Team:Edinburgh/Plan/StarchSynthesis

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=== Starch synthesis ===
=== Starch synthesis ===
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The second phase is the conversion of glycogen to starch. To achieve this we are creating isoamylase and granule-bound starch synthesase BioBricks (''isa1'', ''isa2'' and ''gbss'') from ''Zea mays'' cDNAs. These three genes together should be sufficient for the production of starch from glycogen.
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Starch is composed of amylopectin, a polyglucan linked by α-1,4 and α-1,6 bonds, and amylose, a derivative of amylopectin with fewer α-1,6 linkages and thus a more linear structure. Synthesising starch from glycogen requires just a few steps and genes:
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* '''''SU1''''' (isoamylase 1) from ''Zea mays''. This associates with isoamylase 2 and together they are responsible for the conversion of glycogen to amylopectin. We decided to use an isoamylase from a plant that naturally accumulates a lot of starch, and it was for this reason that we settled on ''Z. mays''.
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* '''''ISO2''''' (isoamylase 2) from ''Zea mays''. This associates with SU1 to convert glycogen to amylopectin.
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* '''''GBS1''''' (granule-bound starch synthase) from ''Arabidopsis thaliana''. This converts some amylopectin into amylose, and thus is responsible for the final step in starch production. It also compacts the starch into a intracellular granule.
== Overview ==
== Overview ==

Revision as of 15:38, 28 October 2008

Contents

Starch synthesis

Glucose must be taken up by the cells and synthesised first into glycogen and then starch.

Genes

Figure 1: The native glycogen synthesis pathway of E. coli. In blue is glgC, a gene which we have mutated to a more active form.

Glycogen synthesis

E. coli and B. subtilis are natively able to synthesise glycogen from starch (see Figure 1 for E. coli's native pathway). However, we want to upregulate this pathway:

  • The gene glgC (ADP-glucose pyrophosphorylase, catalysing the convertion glucose 1-phosphate and ATP to ADP-glucose and PPi) is responsible for the most rate-limiting step of glycogen synthesis in E. coli. This is because the protein is negatively regulated by 5'-AMP, ADP or orthophosphate. The glgC16 mutant has the substitution G336D to glgC, and has been reported to increase the yield of glycogen. This is due in part to the loss of allosteric inhibition and is also due to increased activity in the absence of its activator molecule, fructose 1,6 bis-phosphate.

Starch synthesis

Starch is composed of amylopectin, a polyglucan linked by α-1,4 and α-1,6 bonds, and amylose, a derivative of amylopectin with fewer α-1,6 linkages and thus a more linear structure. Synthesising starch from glycogen requires just a few steps and genes:

  • SU1 (isoamylase 1) from Zea mays. This associates with isoamylase 2 and together they are responsible for the conversion of glycogen to amylopectin. We decided to use an isoamylase from a plant that naturally accumulates a lot of starch, and it was for this reason that we settled on Z. mays.
  • ISO2 (isoamylase 2) from Zea mays. This associates with SU1 to convert glycogen to amylopectin.
  • GBS1 (granule-bound starch synthase) from Arabidopsis thaliana. This converts some amylopectin into amylose, and thus is responsible for the final step in starch production. It also compacts the starch into a intracellular granule.

Overview