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Table 1.

Strains used in this study.

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Figure 1.

The engineered taxadiene biosynthetic pathway in S. cerevisiae.

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Figure 2.

Production of taxadiene by engineered S. cerevisiae strains SyBE_001188, SyBE_001189, SyBE_001190 and SyBE_001110.

Data are represented as mean value of production from three independent fermentations.

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Figure 2 Expand

Figure 3.

Docking result of FPP with (A) GGPPSbc; (B) GGPPSgb; (C) GGPPSrc; (D) GGPPSeh; (E) GGPPScr; (F) GGPPSsc.

In A-F, the left figure represent the whole protein-substrate docking; the right figure is site gain.

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Figure 3 Expand

Table 2.

Data of enzyme-substrate docking.

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Table 2 Expand

Figure 4.

Production of taxadiene by engineered S. cerevisiae strains SyBE_001109, SyBE_001110, SyBE_001111, SyBE_001113, SyBE_001114, and SyBE_001115.

Data are represented as mean value of production from three independent fermentations.

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Figure 4 Expand

Figure 5.

The contents of identified metabolites and amino acids in glycolytic pathway and TCA cycle of W303-1A and YSG50.

The y-axis was relative abundance which was calculated by normalization of peak area of each metabolite to internal standard, and each value represented mean value of two independent replicates.

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Figure 5 Expand

Figure 6.

The relative abundance of TCA cycle intermediates (citrate, succinic acid and fumaric acid) in taxadiene producing yeast SyBE_001113, SyBE_001114, and SyBE_001115 compared with those in YSG50 chassis.

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Figure 6 Expand