O Brasil é o maior produtor mundial de cana-de-açúcar, sendo o Estado de São Paulo responsável por mais de 50% do total desta produção. Esta cultura tem um enorme impacto sobre a agricultura brasileira e devido a isto, uma melhor compreensão da composição da comunidade microbiana relacionada a ciclagem do nitrogênio (N) nestes solos é de grande importância para o aprimoramento no cultivo da cana-de-açúcar. No entanto, pouco se sabe sobre a relação entre grupos microbianos e essa cultura. Este trabalho visou determinar variações nas comunidades microbianas que participam das transformações do N nos solos de três áreas utilizadas para a produção de cana-de-açúcar (A, F e J), as quais apresentam uma gama de diferentes condições de manejo e características do solo. Cada área foi analisada em triplicatas, e o DNA extraído do solo foi utilizado para metodologias de sequenciamento de segunda geração (metagenômica e sequenciamento do gene 16S rDNA), PCR quantitativo (qPCR) e polimorfismo dos fragmentos terminais de restrição (T-RFLP). A maioria das sequências derivaram de bactérias (98%; base de dados M5NR); seis etapas do ciclo do nitrogênio foram anotadas pela plataforma MG-RAST (base de dados SEED): amonificação do nitrato e nitrito (ANN); fixação de nitrogênio; desnitrificação; óxido nítrico sintase; redução dissimilatória do nitrito e assimilação de amônia. Este último passo mencionado foi o mais abundante (28%) (genes gltb e gltD) e está diretamente relacionado a multiplicação microbiana nos solos.. O segundo processo mais abundante foi ANN (genes nir e nar), responsável por consumir este substrato durante o ciclo. Proteobacteria, Chloroflexi, Verrucomicrobia e Cyanobacteria estão presentes em todas as etapas do ciclo, representando microrganismos que podem participar das vias de transformação do N e, ademais, foi possível descrever um core microbiano (nível de ordem) representado por Sphingomonadales. Algumas variáveis ambientais, como a aplicação de torta de filtro e a produtividade mostraram uma correlação significativa com a estrutura da comunidade microbiana. Isto também foi encontrado para algumas características do solo como fósforo, magnésio e matéria orgânica. Além disso, identificou-se uma alta abundância de microrganismos carregando genes que codificam enzimas da via de redução do nitrato e nitrito. Portanto, apesar de sua complexidade, o estudo das funções microbianas de nitrogênio em solos cultivados com cana-de-açúcar é inovador por acessar de forma conjunta todas as comunidades envolvidas neste ciclo, caracterizadas por sequenciamento, o que evita os problemas inerentes ao cultivo microbiano, além de permitir inferir sobre a hierarquia das variáveis ambientais que influem sobre esse grupos microbianos. / Brazil is the largest world\'s producer of sugarcane and State of São Paulo accounts for over 50% of this production. This crop has a huge impact on Brazilian agriculture and due to this great importance, a better understanding of the composition of the microbial community related to cycling of nitrogen (N) in these soils is of utmost importance for the improvement in the cultivation of sugarcane. However, little is known about the relationship between microbial groups and this crop. This study aimed to determine changes in microbial communities that participate in the transformation of N in soils derived from three areas used for sugarcane production (named A, F and J), which have a range of different management conditions and soil characteristics. Each area was analyzed in triplicate, and the extracted DNA was used to develop next generation sequencing (shotgun metagenomics and 16S rDNA), quantitative PCR (qPCR) and terminal restriction fragment length polymorphism (T-RFLP). Most of the sequences derived from Bacteria (98%; M5NR database); six stages of nitrogen cycle were annotated by MG-RAST plataform (SEED database): nitrate and nitrite ammonification (NNA); nitrogen fixation; denitrification; nitric oxide synthase; dissimilatory nitrite reductase and ammonia assimilation. This last mentioned step was the most abundant (28%) (gltB and gltD genes) and is directly linked to microbial growth in soil, since the final product of the reaction is glutamate. The second most abundant process was NNA (nir and nar genes), responsible for consuming this substrate during the cycle. Proteobacteria and Chroloflexi are present at all stages of the cycle, representing microorganisms that can participate in the N transformation and, moreover, it was possible to describe a microbial core (at an order level) represented by Sphingomonadales. Some environmental variables, such as the application of filter cake and productivity showed a significant correlation with the structure of the microbial community. This was also found for certain soil characteristics such as phosphorus, magnesium and organic matter. In addition, it was identified a high abundance of microorganisms carrying genes encoding the enzymes for nitrate and nitrite reduction pathway. Therefore, despite its complexity, the study of microbial functions of nitrogen in soils cultivated with sugarcane is innovative by accessing jointly all communities involved in this cycle, characterized by sequencing, which avoids the problems inherent in microbial cultivation and allows to infer about the hierarchy of environmental variables that influence this microbial groups.

