homology (68.3% aa identity) to the isoleucyl-tRNA synthetase gene from Thermotoga maritima. This gene is used in the taxonomic classification of microorganisms.
The pullulanase was amplified by PCR and cloned into 3 E. coli vectors with different promoters (trc and PL) and enhancing elements. These constructs were transformed into a number of E. coli host strains and expression levels using the different systems were compared. These results and the results from sequence alignments will be presented.
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