals.ac.za/vital/access/manager/Repository/vital:3929 Thu 13 May 2021 07:14:41 SAST ]]> Biological sulphide oxidation in heterotrophic environments https://vital.seals.ac.za/vital/access/manager/Repository/vital:3919 Thu 13 May 2021 07:05:18 SAST ]]> Generation of polyclonal antibodies against Theiler's Murine Encephalomyelitis virus protein 2C, and their use in investigating localisation of the protein in infected cells https://vital.seals.ac.za/vital/access/manager/Repository/vital:3959 Thu 13 May 2021 07:01:49 SAST ]]> Cleaning of fouled membranes using enzymes from a sulphidogenic bioreactor https://vital.seals.ac.za/vital/access/manager/Repository/vital:4133 Thu 13 May 2021 06:54:33 SAST ]]> Bioaccumulation of metal cations by yeast and yeast cell components https://vital.seals.ac.za/vital/access/manager/Repository/vital:4046 Thu 13 May 2021 06:51:04 SAST ]]> Fundamental investigations into the factors affecting the response of laccase-based electrochemical biosensors https://vital.seals.ac.za/vital/access/manager/Repository/vital:4073 Thu 13 May 2021 06:37:23 SAST ]]> An investigation into the synergistic association between the major Clostridium cellulovorans cellulosomal endoglucanase and two hemicellulases on plant cell wall degradation https://vital.seals.ac.za/vital/access/manager/Repository/vital:3968 Thu 13 May 2021 06:31:22 SAST ]]> Development of integrated algal ponding systems in the treatment of wine distillery wastewaters https://vital.seals.ac.za/vital/access/manager/Repository/vital:4062 Thu 13 May 2021 06:26:33 SAST ]]> Fungal and substrate-associated factors affecting lignocellulolytic mushroom cultivation on wood sources available in South African [i.e. Africa] https://vital.seals.ac.za/vital/access/manager/Repository/vital:4020 Thu 13 May 2021 06:21:51 SAST ]]> A polarimetric method for collagenase activity measurement https://vital.seals.ac.za/vital/access/manager/Repository/vital:4052 Thu 13 May 2021 06:17:48 SAST ]]> Characterisation of the plasmodium falciparum Hsp40 chaperones and their partnerships with Hsp70 https://vital.seals.ac.za/vital/access/manager/Repository/vital:3938 Thu 13 May 2021 06:15:11 SAST ]]> Development of a novel in situ CPRG-based biosensor and bioprobe for monitoring coliform β-D-Galactosidase in water polluted by faecal matter https://vital.seals.ac.za/vital/access/manager/Repository/vital:3944 Thu 13 May 2021 06:01:30 SAST ]]> Floating sulphur biofilms structure, function and biotechnology https://vital.seals.ac.za/vital/access/manager/Repository/vital:3958 Thu 13 May 2021 05:51:33 SAST ]]> Falcipains as malarial drug targets https://vital.seals.ac.za/vital/access/manager/Repository/vital:3897 Thu 13 May 2021 05:43:16 SAST ]]> An investigation into the interaction partners of the scaffold protein human CNK1 in the NF-κB pathway https://vital.seals.ac.za/vital/access/manager/Repository/vital:31228 Thu 13 May 2021 05:39:44 SAST ]]> Evaluation and application of electroanalysis for the determination of antioxidants https://vital.seals.ac.za/vital/access/manager/Repository/vital:3922 Thu 13 May 2021 05:34:41 SAST ]]> Evaluation of a 'defouling on demand' strategy for the ultrafiltration of brown water using activatable enzymes https://vital.seals.ac.za/vital/access/manager/Repository/vital:3904 Thu 13 May 2021 05:05:44 SAST ]]> Biosulphidogenic hydrolysis of lignin and lignin model compounds https://vital.seals.ac.za/vital/access/manager/Repository/vital:3917 Thu 13 May 2021 05:04:53 SAST ]]> Establishing experimental systems for studying the replication biology of Providence virus https://vital.seals.ac.za/vital/access/manager/Repository/vital:3928 Thu 13 May 2021 05:03:04 SAST ]]> Characterization and mode of action of a bacteriocin produced by a Bacteroides Fragilis strain https://vital.seals.ac.za/vital/access/manager/Repository/vital:4124 Thu 13 May 2021 05:02:48 SAST ]]> Effect of alkaline pre-treatments on the synergistic enzymatic hydrolysis of sugarcane (Saccharum officinarum) bagasse by Clostridium cellulovorans XynA, ManA and ArfA https://vital.seals.ac.za/vital/access/manager/Repository/vital:3952 Thu 13 May 2021 04:58:57 SAST ]]> Characterisation of a plasmodium falciparum type II Hsp40 chaperone exported to the cytosol of infected erythrocytes https://vital.seals.ac.za/vital/access/manager/Repository/vital:4128 Thu 13 May 2021 04:58:25 SAST ]]> An investigation of the isolation, characterisation and application of hydantoinases for the industrial production of amino acids https://vital.seals.ac.za/vital/access/manager/Repository/vital:3969 