Estudos sobre a diversidade de Bacteria em solos de mangue (Brasil) e marisma (Espanha) são escassos. A vegetação de mangue, composta por espécies como Spartina alterniflora, Rhizophora mangle, Avicennia schaueriana e Laguncularia racemosa, pode ser um dos fatores que determinam a estruturação das comunidades de procariotos. Determinações das estruturas das comunidades e de diversidade de Bacteria podem ocorrer em função das diferentes condições físico-químicas dos solos, refletindo na configuração dos processos biogeoquímicos. O objetivo deste trabalho foi avaliar a variação das estruturas das comunidades de Bacteria e Archaea, bem como a diversidade, em solos de mangue e marisma utilizando DGGE e sequenciamento parcial do rDNA 16S. As estruturas das comunidades de procariotos apresentaram variações em função de condições de vegetação. Proteobacteria e Bacteroidetes estão presentes em todos os solos estudados. A comunidade de Bacteria destes ambientes é dominada por Proteobacteria. Vários dos táxons detectados estão relacionados com ciclos biogeoquímicos importantes para os ambientes estudados. As estimativas não-paramétricas de riqueza de espécies (ACE e Chao1) mostram que solos de mangue e marisma podem conter milhares de espécies de bactérias. As comunidades de Bacteria dos solos de mangue e marisma são significativamene diferentes. Na camada mais superficial do sedimento de mangue predomina Euryarchaeota metanogênicas enquanto que na camada mais profunda predomina Crenarchaeota. Bactérias das ordens Desulfobacterales, Desulfovibrionales e Desulfuromonales podem estar relacionadas com a atividade de sulfato-redução e formação de pirita na camada anaeróbia do perfil de solo de marisma. De uma maneira geral, pode-se concluir que a diversidade e estrutura das comunidades de procariotos de ambientes estuarinos pode variar em função da vegetação estabelecida e do tipo de ambiente. Adicionalmente, solos de mangue e marisma possuem grande diversidade de procariotos, grande parte da qual é desconhecida, podendo representar elevado potencial genético para utilização biotecnológica. / The bacterial diversity in mangrove (Brazil) and marisma (Espanha) soils are largely unknown. Bacterial communities participate in biogeochemicals processes that occurs in soils of estuarine ecosystems. Determinations of the bacterial communities structures and diversity can occur in function of different physico-chemical conditions, reflecting in the biogeochemical processes. The aim of this work was to evaluate the variation of bacterial an archaeal communities structures utilizing DGGE and partial sequencing of 16S rDNA. Bacterial community structures showed more similarity between repetitions samples than the areas under different vegetation. Phylogenetic afiliation shows that several sequences were not clamped into known phyla. Proteobacteria prevails in bacterial communities of mangrove and marisma soils. Several taxa detected are associated to important biogeochemical cycles that occur in estuarine ecosystems. Analysis of species richness showed that mangrove and marisma soils can contain 200 to 6000 species of bacteria. Methanogenic Euryarchaeota was found specially in the upper sample of mangrove sediment analysed whereas the Crenarchaeota was found specially in the lower. Based on the data obtained, it can be concluded that the vegetation is one of the factors affecting the structure of bacterial and archaeal communities in mangrove soils. Additionaly, the effects of edafic factors and seasonal variations have to be considered as determining the prokaryotic community sctuctures, and bacterial and archaeal communities can respond independently to the factors that determine their community structures. Bacterial diversity can vary with the studied estuarine ecosystem. Studies are necessary concerning to diversity of Bacteria, it variation and correlation with biogeochemical process in the mangrove and marisma soils. These soils show a great diversity of bacteria, much of than unknown, which represent a great genetic potential to the biotechnology.

