Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2016 May 6.
Published in final edited form as: Acta Hortic. 2015 Jan 12;1061:219–224. doi: 10.17660/ActaHortic.2015.1061.24

Fruit Composition of Elderberry (Sambucus spp.) Genotypes Grown in Oregon and Missouri, USA

P Perkins-Veazie 1, AL Thomas 2, PL Byers 3, CE Finn 4
PMCID: PMC4859753  NIHMSID: NIHMS782345  PMID: 27158182

Abstract

Twelve Sambucus nigra subsp. canadensis genotypes were grown at two Missouri and one Oregon (USA) locations to characterize fruit composition in 2004, 2005, and 2006. Fruit was also sampled from an additional 10 genotypes of subsp. canadensis and nigra grown in Oregon. Soluble solids content ranged from 8.9 to 12.5 °Brix, and titratable acid (as citric acid) was 0.4 to 1.7 g/100ml. Ferric ion reducing activity potential (FRAP) values were 15.6 to 30.7 μmol/g trolox equivalents. Total anthocyanin content ranged from 85 to 385 mg/100 g cyanidin-3-glucoside equivalents (C3GE) and total phenolic content was 421 to 719 mg/100 g gallic acid equivalents (GAE). Of the genotypes sampled in three locations, six genotypes were high (250-350), and four were very low in total anthocyanin (<150 mg/100 g C3GE), respectively. ‘Barn’ and ‘Scotia’ were highest, and ‘Nova’ lowest in total anthocyanin content among genotypes grown in Oregon. Of the total antioxidant tests used, total phenolics was the best quick test, as it is the easiest of the assays, showed the least change among years, and correlated highly with FRAP.

Keywords: anthocyanin, phenolics, antioxidant, acidity, FRAP, trolox

INTRODUCTION

While the European elderberry (Sambucus nigra L. subsp. nigra) is well known and cultivated domestically in Europe and elsewhere, the native North American elderberry [Sambucus nigra L. subsp. canadensis (L.) Bolli] is a niche crop (Charlebois et al., 2010). The unique anthocyanins in both subspecies (cyanidin sambubiosides) have generated interest for use in pharmaceuticals and dietary supplements (Mohebalian et al., 2012). Elderberries possess anti-inflammatory and anti-viral properties (Zakay-Rones et al., 1995; Roschek et al., 2009). Additionally, the acylated anthocyanins common in American elderberry are prized for imparting color stability to food products (Nakatani et al., 1995; Lee and Finn, 2007). In this paper, we examine the fruit composition characteristics of elderberries grown in diverse geographic locations.

MATERIALS AND METHODS

Plantings of 12 American elderberry genotypes were established in 2003 at three U.S. locations: Mt. Vernon, Missouri (latitude 37°4’N; longitude 93°53’W), Mountain Grove, Missouri (latitude 37°13’N; longitude 92°26’W), and Corvallis, Oregon (latitude 44°30’N; longitude 123°28’W). Orchard and experimental details, including genotypes, sites, environmental conditions, horticultural methods, harvest protocols, etc. are described in Thomas and Byers (2000), Finn et al. (2008) and Thomas et al. (2013). Fruit from replicated plots at the three sites was harvested 2004, 2005, and 2006. An additional 10 genotypes were sampled from Corvallis in 2004 and 2005. All fruit was harvested at peak ripeness, frozen, and held at −20°C until analyzed at the former USDA-ARS Wes Watkins Agricultural Research Laboratory, Lane, OK.

About 50 g berries were destemmed and thawed, pureed with double distilled water (1:1 wt./volume) using a blender cup, then ground and homogenized. Soluble solids content (SSC; °Brix) pH, titratable acidity, total anthocyanin and total phenolics content were measured as outlined in Thomas et al. (2013). Ferric reducing activity potential using trolox substrates was measured on the same extracts used for total phenolics following methods of Benzie and Strain (1999).