Thu 13 May 2021 04:40:19 SAST ]]> Characterization of amide bond hydrolysis in novel hydantoinase-producing bacteria https://vital.seals.ac.za/vital/access/manager/Repository/vital:3911 Thu 13 May 2021 04:33:30 SAST ]]> Bacterial interaction in hide biodeterioration with special reference to selected Clostridium species https://vital.seals.ac.za/vital/access/manager/Repository/vital:4041 Thu 13 May 2021 04:32:37 SAST ]]> A process for the detanning of chrome leather wastes utilising tannery effluents https://vital.seals.ac.za/vital/access/manager/Repository/vital:4029 Thu 13 May 2021 04:31:38 SAST ]]> Characterisation of Human Hsj1a : an HSP40 molecular chaperone similar to Malarial Pfj4 https://vital.seals.ac.za/vital/access/manager/Repository/vital:4083 Thu 13 May 2021 04:19:34 SAST ]]> Enzymology of activated sewage sludge during anaerobic treatment of wastewaters : identification, characterisation, isolation and partial purification of proteases https://vital.seals.ac.za/vital/access/manager/Repository/vital:4012 Thu 13 May 2021 03:57:39 SAST ]]> Cleavage of the precursor coat protein of black beetle virus strain w17 in rabbit reticulocyte lysate https://vital.seals.ac.za/vital/access/manager/Repository/vital:3880 Thu 13 May 2021 03:40:51 SAST ]]> Elucidation and manipulation of the Hydantoin-Hydrolysing Enzyme System of Agrobacterium tumefaciens RU-OR for the Biocatalytic production of D-amino acids https://vital.seals.ac.za/vital/access/manager/Repository/vital:3916 Thu 13 May 2021 03:16:52 SAST ]]> Analysis of the interaction of Hsp90 with the extracellular matrix protein fibronectin (FN) https://vital.seals.ac.za/vital/access/manager/Repository/vital:4170 Thu 13 May 2021 03:15:16 SAST ]]> Bioaccumulation of heavy metals by the yeast S. cerevisiae and the bioremediation of industrial waste water https://vital.seals.ac.za/vital/access/manager/Repository/vital:4015 chitin> glucan > intact cell walls exists. However, these components differ in their affinities for metal ions. Storage of metal ions within the cell occurs predominantly in the vacuole. The present study concluded that metal accumulation by the vacuole could be related to size. Metal accumulation occurred in the order of Cu2+ > Co2+ > Cd2+ with a corresponding decrease in atomic radii of Cd2+ > C02+ > Cu2+. Vacuolar ion deposition occurs at an early stage during the internalization of metal ions within the yeast cells. At the onset of vacuolar saturation, depositions of metal ions as granules within the cytosol occurs. In the presence of heavy metal cations viable yeast cells can be shown to exhibit two types of cellular responses. Uptake of Cu2+ and Cd2+ causes the loss of intracellular physiological cations from within the yeast cell. In comparison, uptake of Co2+ into the cell does not have this effect. All three heavy metal cations initiate plasma cell membrane permeability, thus the Cu2+ and Cd2+ induced loss of the intracellular cations, occurs. ~ a result of ion-exchange mechanisms and not due to cation leakage brought about by membrane permeabilization. Uptake of heavy metals by viable yeasts appears to be generally non-selective though the amount of metals accumulated are largely affected by the ratio of ambient metal concentration to biomass quantity. In addition, the energy dependent nature of internalization necessitates the availability of an external energy source for metal uptake by viable yeast cells. For these reasons metal removal from industrial waste water was investigated using non-viable biomass. By immobilizing the yeast cells additional mechanical integrity and stability was conferred apon the biomass. The three types of biomass preparations developed in this study, viz. polyvinyl alcohol (PV A) Na-alginate, PV A Na-orthophosphate and alkali treated polyethylenimine (PEI):glutaraldehyde (GA) biomass pellets, all fulfilled the necessary physical requirements. However, the superior metal accumulating properties of the PEI:GA biomass determined its selection as a biosorbent for bioremediation purposes. Biosorption of heavy metals by PEI:GA biomass is of a competitive nature, with the amount of metal accumulated influenced by the availability of the metal ions. This availability is largely determined by the solution pH. At low pH values the affinity of the biomass for metals decreases, whilst enhanced metal biosorption occurs at higher pHs, ego pH 4.5 - 6.0. PEI:GA biomass pellets can be implemented -as a biosorbent for the bi9remediaiton of high concentration, low-volume