O Brasil é o maior produtor mundial de cana-de-açúcar, sendo o Estado de São Paulo responsável por mais de 50% do total desta produção. Esta cultura tem um enorme impacto sobre a agricultura brasileira e devido a isto, uma melhor compreensão da composição da comunidade microbiana relacionada a ciclagem do nitrogênio (N) nestes solos é de grande importância para o aprimoramento no cultivo da cana-de-açúcar. No entanto, pouco se sabe sobre a relação entre grupos microbianos e essa cultura. Este trabalho visou determinar variações nas comunidades microbianas que participam das transformações do N nos solos de três áreas utilizadas para a produção de cana-de-açúcar (A, F e J), as quais apresentam uma gama de diferentes condições de manejo e características do solo. Cada área foi analisada em triplicatas, e o DNA extraído do solo foi utilizado para metodologias de sequenciamento de segunda geração (metagenômica e sequenciamento do gene 16S rDNA), PCR quantitativo (qPCR) e polimorfismo dos fragmentos terminais de restrição (T-RFLP). A maioria das sequências derivaram de bactérias (98%; base de dados M5NR); seis etapas do ciclo do nitrogênio foram anotadas pela plataforma MG-RAST (base de dados SEED): amonificação do nitrato e nitrito (ANN); fixação de nitrogênio; desnitrificação; óxido nítrico sintase; redução dissimilatória do nitrito e assimilação de amônia. Este último passo mencionado foi o mais abundante (28%) (genes gltb e gltD) e está diretamente relacionado a multiplicação microbiana nos solos.. O segundo processo mais abundante foi ANN (genes nir e nar), responsável por consumir este substrato durante o ciclo. Proteobacteria, Chloroflexi, Verrucomicrobia e Cyanobacteria estão presentes em todas as etapas do ciclo, representando microrganismos que podem participar das vias de transformação do N e, ademais, foi possível descrever um core microbiano (nível de ordem) representado por Sphingomonadales. Algumas variáveis ambientais, como a aplicação de torta de filtro e a produtividade mostraram uma correlação significativa com a estrutura da comunidade microbiana. Isto também foi encontrado para algumas características do solo como fósforo, magnésio e matéria orgânica. Além disso, identificou-se uma alta abundância de microrganismos carregando genes que codificam enzimas da via de redução do nitrato e nitrito. Portanto, apesar de sua complexidade, o estudo das funções microbianas de nitrogênio em solos cultivados com cana-de-açúcar é inovador por acessar de forma conjunta todas as comunidades envolvidas neste ciclo, caracterizadas por sequenciamento, o que evita os problemas inerentes ao cultivo microbiano, além de permitir inferir sobre a hierarquia das variáveis ambientais que influem sobre esse grupos microbianos. / Brazil is the largest world\'s producer of sugarcane and State of São Paulo accounts for over 50% of this production. This crop has a huge impact on Brazilian agriculture and due to this great importance, a better understanding of the composition of the microbial community related to cycling of nitrogen (N) in these soils is of utmost importance for the improvement in the cultivation of sugarcane. However, little is known about the relationship between microbial groups and this crop. This study aimed to determine changes in microbial communities that participate in the transformation of N in soils derived from three areas used for sugarcane production (named A, F and J), which have a range of different management conditions and soil characteristics. Each area was analyzed in triplicate, and the extracted DNA was used to develop next generation sequencing (shotgun metagenomics and 16S rDNA), quantitative PCR (qPCR) and terminal restriction fragment length polymorphism (T-RFLP). Most of the sequences derived from Bacteria (98%; M5NR database); six stages of nitrogen cycle were annotated by MG-RAST plataform (SEED database): nitrate and nitrite ammonification (NNA); nitrogen fixation; denitrification; nitric oxide synthase; dissimilatory nitrite reductase and ammonia assimilation. This last mentioned step was the most abundant (28%) (gltB and gltD genes) and is directly linked to microbial growth in soil, since the final product of the reaction is glutamate. The second most abundant process was NNA (nir and nar genes), responsible for consuming this substrate during the cycle. Proteobacteria and Chroloflexi are present at all stages of the cycle, representing microorganisms that can participate in the N transformation and, moreover, it was possible to describe a microbial core (at an order level) represented by Sphingomonadales. Some environmental variables, such as the application of filter cake and productivity showed a significant correlation with the structure of the microbial community. This was also found for certain soil characteristics such as phosphorus, magnesium and organic matter. In addition, it was identified a high abundance of microorganisms carrying genes encoding the enzymes for nitrate and nitrite reduction pathway. Therefore, despite its complexity, the study of microbial functions of nitrogen in soils cultivated with sugarcane is innovative by accessing jointly all communities involved in this cycle, characterized by sequencing, which avoids the problems inherent in microbial cultivation and allows to infer about the hierarchy of environmental variables that influence this microbial groups.

