Coffee Diterpenes: before Harvesting the Bean to your Cup
Fábio Junior Moreira Novaes*
Universidade Federal do Rio de Janeiro, Brazil
Submission: May 25, 2018;Published: July 17, 2018
*Corresponding author: Novaes FJM, Universidade Federal do Rio de Janeiro, Instituto de Química, Laboratório de Análise de Aromas, Avenida Athos da Silveira Ramos, 149, Bloco A, Sala 626, Rio deJaneiro, RJ 21941-895, Brazil; Tel: +55 21 3938-7121; Email: email@example.com
How to cite this article: Novaes FJM, Coffee Diterpenes: before Harvesting the Bean to your Cup. Nutri Food Sci Int J. 2018; 7(2): 555706. DOI:10.19080/NFSIJ.2018.07.555706.
Cafestol and kahweol are molecules that exist only in coffee beans, even though they are also available for each consumer of the coffee beverage. Endogenous coffee enzymes and the absence of these molecules in other matrices confer them the title of taxonomic markers of plants of the genus Coffee. The trajectory of these molecules initiates with their biosynthesis and accumulation in the coffee fruit, passes through transformations during the storage and roasting of beans, reaches their transference to the beverage and ends when the human organism absorbs and metabolizes them. The present work deals with the chemical transformations imposed on these molecules during their trajectory in the coffee commercial cycle, as well as aspects related to human health.
Coffee is one of the most consumed beverages in contemporary society. About 80% of the world's adult population appreciates the beverage, which is usually marketed in the form of blends between Coffea arabica L. and C. canephora P. . Due to the great popular appreciation, coffee has been the object of studies within the Food Sciences, some directly related to its chemical composition [2-4].
In the last three decades, studies related to the diterpenic composition of coffee bean gained attention. Two main factors contributed to this interest. The first was related to the representative presence of cafestol and kahweol (C&K) derivates (Figure 1) in the beans (≤2.5% w/wof its dry mass) and in its lipid fraction (≤20 % w/w) [5,6], and the second their anti-carcinogenic, antioxidant, anti-inflammatory and hypercholesterolemic activities [7-13].
The coffee tree biogenetically modifies the ent-kaurane skeleton to produce C&K and distributes them throughout the plant as dialcohols (free form), ethers or esters (Figure 1) . They are found in all the main tissues of the shrub (roots, branches, leaves and fruits), but mainly in coffee fruits, where their amount is dependent on the fruit stage of maturity . Cafestol is the most common coffee diterpene in not only the major commercial species, C. arabica and C. robusta, but also in wild coffee . The Arabica coffee beans have kahweol:cafestol proportions between 1:2 and 2:1, and this ratio is a coffee quality parameter for the beverage . Kahweol may be absent in robusta coffee, or present in very low concentrations (≤0.01% w/w) . Kahweol differs from cafestol by an unsaturation present in the ring A of the diterpene nucleus, between carbons 1 and 2 (Figure 1). The Robusta coffee has also ethers derived from C&K on carbon 16 (Figure 1) . The presence and the ratio between Kahweol and 16-O-methyl-cafestol, when applied in a polynomial equation, can discriminate between different blend proportions of Arabica and Robusta beans in mixtures .
Commercial and wild coffee species have the esterified
diterpenes in a proportion greater (250-fold) than their
respective alcohols (Figure 1) [5-6]. However, according to
SCOPUS database, there are few articles dealing with these
compounds: only 16papers compared to 362 for the free form
of the dialcohol . This is probably due to the dispersion
of C&K into 24 esters of different chain lengths and degrees
of unsaturation (Figure 1), and the absence of effective
techniques to obtain them individually [3,19-21]. For this
reason, the research is concentrated on the free form of C&K
after hydrolysis of their respective esters, simplifying their
determination in coffee matrices and increasing the bulk of
these diterpenes for further studies.
When the green (or raw) coffee beans are stored, there is an
increase in the content of both free form of C&K and fatty acids.
Endogenous lipases in the beans hydrolyze the ester forms of
these diterpenes (Figure 1) and the acylglycerol derivatives
[22,23]. When the green bean is submitted to the roasting
conditions (180-265 °C / 2-21min), C&K lose water generating
several dehydrocafestol and dehydrokahweol, respectively,
as well as the ether and aldehyde derivatives [22,24]. The
amounts of both compounds increase proportionally with
raising roasting temperatures or time of exposition. The
cafestol/dehydrocafestol ratio is a good indicator of the coffee
roasting degree . Values below 15 for this ratio signal dark
roasted coffee and values between 15 and 25 indicate medium
roasting. Values above 25 describe a light-roasted coffee
The C&K extraction from roasted and grounded beans
happens during the coffee beverage preparation. However,
the final C&K concentration in the beverage is dependent on
the kind of extraction procedure employed. The boiled coffee
beverage - Scandinavian-type - reaches up to 1.766mg L-1 of
C&K, whereas in beverages prepared with paper filter, C&K are
widely retained, and their concentration reaches only 2.4mg
L-1 after the percolation of these compounds through the paper
When ingested by humans, about 70% of the total coffee
diterpenes are absorbed in the intestinal tract, whereas 24%
are degraded in the stomach and only 1% is excreted in the
urine after conjugation with glucuronic acid and sulfate salts
[15,29]. Results in rats indicate the presence of C&K esters in
the body for 5 to 10 days after its administration, whereas the
hydrolyzed forms persist for less than 48h . These findings
show that the hydrocarbon chain of the esterified coffee
diterpenes increases their lipossolubility and the residence
time in the tissues, which, therefore, increases their active
period in the organism. Therefore, the investigations should
be directed to the esterified forms, unless these esters are
hydrolyzed in the human organism, releasing the free form.
The present work discussed the trajectory of coffee
diterpenes - cafestol and kahweol - on the molecular level
intheir environment/food/man relationship. It initiates with
C&K biosynthesis in the plant, followed by their concentration
in the coffee fruit, until their absorption in and elimination
from the human organism. This multidisciplinary approach
opens perspectives for several studies on these molecules and
their derivatives along the coffee commercial path that ends
with its consumption.
The author thanks CAPES, CNPq and FAPERJ agencies for
funding and the editorial staff of NFRIJ for the invitation to
write this article. The author also thanks Dr. Claudia Moraes
de Rezende and Dr. Ademario Iris da Silva Junior for their kind
scientific and English revision of the manuscript.