metal containing industrial waste. Several options regarding the bioremediation system are available. Depending on the concentration of the metals in the effluent, the bioremediation process can either be used independently or as part of a biphasic remediation system for the treatment of waste water. Initial phase chemical modification may be required, whilst two types of biological systems can be implemented as 'part of the second phase. The PEI:GA biomass can either be contained within continuous-flow fixed bed tanks or continuous-flow stirred bioreactor tanks. Due to the simplicity of the process and the ease with which scale-up is facilitated, the second type of system shows greater application potential for the treatment of this type of industrial waste water than the fixed-bed systems.]]> Thu 13 May 2021 02:58:09 SAST ]]> Accelerated carbon dioxide deliming of cattle hides and sheepskins https://vital.seals.ac.za/vital/access/manager/Repository/vital:3918 Thu 13 May 2021 02:17:58 SAST ]]> Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70 https://vital.seals.ac.za/vital/access/manager/Repository/vital:4117 Thu 13 May 2021 02:12:44 SAST ]]> An investigation into the replication biology of Helicoverpa armigera stunt virus https://vital.seals.ac.za/vital/access/manager/Repository/vital:3967 Thu 13 May 2021 02:10:17 SAST ]]> Epidemiological and aetiological aspects of diarrhoeal disease in the Eastern Cape https://vital.seals.ac.za/vital/access/manager/Repository/vital:4045 Thu 13 May 2021 02:07:26 SAST ]]> A central enrichment-based comparison of two alternative methods of generating transcription factor binding motifs from protein binding microarray data https://vital.seals.ac.za/vital/access/manager/Repository/vital:3890 Thu 13 May 2021 01:56:09 SAST ]]> An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites https://vital.seals.ac.za/vital/access/manager/Repository/vital:4109 Thu 13 May 2021 01:52:04 SAST ]]> Assembly of Omegatetravirus virus-like particles in the yeast Saccharomyces cerevisiae https://vital.seals.ac.za/vital/access/manager/Repository/vital:3930 Thu 13 May 2021 01:44:19 SAST ]]> Characterisation of the J domain aminoacid residues important for the interaction of DNAJ-like proteins with HSP70 chaperones https://vital.seals.ac.za/vital/access/manager/Repository/vital:3937 Thu 13 May 2021 01:19:45 SAST ]]> An investigation into the neuroprotective properties of melatonin https://vital.seals.ac.za/vital/access/manager/Repository/vital:3900 Thu 13 May 2021 01:07:11 SAST ]]> A study of carbonate-rich brines from Sua Pan to characterize organic contaminants in the soda ash process https://vital.seals.ac.za/vital/access/manager/Repository/vital:4031 Thu 13 May 2021 01:00:06 SAST ]]> Bacterial degradation of waste coal https://vital.seals.ac.za/vital/access/manager/Repository/vital:26590 Thu 13 May 2021 00:39:44 SAST ]]> A baculovirus-mediated expression system for the analysis of HaSV RNA packaging https://vital.seals.ac.za/vital/access/manager/Repository/vital:4025 Thu 13 May 2021 00:34:02 SAST ]]> An investigation into the effects of inorganic toxins and tryptophan metabolites on the forebrain cholinergic system and the pineal gland of the rat https://vital.seals.ac.za/vital/access/manager/Repository/vital:4018 Thu 13 May 2021 00:24:29 SAST ]]> A lignocellulolytic enzyme system for fruit waste degradation : commercial enzyme mixture synergy and bioreactor design https://vital.seals.ac.za/vital/access/manager/Repository/vital:4114 Thu 13 May 2021 00:22:21 SAST ]]> A comparative bioinformatic analysis of zinc binuclear cluster proteins https://vital.seals.ac.za/vital/access/manager/Repository/vital:4004 Thu 13 May 2021 00:20:34 SAST ]]> Characterisation of the cellulolytic and hemicellulolytic system of Bacillus Licheniformis SVD1 and the isolation and characterisation of a multi-enzyme complex https://vital.seals.ac.za/vital/access/manager/Repository/vital:3936 Thu 13 May 2021 00:16:00 SAST ]]> An investigation into the biological treatment of platinum refinery effluent https://vital.seals.ac.za/vital/access/manager/Repository/vital:45334 Fri 19 Nov 2021 09:15:59 SAST ]]> An investigation into the biological treatment of platinum refinery effluent using the plant Azolla Filiculoides https://vital.seals.ac.za/vital/access/manager/Repository/vital:45333 Fri 19 Nov 2021 08:33:53 SAST ]]> Biocatalytic and biomimetic studies of polyphenol oxidase https://vital.seals.ac.za/vital/access/manager/Repository/vital:4028 Fri 06 Aug 2021 10:23:20 SAST ]]>