Data were subjected to analysis of variance (Proc GLM; SAS Institute, Cary, NC) and means separated by least significant difference test at p ≤ 0.05. Linear regression was performed using SAS to determine relationships between compositional assays.

RESULTS AND CONCLUSION

When averaged across locations in all years, genotypes varied in all fruit composition characteristics evaluated (Table 1). The pH, SSC, and acidity of elderberry genotypes grown in the three locations averaged 4.92, 10.9 °Brix, and 0.53 g/100 ml citric acid, respectively. Among genotypes grown at all locations, ‘Highway O’ and ‘Johns’ were highest in pH, but low to lowest in SSC and acidity. ‘Johns’ and ‘Netzer’ were consistently low in anthocyanin content, appearing brown in color (Thomas et al., 2013). This effect was also seen in total phenolics content, where ‘Johns’ and ‘Netzer’ were lowest (439 and 514 mg/100 g, respectively) while ‘Adams 2′ was highest (719 mg/100 g). Lee and Finn (2007) also reported high total anthocyanin and phenolic values for ‘Adams 2′. The canadensis genotypes used in this study were found to be somewhat lower in total anthocyanins compared with values reported for nigra by Veberic et al. (2009).

Table 1.

Fruit composition of twelve American elderberry genotypes, averaged across three U.S. locations and three harvest seasons (2004-2006); portions of this table excerpted from Thomas et al. (2013) for comparison.

Genotype n pHz SSC
(°Brix)
TA
(g/100 ml citric acid)
Total anthocyanins
(mg/100 g C3GE)
Total phenolics
(mg/100 g GAE)
FRAP
(μmol/g trolox equiv.)
Adams 2 41 4.90 cdy 11.8 ab 0.58 abc 312 ab 719 a 30.7 a
Bob Gordon 41 4.86 cde 11.1 c 0.55 c 334 a 649 b 27.6 bc
Competition 5 35 4.73 g 12.2 a 0.60 a 224 c 609 de 25.3 de
Eridu 1 35 4.77 fg 11.3 c 0.59 ab 328 ab 642 bc 26.3 cd
Gordon E 36 4.82 ef 11.3 bc 0.49 ef 246 c 587 ef 18.7 g
Harris 4 35 4.84 def 9.9 d 0.58 abc 300 b 616 d 23.2 f
Highway O 29 5.19 a 9.3 e 0.47 f 315 ab 604 de 23.8 ef
Johns 39 5.17 a 10.4 d 0.42 g 105 e 439 i 12.9 i
Netzer 38 4.91 c 12.2 a 0.56 bc 116 e 514 h 15.8 h
Votra 35 5.04 b 10.4 d 0.46 f 237 c 561 g 18.2 g
Walleye 30 5.01 b 11.1 c 0.51 de 156 d 564 fg 15.6 h
Wyldewood 35 4.83 def 9.4 e 0.53 d 313 ab 622 cd 28.0 b

Overall mean 429 4.92 10.9 0.53 250 595 22.3
z

Abbreviations: SSC=soluble solids concentration; TA=titratable acidity; C3GE=cyanidin-3-glucoside equivalents; GAE=gallic acid equivalents; FRAP=ferric reducing activity potential.

y

Means within columns with the same letters are not significantly different according to the least significant difference (LSD) test (p ≤ 0.05).

Genotypes with the highest FRAP values were ‘Adams 2′, ‘Wyldewood’, ‘Bob Gordon’, and ‘Eridu 1′. The first three are commercially-available cultivars, and these results support their value as cultivars for use in dietary supplements and other products. ‘Johns’, another commercial cultivar, had very low FRAP values. As reported in Thomas et al. (2013), ‘Johns’ productivity was poor at both Missouri sites. The poor productivity plus poor fruit composition of ‘Johns’ makes it an unsuitable cultivar for the midwestern US.

