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Structural, functional and evolutionary studies on 6-oxopurine phosphoribosyltransferases (PRTases) /Ramakrishnan, Sathiya. January 2002 (has links) (PDF)
Thesis (M. Phil.)--University of Queensland, 2002. / Includes bibliographical references.
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Molecular mechanisms of alcohol tolerance in the fruit flyCowmeadow, Roshani Barbara, Atkinson, Nigel S., January 2004 (has links) (PDF)
Thesis (Ph. D.)--University of Texas at Austin, 2004. / Supervisor: Nigel S. Atkinson. Vita. Includes bibliographical references. Also available from UMI.
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Molecular padlock assay of crude plant leaf extracts for detection of listeria monocytogenes /Hurlburt, Allison L., January 2003 (has links) (PDF)
Thesis (M.S.) in Microbiology--University of Maine, 2003. / Includes vita. Includes bibliographical references (leaves 36-40).
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Molecular Padlock Assay of Crude Plant Leaf Extracts for Detection of Listeria MonocytogenesHurlburt, Allison L. January 2003 (has links) (PDF)
No description available.
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Molecular mechanisms of alcohol tolerance in the fruit flyCowmeadow, Roshani Barbara 28 August 2008 (has links)
Not available / text
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Molecular characterization of Sulfobacillus and related organismsSchutte, Mart-Alet (Martha Aletta) 03 1900 (has links)
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.
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The influence of nutrients and light on the metabolic activity and buyoancy of Microcystis aeruginosa and Anabaena circinalis / by Justin Dean Brookes.Brookes, Justin Dean January 1997 (has links)
Bibliography: leaves 252-267. / xvi, 267 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / These cyanobacteria are two freshwater phytoplankton which produce toxins, taint the taste and odour of potable water and form surface blooms. A technique was developed to assess cell metabolic activity and to determine the influence of light and nutrients on gas reside synthesis and bouyancy regulation in order to understand factors which favour their dominance, and thus how to control them. / Thesis (Ph.D.)--University of Adelaide, Dept. of Botany, 1998?
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Molecular analysis of an iron transporter gene of Burkholderia species MBA4Lin, Xiaohui, January 2009 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2009. / Includes bibliographical references (leaves 94-113). Also available in print.
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Molecular analysis of an iron transporter gene of Burkholderia species MBA4 /Lin, Xiaohui, January 2009 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2009. / Includes bibliographical references (leaves 94-113). Also available online.
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From osmolytes to diabetes : the impact of sugars and sugar alcohols on the cystic fibrosis pathogen, Burkholderia multivoransDenman, Carmen Cecile January 2013 (has links)
The incidence of CF related diabetes is on the rise as patient life expectancy continues to improve. Sugars elevated in diabetics include glucose, fructose, and mannose. These sugars, in addition to mannitol (recently approved as an inhaled osmolyte) are the basis for this study, aimed at assessing the impact these clinically relevant sugars have on virulence in Burkholderia multivorans. B. multivorans is a member of the Burkholderia cepacia complex (Bcc), and is the most frequent cause of Bcc infection in CF patients. Using an exopolysaccharide-deficient knockout in macrophage and Galleria mellonella infection models, biofilm formation, and adhesion assays, this study has identified exopolysaccharide-dependent and -independent phenotypes. Sequencing of B. multivorans C1576, a CF outbreak isolate, identified three putative adhesins in clinical isolate C1576 but not present in the sequenced environmental strain ATCC17616. Mannitol promoted adhesion and enhanced expression of these adhesins. This study characterised these adhesins and assessed the distribution within other clinical and environmental isolates of B. multivorans and the Bcc. Additionally, transcriptomic profiling of B. multivorans assessed the sugar response and EPS regulation during growth on clinically relevant sugars. Where possible, links were made between phenotypic studies and transcriptome data. B. multivorans EPS derived from fructose and mannitol was subjected to composition analysis using mass spectrometry, and assessed for biological activity. Still relevant to CF related diabetes, the ability of some members of the Bcc to bind insulin was assessed. Results indicated that a minority of strains bound insulin. Furthermore, by using flow cytometry cell sorting and fluorescence microscopy, results also showed only a small number of cells within a given population that bound insulin. In all, this study has added to the knowledge base of B. multivorans but more work is needed to fully understand virulence strategies exploited by this CF pathogen.
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