At the commencement of this study, some sensitive overseas markets were rejecting chilled vacuum-packed New Zealand lamb due to higher than expected total viable counts, and counts of Enterobacteriaceae, a family of bacteria used to indicate sanitary condition. Of the many factors that influence the bacterial composition of chilled lamb in the overseas marketplace, the meat producer can only exert significant control over: Hygiene, ensuring the bacterial viable count on the meat prior to packaging is as low as possible, and comprised of as few species as possible that are capable of anaerobic growth at chilled meat temperatures. Maintaining the pH of the meat within acceptable limits, by careful animal selection and minimal pre-slaughter stress. Refrigeration temperatures, through rigorous maintenance of the cold-chain. The type of preservative packaging used, which is often limited by regulation in the marketplace. Initial work established that the bacterial microbiota present on the meat contact surfaces in the butchering facilities at some premises, in particular conveyor belting, was excessive and comprised of species that contributed to the high counts on the meat reported above. As a means of improving the hygiene of this process, this study investigated the hypothesis that some species of bacteria were able to form biofilms on the conveyor belt contact surfaces, becoming reservoirs for cross-contamination. This hypothesis was not been proven by this work; the results showing that biofilms were not present and that adequate hygiene of these surfaces instead depends on the ability to remove all meat-based residues from them at the completion of each day's processing. For premises operating interlocking belts from one manufacturer (Intraloxreg), a clean-in-place system is now available that is able to achieve this. Premises operating conventional disinfectant and water sanitisation of either continuous or interlocking belts must ensure that meat residue is completely removed before disinfection. The majority of New Zealand meat industry premises can now demonstrate that their hygienic processes in this area are under control. The microbiota of conveyor belting in this study was found to consist of bacteria from five taxonomic groups; the Flavobacteriaceae, the Actinomycetales, the Bacillus/Clostridium group, and the alpha and gamma branches of the Proteobacteria. The genera present on belts from premises whose hygiene was found to be in control did not contain species known to cause food-borne disease or spoilage of vacuum packaged meats. The bacterial viable count remains the most effective method available at this time for monitoring conveyor belt hygiene. Attempts to develop a monitoring system based on microscopy of an in-situ sampling device were unsuccessful due to an inability to penetrate the meat residue matrix. Denaturing Gradient Gel Electrophoresis (DGGE) may offer an alternative for rapid investigation of diversity, but further work is required before this can be validated for routine use.