Of the elderberries grown only in Oregon, pH, SSC, and acidity ranged from 4.03 to 4.75; 8.9 to 12.5 °Brix; and from 0.73 to 1.65 g/100 ml, respectively (Table 2). The genotypes ‘Haschberg’, ‘Korsør’, and ‘Golden City’ were low in pH and high in acidity while SSC was highest in ‘Barn’, ‘Scotia’, and ‘Korsør’. Total anthocyanin content ranged widely, from 85 to 385 mg/100 g. ‘Barn’ was high in total anthocyanin, phenolic, and FRAP values. In contrast, ‘York’ and ‘Nova’ were low in total anthocyanin and FRAP values relative to the other genotypes. The representation of nigra genotypes in this study was small but indicates that both subspecies may have similar processing characteristics when cultivated in Oregon.

Table 2.

Mean fruit composition of elderberries grown at Corvallis, OR in 2004 and 2005.

Genotype n pHz SSC
(°Brix)
TA
(g/100 ml citric acid)
Total anthocyanins
(mg/100 g C3GE)
Total phenolics
(mg/100 g GAE)
FRAP
(μmol/g trolox equiv.)
Subsp. canadensis
Adams 1 16 4.32 bcdy 10.1 bc 1.12 cd 291 bc 559 b 23.4 b
Barn 6 4.30 bcd 12.5 a 1.07 de 385 a 672 a 31.7 a
Golden City 8 4.16 dce 10.9 ab 1.29 bc 234 cd 525 bcd 21.2 b
Maxima 10 4.37 de 10.7 abc 0.92 de 166 de 546 bc 21.9 b
Nova 10 4.75 a 10.2 bc 0.76 deb 85 f 421 d 14.0 c
Scotia 12 4.49 ab 11.0 ab 0.91 e 323 ab 532 bc 24.6 b
York 13 4.72 a 10.5 bc 0.73 e 121 ef 443 cd 13.7 c

Mean 4.60 11.0 0.84 193 518 20.2

Subsp. nigra
Haschberg 8 4.03 e 8.9 c 1.65 a 233 cd 497 bcd 26.4 ab
Korsør 18 4.08 de 11.0 ab 1.38 b 191 de 500 bcd 23.0 b
CSAM14 6 4.22 cde 9.4 bc 1.61 a 189 de 542 bc 24.0 b

Mean 4.35 10.6 1.27 207 521 22.4
z

Abbreviations: SSC=soluble solids concentration; TA=titratable acidity; C3GE=cyanidin-3-glucoside equivalents; GAE=gallic acid equivalents; FRAP=ferric reducing activity potential.

y

Means within columns with the same letters are not significantly different according to the least significant difference (LSD) test (p ≤ 0.05).

When total anthocyanin or total phenolic contents were regressed to FRAP values, strong linear relationships were seen among these variables (Fig. 1). Regression fit was similar between total anthocyanin and FRAP (r2=0.66), total phenolic content and FRAP (r2=0.63), and total anthocyanin and total phenolic content (r2=0.61).

Fig. 1.

Fig. 1

(A) Regression of total monomeric anthocyanin content to trolox values, (B) regression of total phenolic content to trolox values, (C) regression of total monomeric anthocyanin to total phenolic content, all across multiple elderberry genotypes and locations.

Results from this study support earlier findings (Finn et al., 2008; Özgen et al., 2010; Thomas et al., 2013) that the fruit composition character of elderberry is influenced by both genetic and environmental factors. Correlations of antioxidant tests and fruit composition assays indicate that pH, SSC, and titratable acidity cannot be used as simple predictors of total phenolic, total anthocyanin, or FRAP values (data not shown). Of the total antioxidant tests used, total phenolics appears to be the best quick test, as it is the easiest of the assays, showed the least change among years, and correlated highly with FRAP.

