Warning: mkdir(): Permission denied in /websites/2010.igem.org/wiki/includes/GlobalFunctions.php on line 2176

Warning: wfMkdirParents: failed to mkdir "/websites/2010.igem.org/wiki/images/thumb/1/1f/Caltech_logo.png" mode 511 in /websites/2010.igem.org/wiki/includes/GlobalFunctions.php on line 2179
Team:Caltech/BBa K338004 - 2010.igem.org
 

Team:Caltech/BBa K338004

From 2010.igem.org


iGEM 2010



Home

People

Project Details

Protocols

Completed Systems

Notebook

Biosafety

Human Impact

References

Support


Caltech logo watermark.png

<partinfo>BBa_K338004 short</partinfo>

This is half of a planned part which would contain all three PHA synthase genes required to produce polyhydroxybutyrate (PHB) in cells: phaA, phaB1, phaC1. This half contains phaB1 and phaC1: <partinfo>BBa_K156013</partinfo> & <partinfo>BBa_K156014</partinfo>. It was designed to be ligated downstream of part BBa_K338003.

Usage and Biology

Design

When ligated downstream of BBa_K338003, the completed construct was designed to express all three PHA synthase genes required to make PHB oligomers from soybean oil. The three genes would be transcribed polycistronically on a single mRNA transcript under the IPTG-inducible control of the <partinfo>BBa_K215000</partinfo> promoter. Naturally, each gene is preceded by a standard RBS (<partinfo>B0034</partinfo>) and the transcript finishes with a strong terminator (<partinfo>B0015</partinfo>), for a total size of about 3500bp.

Note that these three genes should only cause the production of PHB oligomers in cells, not hardened plastic. A crosslinking agent is required to link the oligomers and form the final plastic product. Over-expression of the phaC1 gene could cause some crosslinking, but this has not been experimentally verified.

Literature

SY Lee describes how a similar gene construct (pSYL105) was used to produce very large amounts of PHB, up to 80-90% of the dry cell weight, under certain conditions. Synthesis of PHB is related to the amount of acetyl-CoA available - synthesis was bolstered in the presence of complex nitrogen sources, amino acids, or oleic acid. He also mentions that PHB production was highly dependent on the particular bacterial strain used. [10]

Characterization

Although not a finished product, it was tested in DH5α cells grown in 5mM glucose for 48 hours (5mL LB culture) at 37°C. The cells were then imaged at 100x, producing the following figures:

CaltechPlastic1.jpg

CaltechPlastic2.jpg

The small inclusion bodies suggest the production of an unknown, but possibly plastic-related, substance. The pSYL105 construct mentioned above also caused the formation of large inclusion bodies in cells that produced plastic, lending credence to this possibility.

 
Error creating thumbnail: Unable to create destination directory
Caltech footer.png


Locations of visitors to this page