Bacteria play important roles in the transformation of nutrients in wetlands, but few studies have examined parameters affecting variation in bacterial community composition between wetlands. We compared the composition of eubacterial and denitrifying bacterial biofilm communities in 32 agricultural constructed wetlands in southern Sweden, and the extent to which wetland environmental parameters could explain the observed variation. Structure and richness of the eubacterial 16S rRNA gene and three denitrifying bacterial enzyme genes (nirK, nirS and nosZ), analysed by molecular fingerprinting methods, varied among the constructed wetlands, which could be partly explained by different environmental parameters. Results from the enzyme gene analyses were also compared to determine whether the practice of using a single denitrifying bacterial gene could characterize the overall community composition of denitrifying bacteria. We found that nirK was more diverse than both nirS and the nosZ, and the band structure and richness of the three genes were not related to the sam environmental parameters. This suggests that using a single enzyme gene may not suffice to characterize the community composition of denitrifying bacteria in constructed agricultural wetlands. / <p>Included in doctoral thesis: Milenkovski, Susann. Structure and Function of Microbial Communities in Constructed Wetlands - Influence of environmental parameters and pesticides on denitrifying bacteria. Lund University 2009.</p>

Phytopathogenic bacterium, Xylella fastidiosa, causes a number of economically important diseases, including Pierces disease (PD) of grape and bacterial leaf scorch (BLS) of a number of landscape trees. In Kentucky (KY), BLS affects a number of shade trees including many oak and maple species. In 2001, PD was diagnosed in grapevines in western KY. Xylella fastidiosa is also detected in many asymptomatic landscape plants and grasses. It was the goal of this research to identify hosts of X. fastidiosa around KY and use phylogenetic analysis to compare sequences of the 16S rDNA and gyrase B (gyrB) genes between samples. This research tests the hypothesis that sequence comparison can identify asymptomatic hosts and vectors that serve as a source of inoculum for pathogenic strains of X. fastidiosa. Plant collections were done in urban areas of KY between 2002 and 2004 and samples were tested for the presence of X. fastidiosa by ELISA and PCR. A number of symptomatic and asymptomatic plants were found to be hosts. Primer sets specifically developed for X. fastidiosa were used to amplify part of the 16S rDNA and the gyrB gene from DNA extracted directly from plant tissue. Sequence data from these specifically amplified products were assembled using Phrap, aligned with ClustalW, then phylogenetic analysis was done with Paup 4.0b10 beta. Comparisons with strains outside of Kentucky were also done using X. fastidiosa sequence obtained from NCBI. Maximum parsimony (MP) trees from the 16S rDNA showed a clade of sequence from oak and grass samples that is an outgroup to sequence from NCBI and other samples in this study. According to BLAST, sequences in this outgroup clade seem to be more closely related to the genera Xanthomonas or Stenotrophomonas than Xylella. However, the gyrB gene MP tree showed sequence from three of the samples that were part of this outgroup clade as being closely related to those X. fastidiosa sequences that are part of the ingroup of both 16S rDNA and gyrB trees. The topology difference between the 16S rDNA and gyrB trees suggest there may have been recombination in the genomic region containing one of these genes.

Contamination from various sources has a huge impact on soil health and microbial community composition. Metal contamination of soil in mining scenarios is of concern and is not adequately addressed, particularly with respect to the microbial community. The mining industry is one of the largest contributors to heavy metal contamination of soil in South Africa, especially since the country is one of the major mining countries in the world. Platinum mining is of special importance, since the largest percentage of the world’s reserves of platinum group metals are found and mined in South Africa. Metals from mining activities become irreversibly immobilized in soil systems because they cannot be degraded and has a huge impact on soil systems. In this study, bacteria was isolated from soil samples collected from a platinum mine tailings dam outside Rustenburg. During the warm sampling season (March 2006) most isolates were found, especially in sites 3 and 4. During the colder and drier season (May 2006) there were less isolates. Most of the isolated cultures also displayed a wide temperature growth range, mostly between 24°C - 37°C. Paenibacillus lautus and Bacillus subtilus DN-10 had a growth range between 5°C - 40°C. Culturable metal tolerant bacteria were isolated, purified and