ACKNOWLEDGEMENTS

The assistance of Jungmin Lee, Mary Peterson, Ted Mackey, Chris Rennaker, Sheila Magby, and Brian Yorgey is gratefully acknowledged. This work was partially funded through the Center for Agroforestry, University of Missouri under cooperative agreements with the USDA-ARS Dale Bumpers Small Farm Research Center, Booneville, AR. We thank the USDA-Agricultural Research Service (ARS) CRIS numbers 5358-21000-041-00D, 5358-21000-037-00D and Northwest Center for Small Fruits Research for funding as well as for their technical assistance with this project. This publication was also made possible by Grant Number P50AT006273 from the National Center for Complementary and Alternative Medicines (NCCAM), the Office of Dietary Supplements (ODS), and the National Cancer Institute (NCI), and with funds from the USDA Crop Germplasm Committee, Small Fruits. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NCCAM, ODS, NCI, USDA, or the National Institutes of Health. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the USDA.

Literature Cited

  1. Benzie IFF, Strain JJ. Ferric reducing/antioxidant power assay: direct measure of total antioxidant activity of biological fluids and modified version for simultaneous measurement of total antioxidant power and ascorbic acid concentration. Methods in Enzymology. 1999;299:15–27. doi: 10.1016/s0076-6879(99)99005-5. [DOI] [PubMed] [Google Scholar]
  2. Charlebois D, Byers PL, Finn CE, Thomas AL. Elderberry: botany, horticulture, potential. In: Janick J, editor. Horticulture Reviews. Vol. 37. Wiley-Blackwell; New Jersey: 2010. pp. 213–280. [Google Scholar]
  3. Finn CE, Thomas AL, Byers PL, Serçe S. Evaluation of American (Sambucus canadensis) and European (S. nigra) elderberry genotypes grown in diverse environments and implications for cultivar development. HortScience. 2008;43:1385–1391. [Google Scholar]
  4. Lee J, Finn CE. Anthocyanins and other polyphenolics in American elderberry (Sambucus canadensis) and European elderberry (S. nigra) cultivars. J. Sci. Food Agr. 2007;87:2665–2675. doi: 10.1002/jsfa.3029. [DOI] [PubMed] [Google Scholar]
  5. Mohebalian PM, Cernusca MM, Aguilar FF. Discovering niche markets for elderberry juice in the United States. HortTechnol. 2012;22:556–566. [Google Scholar]
  6. Nakatani N, Kikuzak H, Hikida J, Ohba M, Inami O, Tamura I. Acylated anthocyanins from fruits of Sambucus canadensis. Phytochemistry. 1995;3:755–757. doi: 10.1016/0031-9422(94)00700-4. [DOI] [PubMed] [Google Scholar]
  7. Özgen M, Scheerens JC, Reese RN, Miller RA. Total phenolics, anthocyanin contents and antioxidant capacity of selected elderberry (Sambucus canadensis L.) accessions. Pharmacogn. Mag. 2010;6:198–203. doi: 10.4103/0973-1296.66936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Roschek B, Jr., Fink RC, McMichael MD, Li D, Alberte RS. Elderberry flavonoids bind to prevent H1N1 infection in vitro. Phytochemistry. 2009;70:1255–1261. doi: 10.1016/j.phytochem.2009.06.003. [DOI] [PubMed] [Google Scholar]
  9. Thomas AL, Byers P. Multi-locational elderberry cultivar and management study. Proc. Missouri Small Fruit Conf.; Springfield, MO: Southwest Missouri State Univ.; 2000. pp. 37–40. [Google Scholar]
  10. Thomas AL, Perkins-Veazie P, Byers PL, Finn CE, Lee J. A comparison of fruit characteristics among diverse elderberry genotypes grown in Missouri and Oregon. J. Berry Res. 2013;3:159–168. doi: 10.3233/JBR-130054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Zakay-Rones Z, Varsano N, Zlotnik M, Manor O, Regev L, Schlesinger M, Mumcuoglu M. Inhibition of several strains of influenza virus in vitro and reduction of symptoms by an elderberry extract (Sambucus nigra L.) during an outbreak of influenza B Panama. J. Altern. Complementary Med. 1995;1:361–369. doi: 10.1089/acm.1995.1.361. [DOI] [PubMed] [Google Scholar]

RESOURCES