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. 2014 Aug 8;26(8):3403–3415. doi: 10.1105/tpc.114.124776

Table 1. Relative Quantification of Aromatic Amino Acids, Phenolics, Anthocyanins, and Glycoalkaloids in Semi-Polar Extracts of ABCG1-RNAi and Control Periderm.

Compound Log2(Peak Area/Fresh Weight) Median ± sd
Control ABCG1-RNAi
Phe 11.9 ± 0.5 9.9 ± 0.8***
Tyr 12.5 ± 0.4 11.7 ± 1.0***
Trp 11.8 ± 0.4 11.4 ± 1.1
Caffeic acid 9.6 ± 0.9 6.7 ± 1.6***
Chlorogenic acid 14.2 ± 0.3 12.8 ± 0.6***
Cinnamoyl putrescine n.d. 9.5 ± 1.3
Coumaroyl putrescine n.d. 10.9 ± 1.5
Caffeoyl putrescine 7.4 ± 0.5 14.4 ± 1.4***
Dihydrocaffeoyl putrescine 7.0 ± 0.7 14.3 ± 1.9***
Feruloyl putrescine 9.8 ± 0.6 14.9 ± 1.0***
Dihydroferuloyl putrescine 9.7 ± 0.6 12.2 ± 1.0***
Vanilloyl putrescine 7.7 ± 0.3 9.3 ± 0.5***
Feruloyl tyramine (FT) 9.1 ± 0.5 8.3 ± 0.9***
Feruloyl octopamine (FO) 9.0 ± 1.1 9.5 ± 1.3
FT-FT dehydrodimer 5.4 ± 0.8 12.7 ± 0.8***
FT-FO dehydrodimer n.d. 10.4 ± 1.0
Pelargonidin-3-(coumaroyl-Rha-Glc)-5-Glc 11.3 ± 0.9 9.5 ± 2.0***
Pelargonidin-3-(feruloyl-Rha-Glc)-5-Glc 9.7 ± 0.7 8.4 ± 2.0***
α-Chaconine 13.6 ± 0.3 13.2 ± 1.2**
α-Solanine 10.6 ± 0.4 10.2 ± 1.0**

Methanolic extracts of ABCG1-RNAi (line N [n = 8], line P [n = 8], line B [n = 8], line F [n = 8]) and control (wild type [n = 8] and empty vector [n = 8]) tuber periderm were prepared and analyzed by UPLC/PDA/ESI(+)-QTOFMS. Target compounds were relatively quantified using quantifier ions/retention times from Supplemental Table 11. Resulting peak areas were normalized to fresh weight and log2 transformed. Values shown represent medians ± sd. Significance analysis of differences between ABCG1-RNAi and control was performed by t test (two-tailed, unequal variances): *P ≤ 0.05, **P ≤ 0.01, and ***P ≤ 0.001. n.d., not detectable.