identified using 16S rDNA sequences. Nine different species were found namely Paenibacillus lautus strain DS19, Paenibacillus lautus, Paenibacillus sp. C15, uncultured Paenibacillaceae, Bacillus subtilis strain DN-10, Bacillus sp. KDNB5, Bacillus cereus, Stenotrophomonas maltophilia and Alcaligenes sp. DJWH 146-2. The ability of these strains to tolerate metal concentrations were explored by determining their minimum inhibitory concentrations for a selection of metals e.g. aluminum, barium, cobalt, chromium, cadmium, copper, iron, lead, manganese, nickel and mercury. Most isolates were able to tolerate >5mM of the Al\Ni alloy and cobalt. Transmission electron microscopy was used to determine the location of metals inside bacterial cells and electron dispersive X-ray analysis was used to determine the levels of metals inside microbial cells. Bacillus subtilis DN-10 (LDK0306) showed a high MIC (>5mM) for most metals used, except Hg. This strain also had a high percentage (10.26%) of Pb detected in its cells by EDX. This was the highest percentage detected. Plasmids were extracted from the identified strains and can help gain a better understanding of metal tolerance mechanisms used by these isolates. / Thesis(MSc (Environmental Sciences))--North-West University, Potchefstroom Campus, 2013

Contamination from various sources has a huge impact on soil health and microbial community composition. Metal contamination of soil in mining scenarios is of concern and is not adequately addressed, particularly with respect to the microbial community. The mining industry is one of the largest contributors to heavy metal contamination of soil in South Africa, especially since the country is one of the major mining countries in the world. Platinum mining is of special importance, since the largest percentage of the world’s reserves of platinum group metals are found and mined in South Africa. Metals from mining activities become irreversibly immobilized in soil systems because they cannot be degraded and has a huge impact on soil systems. In this study, bacteria was isolated from soil samples collected from a platinum mine tailings dam outside Rustenburg. During the warm sampling season (March 2006) most isolates were found, especially in sites 3 and 4. During the colder and drier season (May 2006) there were less isolates. Most of the isolated cultures also displayed a wide temperature growth range, mostly between 24°C - 37°C. Paenibacillus lautus and Bacillus subtilus DN-10 had a growth range between 5°C - 40°C. Culturable metal tolerant bacteria were isolated, purified and identified using 16S rDNA sequences. Nine different species were found namely Paenibacillus lautus strain DS19, Paenibacillus lautus, Paenibacillus sp. C15, uncultured Paenibacillaceae, Bacillus subtilis strain DN-10, Bacillus sp. KDNB5, Bacillus cereus, Stenotrophomonas maltophilia and Alcaligenes sp. DJWH 146-2. The ability of these strains to tolerate metal concentrations were explored by determining their minimum inhibitory concentrations for a selection of metals e.g. aluminum, barium, cobalt, chromium, cadmium, copper, iron, lead, manganese, nickel and mercury. Most isolates were able to tolerate >5mM of the Al\Ni alloy and cobalt. Transmission electron microscopy was used to determine the location of metals inside bacterial cells and electron dispersive X-ray analysis was used to determine the levels of metals inside microbial cells. Bacillus subtilis DN-10 (LDK0306) showed a high MIC (>5mM) for most metals used, except Hg. This strain also had a high percentage (10.26%) of Pb detected in its cells by EDX. This was the highest percentage detected. Plasmids were extracted from the identified strains and can help gain a better understanding of metal tolerance mechanisms used by these isolates. / Thesis(MSc (Environmental Sciences))--North-West University, Potchefstroom Campus, 2013

The aim of this study was to determine the effects of the heavy metal pollution on microbial diversity along the gradient from a platinum mine tailings dam using culture-dependent (plating methods) and molecular methods. Tailings and soil samples were collected from seven sites (6 samples per site) at increasing distances from the tailings dam. Samples were collected over a two year period and included two rainy and two dry periods. Concentrations of various heavy metals were determined using an inductively coupled plasma mass spectrometer (ICP-MS). The results demonstrated that seasonal variations in metal concentrations occurred and also that concentrations were significantly different'(P < 0.05) between the experimental sites for each metal. The relative relationship between metals was in the following order: Al > Ni > Cu > Cr. Since soil metal concentration benchmarks for South Africa are lacking, the concentrations were compared to the Canadian microbial benchmarks (MB) and Netherlands maximum permissible concentrations (MPC). Concentrations