1H NMR of the isolated (R)-CHBE (500 MHz, CDCl3). Figures S3. 13C NMR of the isolated (R)-CHBE (126 MHz, CDCl3). (DOCX 1122 kb
Biosynthesis of diterpenoids with symbols indicating the chemical products (rectangles), enzymes (sh...
Additional file 1: Figure S1. NMR spectra of the product 6-hydroxynicotine. a 1H-NMR spectrum (CDCl3...
Pathways involving genes studied in this work. A schematic representation of (A) Sterol and caroteno...
Figure S3. 1H NMR spectrum (DMSO-d6, 400 MHz) of BII-Rafflesfungin. Figure S4. 13C NMR spectrum (DMS...
Figure S1. Determination of kinetic parameters of Debia-MDR with substrate acetone; Table S1. Specif...
Figure S1. NMR analysis of labda-13(16),14-dien-9-ol (compound 2) formed by the coupled reaction of ...
Figure S3. NMR analysis of 9,13-epoxy-labd-14-ene-19-ol (compounds 4/5) formed by the coupled reacti...
Additional file 6: Figure S4. HPLC spectra. (a) Spectra of the (R)-3,5-BTPE standard, (b) the 3,5-BT...
Figure S4. Mass spectrum of 3,4-DHPA transformed from 4-HPA by 4-HPA 3-hydroxylase. (DOCX 77 kb
In vivo characterization of MnPKS1 and MnPKS2 by coexpression with 4-coumaroyl-CoA ligase in Escheri...
Proton and carbon NMR spectral data of newly synthesized norcraugsodine and norbelladine. (DOCX 1738...
Figure S1. UV and ESI-MS spectra of SEK15b (3, a), chromomycin A3 (1, b) and chromomycin A2 (2, c). ...
Figure S1. 1H NMR of trifluoperazine metabolite; Figure S2. 2D HSQC NMR of trifluoperazine metabolit...
Figure S1 Experimental design of construction of a tyrosine high-producing platform. The overexpress...
Additional file 1: Figure S1. Schematic representation for generating of deletion mutants using the ...
Biosynthesis of diterpenoids with symbols indicating the chemical products (rectangles), enzymes (sh...
Additional file 1: Figure S1. NMR spectra of the product 6-hydroxynicotine. a 1H-NMR spectrum (CDCl3...
Pathways involving genes studied in this work. A schematic representation of (A) Sterol and caroteno...
Figure S3. 1H NMR spectrum (DMSO-d6, 400 MHz) of BII-Rafflesfungin. Figure S4. 13C NMR spectrum (DMS...
Figure S1. Determination of kinetic parameters of Debia-MDR with substrate acetone; Table S1. Specif...
Figure S1. NMR analysis of labda-13(16),14-dien-9-ol (compound 2) formed by the coupled reaction of ...
Figure S3. NMR analysis of 9,13-epoxy-labd-14-ene-19-ol (compounds 4/5) formed by the coupled reacti...
Additional file 6: Figure S4. HPLC spectra. (a) Spectra of the (R)-3,5-BTPE standard, (b) the 3,5-BT...
Figure S4. Mass spectrum of 3,4-DHPA transformed from 4-HPA by 4-HPA 3-hydroxylase. (DOCX 77 kb
In vivo characterization of MnPKS1 and MnPKS2 by coexpression with 4-coumaroyl-CoA ligase in Escheri...
Proton and carbon NMR spectral data of newly synthesized norcraugsodine and norbelladine. (DOCX 1738...
Figure S1. UV and ESI-MS spectra of SEK15b (3, a), chromomycin A3 (1, b) and chromomycin A2 (2, c). ...
Figure S1. 1H NMR of trifluoperazine metabolite; Figure S2. 2D HSQC NMR of trifluoperazine metabolit...
Figure S1 Experimental design of construction of a tyrosine high-producing platform. The overexpress...
Additional file 1: Figure S1. Schematic representation for generating of deletion mutants using the ...
Biosynthesis of diterpenoids with symbols indicating the chemical products (rectangles), enzymes (sh...
Additional file 1: Figure S1. NMR spectra of the product 6-hydroxynicotine. a 1H-NMR spectrum (CDCl3...
Pathways involving genes studied in this work. A schematic representation of (A) Sterol and caroteno...
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