Difference between revisions of "Part:BBa K196002"

Revision as of 21:53, 21 October 2009

HfsG protein from Caulobacter crescentus

Caulobacter crescentus is an aquatic, Gram-negative bacterium that divides asymmetrically. Besides the bacterium is able to synthesize a strong glue. This glue is mainly composed of polysaccharide. Different proteins are required in the holdfast synthesis, export and attachment in C.crescentus (for more details, please refer to the "introduction" section). In our project, we wanted to implement the glue production in Escherichia coli. As E. coli possesses homolog proteins, we decid to insert the hfsG and hfsH genes in a plasmid. HfsG is a glycosyltransferase and HfsH [1] is a carbohydrate esterase. Here is the BB for the hfsG gene.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
INCOMPATIBLE WITH RFC[25]
Illegal NgoMIV site found at 480
Illegal AgeI site found at 379
Illegal AgeI site found at 864
1000
COMPATIBLE WITH RFC[1000]

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 <partinfo>BBa_K196002 short</partinfo>
-<i>Caulobacter crescentus</i> is an aquatic, Gram-negative bacterium that divides asymmetrically and is able to synthetize a strong glue. This glue is mainly composed of polysaccharide. Different proteins are required in the holdfast synthesis, export and attachment in <i>C.crescentus</i> (for more details, please refer to the "introduction" section). In our project, we wanted to implement the glue production in <i>Escherichia coli/i>. As  <i>E. coli</i>  possesses homolog proteins, we decid to insert the hfsG and hfsH genes in a plasmid. HfsG is a glycosyltransferase and HfsH [https://parts.igem.org/Part:BBa_K196003:Design] is a carbohydrate esterase. Here is the BB for the hfsG gene.
+<i>Caulobacter crescentus</i> is an aquatic, Gram-negative bacterium that divides asymmetrically. Besides the bacterium is able to synthesize a strong glue. This glue is mainly composed of polysaccharide. Different proteins are required in the holdfast synthesis, export and attachment in <i>C.crescentus</i> (for more details, please refer to the "introduction" section). In our project, we wanted to implement the glue production in <i>Escherichia coli</i>. As  <i>E. coli</i>  possesses homolog proteins, we decid to insert the hfsG and hfsH genes in a plasmid. HfsG is a glycosyltransferase and HfsH [https://parts.igem.org/Part:BBa_K196003:Design] is a carbohydrate esterase. Here is the BB for the hfsG gene.
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