of most of the heavy metals exceeded the MB and MPC. Levels and diversity of culturable fungi and bacteria at each site were determined using plate count methods. Results indicated that levels of bacteria and fungi were not suppressed by high concentrations of heavy metals. Significantly higher levels (P < 0.05) of fungi were found at the sites on the tailings dam (higher concentrations of heavy metals), compared to sites more than 300 m away. A commonly used soil health index (Shannon-Weaver diversity index) was used to compare microbial community diversity at each site and to evaluate whether or not the heavy metal contamination impacted negatively on these soil bacterial and fungal communities. Shannon-Weaver diversity indices were higher at sites on and close to the tailings dam than sites more than 300 m away. However, ratio of fungal to bacterial levels as determined by plate counts was inconsistent. Representatives of bacterial species that were grouped using colony morphology and whole cell protein profiles were identified by 16S rDNA sequences as Bacillus barbaricus (B. barbaricus) and -Paenibacillus lautus {P. Lautus). Restriction enzyme digest, SDS-PAGE and random amplified polymorphic DNA (RAPD) analyses provided supporting evidence that representatives were correctly grouped. Cluster analysis results demonstrated that the RAPD profiles of the metal tolerant P. lautus representatives were sufficiently dissimilar to discriminate between individuals from the spatially separated sites. The spatially separated sites also represented sites with high and low heavy metal concentrations. Observed genetic variability was thus also associated with varying levels of heavy metals. In conclusion, this study demonstrated the potential of using RAPD analysis as biomarkers for genotoxic effects of heavy metals on bacterial genomes. / Masters / Thesis (M.Sc. (Microbiology))--North-West University, Potchefstroom Campus, 2009.

The aim of this study was to determine the effects of the heavy metal pollution on microbial diversity along the gradient from a platinum mine tailings dam using culture-dependent (plating methods) and molecular methods. Tailings and soil samples were collected from seven sites (6 samples per site) at increasing distances from the tailings dam. Samples were collected over a two year period and included two rainy and two dry periods. Concentrations of various heavy metals were determined using an inductively coupled plasma mass spectrometer (ICP-MS). The results demonstrated that seasonal variations in metal concentrations occurred and also that concentrations were significantly different'(P < 0.05) between the experimental sites for each metal. The relative relationship between metals was in the following order: Al > Ni > Cu > Cr. Since soil metal concentration benchmarks for South Africa are lacking, the concentrations were compared to the Canadian microbial benchmarks (MB) and Netherlands maximum permissible concentrations (MPC). Concentrations of most of the heavy metals exceeded the MB and MPC. Levels and diversity of culturable fungi and bacteria at each site were determined using plate count methods. Results indicated that levels of bacteria and fungi were not suppressed by high concentrations of heavy metals. Significantly higher levels (P < 0.05) of fungi were found at the sites on the tailings dam (higher concentrations of heavy metals), compared to sites more than 300 m away. A commonly used soil health index (Shannon-Weaver diversity index) was used to compare microbial community diversity at each site and to evaluate whether or not the heavy metal contamination impacted negatively on these soil bacterial and fungal communities. Shannon-Weaver diversity indices were higher at sites on and close to the tailings dam than sites more than 300 m away. However, ratio of fungal to bacterial levels as determined by plate counts was inconsistent. Representatives of bacterial species that were grouped using colony morphology and whole cell protein profiles were identified by 16S rDNA sequences as Bacillus barbaricus (B. barbaricus) and -Paenibacillus lautus {P. Lautus). Restriction enzyme digest, SDS-PAGE and random amplified polymorphic DNA (RAPD) analyses provided supporting evidence that representatives were correctly grouped. Cluster analysis results demonstrated that the RAPD profiles of the metal tolerant P. lautus representatives were sufficiently dissimilar to discriminate between individuals from the spatially separated sites. The spatially separated sites also represented sites with high and low heavy metal concentrations. Observed genetic variability was thus also associated with varying levels of heavy metals. In conclusion, this study demonstrated the potential of using RAPD analysis as biomarkers for genotoxic effects of heavy metals on bacterial genomes. / Masters / Thesis (M.Sc. (Microbiology))--North-West University, Potchefstroom Campus, 2009.