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3.1.3.37: sedoheptulose-bisphosphatase

This is an abbreviated version!
For detailed information about sedoheptulose-bisphosphatase, go to the full flat file.

Word Map on EC 3.1.3.37

Reaction

sedoheptulose 1,7-bisphosphate
+
H2O
=
sedoheptulose 7-phosphate
+
phosphate

Synonyms

At3g55800, BiBPase, bifunctional fructose-1,6-bisphosphatase/sedoheptulose-1,7-bisphosphatase, dual-function fructose-1,6/sedoheptulose-1,7-bisphosphatase, FBP/SBPase, FBPase/SBPase, fructose -1,6-/sedoheptulose-1,7-bisphosphatase, fructose-1,6-/sedoheptulose-1,7-bisphoshatase, fructose-1,6-/sedoheptulose-1,7-bisphosphatase, fructose-1,6-biphosphatase/sedoheptulose-1,7-biphosphatase, fructose-1,6/sedoheptulose-1,7-bisphosphatase, GlpXp, More, ore, Os04g0234600, phosphatase, sedoheptulose di-, SBPase, SBPase3, SebP1, SED(1,7)P2ASE, sedoheptulose 1,7-bisphosphatase, sedoheptulose 1,7-diphosphatase, sedoheptulose 1,7-diphosphate phosphatase, sedoheptulose bisphosphatase, sedoheptulose diphosphatase, sedoheptulose-1,7-bisphosphatase, sedoheptulose-1-7 bisphosphatase, Sedoheptulose-bisphosphatase, SedP2-ase, seduheptulose bisphosphatase, SYNPCC7002_A1301, tll1276

ECTree

     3 Hydrolases
         3.1 Acting on ester bonds
             3.1.3 Phosphoric-monoester hydrolases
                3.1.3.37 sedoheptulose-bisphosphatase

Application

Application on EC 3.1.3.37 - sedoheptulose-bisphosphatase

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APPLICATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
biofuel production
engineered cyanobacteria with enhanced growth show increased ethanol production and higher biofuel to biomass ratio. Speeding up the Calvin-Benson-Bassham cycle theoretically has positive effects on the subsequent growth and/or the end metabolite(s) production. Four Calvin-Benson-Bassham cycle enzymes, ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO), fructose-1,6/sedoheptulose-1,7-bisphosphatase (FBP/SBPase), transketolase (TK) and aldolase (FBA) are selected to be cooverexpressed with the ethanol synthesis enzymes pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH) in the cyanobacterium Synechocystis PCC 6803. An inducible promoter, PnrsB, is used to drive pyruvate decarboxylase and alcohol dehydrogenase expression. When PnrsB is induced and cells are cultivated at 0.065 mM photons/m*s, the RuBisCO-, FBP/SBPase-, TK-, and FBA-expressing strains produce 55%, 67%, 37% and 69% more ethanol and 7.7%, 15.1%, 8.8% and 10.1% more total biomass (the sum of dry cell weight and ethanol), respectively, compared to the strain only expressing the ethanol biosynthesis pathway. The ethanol to total biomass ratio is also increased in Calvin-Benson-Bassham cycle enzymes overexpressing strains. Using the cells with enhanced carbon fixation, when the product synthesis pathway is not the main bottleneck, can significantly increase the generation of a product (exemplified with ethanol), which acts as a carbon sink
biotechnology