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<h1>Preliminary Team Project Description</h1> | <h1>Preliminary Team Project Description</h1> | ||
− | <b>ADaPtat1on : Expanding Toolkit for Acetinobacter baylyi</b> | + | <b>ADaPtat1on : Expanding Toolkit for <em>Acetinobacter baylyi</em></b> |
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<em>Acinetobacter baylyi</em> is a gram-negative, soil-dwelling, non-pathogenic, naturally competent and nutritionally versatile organism, known especially for its ability to degrade aromatic compounds. However, only a few tools are available for gene manipulation in Synthetic Biology experiments. This year, we plan to expand this toolkit for <em>A. baylyi</em> ADP1 by making synthetic promoter library along with codon optimized fluorescent reporter proteins for <em>A. baylyi</em> to achieve better control over expression rates. Codon usage table was also created by us using the genomic data. This can potentially open up various new exciting synthetic biology opportunities with this unexplored organism. | <em>Acinetobacter baylyi</em> is a gram-negative, soil-dwelling, non-pathogenic, naturally competent and nutritionally versatile organism, known especially for its ability to degrade aromatic compounds. However, only a few tools are available for gene manipulation in Synthetic Biology experiments. This year, we plan to expand this toolkit for <em>A. baylyi</em> ADP1 by making synthetic promoter library along with codon optimized fluorescent reporter proteins for <em>A. baylyi</em> to achieve better control over expression rates. Codon usage table was also created by us using the genomic data. This can potentially open up various new exciting synthetic biology opportunities with this unexplored organism. | ||
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Revision as of 06:15, 3 July 2018
Preliminary Team Project Description
ADaPtat1on : Expanding Toolkit for Acetinobacter baylyiAcinetobacter baylyi is a gram-negative, soil-dwelling, non-pathogenic, naturally competent and nutritionally versatile organism, known especially for its ability to degrade aromatic compounds. However, only a few tools are available for gene manipulation in Synthetic Biology experiments. This year, we plan to expand this toolkit for A. baylyi ADP1 by making synthetic promoter library along with codon optimized fluorescent reporter proteins for A. baylyi to achieve better control over expression rates. Codon usage table was also created by us using the genomic data. This can potentially open up various new exciting synthetic biology opportunities with this unexplored organism.