Inducible expression vectors
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It is usually advantageous to keep a cloned gene represed until ready to express it.
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One reason is that eukaryotic proteins produced in large quantities in bacteria can be toxic.
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Even if these proteins are not actually toxic, they can build up to such great levels that they interfere with bacterial growth.
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In either case, if the cloned gene were allowed to remain turned on constantly, the bacteria bearing the gene would never grow to a great enough concentration to produce meaningful quantities of protein product.
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The solution is to keep the cloned gene turned off by placing it downstream of an inducible promoter that can be turned off.
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The lac promoter is inducible to a certain extent, presumably remaining off until stimulated by the synthetic inducer isopropylthiogalactoside (IPTG).
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Another strategy is to use a tightly controlled promoter as the λ phage promoter PL.
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Expression vectors with this promoter/operator system are cloned into host cells bearing a temperature-sensitive λ repressor gene (c1857).
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As long as these cells kept relatively low (32°C ), the repressor functions, and no expression takes place. However, when the temperature is raised to the nonpermissive level (42ºC), the temperature-sensitive repressor can no longer function and the cloned gene is induced.
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Last modified: Friday, 24 September 2010, 10:15 AM