Production of compounds derived from acetyl-coenzyme A
An acetyl coenzyme, compound technology, applied in the direction of adding compounds to stimulate growth, DNA/RNA fragments, recombinant DNA technology, etc., can solve problems such as the lack of metabolic switches
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Embodiment 5
[0084] Example 5 (below) and image 3 A explains the effect of pantothenate compound concentration in the medium on the production of HACD compounds in genetically modified host cells with high metabolic flux through the acetyl-CoA biosynthetic pathway to produce isoprenoid Farnesene. At low pantothenate levels (0.2 mg / L, <1% of the maximum pantothenate concentration tested), HACD compound production was essentially absent. Increased levels of pantothenate compounds were associated with increased production of HACD compounds prior to the flat-topping effect. Further increases beyond 1 mg / L pantothenate (10% of the maximum pantothenate compound concentration tested) resulted in no further increase in HACD compound production.
[0085] Notably, the growth of these cells showed an opposite trend to the production of HACD compounds. image 3 B illustrates the growth of the same strain at the same pantothenate concentration levels tested for HACD compound production. No or low ...
Embodiment 1
[0229] This example describes a method for determining the cell density (OD 600 ) Exemplary method.
[0230] Mix 8 μL of cell culture samples and 92 μL of Triton OD diluent (20g / L Triton X-114, 200mL / L PEG200, 200mL / L 100% ethanol, balance water) in a clean 96-well plate and stir the solution at 1,000RPM 6 minutes and the OD was determined by measuring the absorbance at 600 nm on an M5 spectrophotometer (Molecular Devices, Sunnyvale, CA). 600 .
Embodiment 2
[0232] This example describes an exemplary Nile Red-based method that can be used to determine farnesene titers in yeast cell cultures.
[0233] 98 μL of cell culture samples were transferred into 96-well black polystyrene flat bottom assay plates, and 2 μL of Nile Red (Invitrogen, Carlsbad, CA) dissolved in DMSO at 100 μg / mL was added to each well. Fluorescence levels were immediately measured on an M5 spectrophotometer with excitation at 500 nm and emission at 550 nm.
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