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The Development of Protocols to Engineer and Screen Streptomyces in High Throughput to Test for the Activation of Cryptic Clusters by the Heterologous Expression of Pleiotropic Regulators

dc.contributor.advisorNodwell, Justin Ren_US
dc.contributor.advisorWright, Gerryen_US
dc.contributor.advisorLi, Yingfuen_US
dc.contributor.authorGverzdys, Tomas A.en_US
dc.contributor.departmentBiochemistryen_US
dc.date.accessioned2014-06-18T16:53:34Z
dc.date.available2014-06-18T16:53:34Z
dc.date.created2011-08-30en_US
dc.date.issued2011-10en_US
dc.description.abstract<p>The Gram-positive, soil dwelling bacteria of the genus <em>Streptomyces</em> produce greater than 50% of the clinically relevant antibiotics in use today. Thanks to the falling price of DNA sequencing, <em>Streptomyces</em> genomes are revealing that they encode more secondary metabolites (potential antibiotics) than they produce under standard laboratory conditions. By heterologously overexpressing the known pleiotropic regulators of antibiotic expression from <em>Streptomyces coelicolor</em> in several other <em>Streptomyces</em> species it has been shown that the secondary metabolite profile of these species can be influenced. While present-day methods of introducing genes (conjugation) and screening for antibiotics work well on a small scale, the low throughput nature of these protocols stand as a barrier to testing this hypothesis on a larger scale. The focus of the research presented here was to develop high throughput (HTP) methods of engineering and screening <em>Streptomyces</em>. With these two technologies in place, an attempt was to made to introduce three plasmids (pSET152-<em>ermE*</em>p-null, pSET152-<em>ermE</em>*p-<em>atrA</em> and pSET152-<em>ermE</em>*p-<em>lsr2<sub>NTD</sub></em>) into 120 wild-isolate <em>Streptomyces</em> species from the Wright Actinomycete Collection. Exconjugants were successfully obtained for all three plasmids in 48 species of <em>Streptomyces</em> and were screened for increased antimicrobial activity using a HTP, <em>lux</em>-based bioassay. Numerous strains showed increased antimicrobial activity but WAC00206, WAC00230 and WAC00263 with pSET152-<em>ermE</em>*p-<em>lsr2<sub>NTD </sub></em>showed the most promising improvement in antimicrobial activity. These hits have been designated as high priority for future investigation. These results suggest that HTP conjugation and the <em>lux</em>-based bioassay are powerful methods for introducing plasmids into and screening engineered streptomycetes.</p>en_US
dc.description.degreeMaster of Science (MSc)en_US
dc.identifier.otheropendissertations/6090en_US
dc.identifier.other7116en_US
dc.identifier.other2205330en_US
dc.identifier.urihttp://hdl.handle.net/11375/11095
dc.subjectluminescenceen_US
dc.subjectluxen_US
dc.subjectconjugationen_US
dc.subjectscreeningen_US
dc.subjectHTPen_US
dc.subjectHTSen_US
dc.subjectBiochemistryen_US
dc.subjectBiotechnologyen_US
dc.subjectBiochemistryen_US
dc.titleThe Development of Protocols to Engineer and Screen Streptomyces in High Throughput to Test for the Activation of Cryptic Clusters by the Heterologous Expression of Pleiotropic Regulatorsen_US
dc.typethesisen_US

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