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Fig. 3 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 3. Expression of genes encoding glucosinolate biosynthetic enzymes correlates with product accumulation. Relative expression levels of selected genes encoding enzymes involved in the core glucosinolate biosynthesis were determined by RT-qPCR method using gene encoding actin as a reference. The obtained values were normalized by dividing each of them by the maximal value obtained for the tested gene in the respective species. Results are means ± SD from three independent experiments, each with four biological replicates (n = 12).

Fig. 1 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 1. General scheme of aliphatic and indolic glucosinolate biosynthesis. Dashed arrows represent multistage processes. GLs – glucosinolates, I3G – 3- indolylmethyl GL, 1OHI3G – 1-hydroxy-I3G, 4OHI3G – 4-hydroxy-I3G, 1MI3G – 1-methoxy-I3G, 4MI3G – 4-methoxy-I3G.

Fig. 5 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 5. Divergence of the CYP81F1/3/4 locus in the Camelineae species.Graphical representation of genomic regions containing putative CYP81F1, CYP81F3 and CYP81F4 orthologs in selected Brassicaceae plants. Roman numbers indicate chromosome numbers (if available). Gene orientations are indicated by arrows.

Fig. 8 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 8. IGMT phylogenetic tree is incongruent with the phylogeny of the investigated species. A neighbor-joining phylogenetic tree of IGMT proteins from the investigated species. A. thaliana O-methyltransferase 1 (AtOMT1) was used as an outgroup. The bar represents 10% sequence divergence.

Fig. 7 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 7. Divergence of the IGMT1-4 locus in the Camelineae species. Graphical representation of genomic regions containing putative IGMT1-4 orthologs in selected Brassicaceae plants. Roman numbers indicate chromosome numbers (if available). Gene orientation are indicated by arrows.

Fig. 2 in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 2. Total accumulation of glucosinolates varies strongly between particular organs and between investigated species. Bar graphs indicate total peak areas of AG and IG molecular ions obtained during LC/MS analysis. The results and are means ± SD from three independent experiments with three biological replicates in each (n = 9). Significantly different statistical groups indicated by ANOVA (P <0.05, Tukey's test) are shown with upper-case (AGs) and lowercase (IGs) letters. AGs – aliphatic glucosinolates, IGs – indolic glucosinolates; # - not detected

Fig. 4. The investigated Camelineae species differ from A in Evolutionary changes in the glucosinolate biosynthetic capacity in species representing Capsella, Camelina and Neslia genera

Fig. 4. The investigated Camelineae species differ from A. thaliana in their glucosinolate modification capacity. Bar graphs indicate peak areas of particular molecular ions corresponding to methylsulfinylalkyl-aliphatic glucosinolates (AGs) and to indolic glucosinolates (IGs) detected during LC/MS analysis in siliques, inflorescences and roots of mature plants. The obtained values are means ± SD from three independent experiments with three biological replicates in each (n = 9). MeSO – methylsulfinylalkyl, GL – glucosinolate, I3G – 3-indolylmethyl GL, 1MI3G – 1-methoxy-I3G, 4OHI3G – 4-hydroxy-I3G, 4MI3G – 4-methoxy-I3G, # - not detected

closedIPD-NOFeb 2026View details →

ClinicalTrials.gov32/100

Effects of Camelina Sativa Oil in Free-living Older Adults

ClinicalTrials.gov study NCT04965948. IPD Sharing: NO. Countries: 1. Publications: 1.

opencc-by-4.0Jan 2024View details →

supplemental files for Assembly and analysis of sequence from a spring and winter type Camelina sativa by whole genome PacBio HiFi technologies

Supplemental files for Assembly and analysis of sequence from a spring and winter type Camelina sativa by whole genome PacBio HiFi technologies

opencc-by-4.0Jan 2019View details →

Figure 3 from: Brock JR, Mandáková T, Lysak MA, Al-Shehbaz IA (2019) Camelina neglecta (Brassicaceae, Camelineae), a new diploid species from Europe. PhytoKeys 115: 51-57. https://doi.org/10.3897/phytokeys.115.31704

Figure 3 Trichomes of lowermost part of stem in Camelinaneglecta. Greenhouse-grown plants from seeds of Besancon s.n. (USDA accession 650135). Scale bar: 400 μm.

opencc-by-4.0Jan 2019View details →

Figure 2 from: Brock JR, Mandáková T, Lysak MA, Al-Shehbaz IA (2019) Camelina neglecta (Brassicaceae, Camelineae), a new diploid species from Europe. PhytoKeys 115: 51-57. https://doi.org/10.3897/phytokeys.115.31704

Figure 2 Mitotic chromosomes of Camelinaneglecta. Greenhouse-grown plants from seeds of Besancon s.n. (USDA accession 650135). Scale bar: 10 μm.

opencc-by-4.0Jan 2019View details →

Figure 4 from: Brock JR, Mandáková T, Lysak MA, Al-Shehbaz IA (2019) Camelina neglecta (Brassicaceae, Camelineae), a new diploid species from Europe. PhytoKeys 115: 51-57. https://doi.org/10.3897/phytokeys.115.31704

Figure 4 SEM image of Camelinaneglecta seed. Greenhouse-grown plants from seeds of Besancon s.n. (USDA accession 650135). Scale bar: 1 mm.