Paweł Górnaś, Krists Dukurs, Danija Lazdiņa, Inga Mišina, Elvita Bondarenko, Gundega Sebre, Sarmīte Strautiņa
Black currants (Ribes spp.) are rapidly expanding and growing genetic diversity demands analytical tools capable of high-throughput, robust screening of anthocyanin composition across large populations. Here, we report the development and extensive validation of an ultra-rapid (6 min), highly sensitive and reproducible RP-HPLC-DAD method based on a Kinetex EVO C18 column for the determination of major and minor anthocyanins in black currant. Application of this method to 415 genotypes - the most comprehensive screening to date - allowed accurate estimation of the proportional anthocyanin architecture, defined predominantly by delphinidin 3-O-rutinoside (44%), cyanidin 3-O-rutinoside (33%), delphinidin 3-O-glucoside (13%), and cyanidin 3-O-glucoside (6%). Notably, our data shows that petunidin 3-O-rutinoside was a considerable colorant in some genotypes, predominantly derived from the 'Ores × Ijunskaya Kondrashovoi' pedigree, indicating a lineage-specific diversification of the black currant anthocyanin profile. Collectively, the proposed method constitutes a strategic analytical tool for next-generation breeding and precision phenotyping of black currant anthocyanin profiles.