Article ID Journal Published Year Pages File Type
6396376 Food Research International 2014 6 Pages PDF
Abstract

•Content of diterpenes was differentiated among traditional and modern cultivars.•Modern crosses presented higher kahweol/cafestol ratio than traditional cultivars.•Modern crosses have higher antioxidant activity.

Genetic improvement of coffee is aimed at transferring disease resistance genes from Coffea canephora to Coffea arabica cultivars, but the composition of arabica coffee could be affected by the introgression of genetic material from canephora. The objective of the this work was to compare traditional Brazilian arabica coffee cultivars (Bourbon, Catuaí, and Icatu) with modern arabica cultivars (IAPAR 59, IPR 98, IPR 99, and IPR 103) produced in the same edapho-climatic conditions. The cultivation, harvesting, post-harvesting and roasting processes were standardized to evaluate the influence of genetic diversity on the composition of bioactive compounds (5-caffeoylquinic acid, trigonelline, nicotinic acid, caffeine, cafestol, kahweol, and melanoidins) and antioxidant activity (AA) of the roasted coffees. Compositional variability among the coffee cultivars studied was observed, mainly with regard to contents of 5-caffeoylquinic acid (5-CQA) (from 936 to 1695 mg 100 g− 1), cafestol (from 414 to 742 mg 100 g− 1), and kahweol (from 439 to 1068 mg 100 g− 1). In general, arabica cultivars with the introgression of C. canephora genes showed high antioxidant activity and differed from coffees of traditional arabica genotypes mainly in terms of their diterpenes profiles. A high correlation was observed among the AA (assessed by different methods) and some of the bioactive compounds (melanoidins, caffeine, and 5-CQA). Variability in the levels of the bioactive compounds was higher than that the observed for AA (from 4.2 to 4.7 g gallic acid 100 g− 1 by Folin-Ciocalteau reducing capacity, from 3.75 to 5. 42 g Trolox 100 g− 1 coffee by ABTS radical scavenging activity, and from 80.1 to 83.0 percentage of inhibition of autoxidation of linoleic acid).

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