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Organic Acids, Free Sugars, and Volatile Flavor Compounds by Type of Jerusalem Artichoke

돼지감자의 품종별 유기산, 유리당 및 휘발성 향기성분

  • Jung, Bok-Mi (Division of Food and Nutrition, Chonnam National University / Human Ecology Research Institute) ;
  • Shin, Tai-Sun (Division of Food and Nutrition, Chonnam National University / Human Ecology Research Institute)
  • 정복미 (전남대학교 식품영양과학부/ 생활과학연구소) ;
  • 신태선 (전남대학교 식품영양과학부/ 생활과학연구소)
  • Received : 2017.04.18
  • Accepted : 2017.06.19
  • Published : 2017.07.31

Abstract

This study analyzed contents of organic acids, free sugars, and volatile flavor compounds by type of Jerusalem artichoke (Helianthus tuberosus L.). Organic acids in dried Jerusalem artichoke were mainly composed of malic acid, citric acid, and succinic acid. Sucrose, fructose, and glucose were the major sugar components of dried Jerusalem artichoke. Free sugars were more abundant in the white colored sample than in the purple colored sample. In contrast, purple colored sample contained more organic acids than the white colored one. Volatile compounds in Jerusalem artichoke were investigated using the solid-phase micro-extraction method of gas chromatography/mass spectrometry. A total of 117 volatile compounds were identified in Jerusalem artichoke, and chemical classification was as follows: 5 acids, 13 alcohols, 19 aldehydes, 12 hydrocarbons, 15 ketones, 8 miscellaneous, 27 pyrazines, and 18 terpenes in all samples. Terpene was the most abundant in Jerusalem artichoke, and ${\beta}$-bisabolene was the main component in terpenes. The second most common compound was aldehyde, and hexanal was the highest. Pyrazines were the most abundant in the roasted samples, and 2,5-dimethyl-3-ethylpyrazine was present at the highest level, followed by 2,5-dimethylpyrazine. Compared with purple samples, main compounds contained in white samples were aldehydes and hydrocarbons, whereas the major compounds in purple samples were terpenes and alcohols.

돼지감자의 품종별 유기산, 유리당 함량 및 휘발성 향기성분을 측정한 결과는 다음과 같다. 돼지감자에 함유된 유기산은 citric acid, malic acid, succinic acid였으며, malic acid의 함량이 가장 높았고 다음으로 citric acid로 나타났다. 총유기산 함량은 흰색이 2,065 mg/100 g, 자색은 2,482 mg/100 g으로 자색 돼지감자의 함량이 유의적으로(P<0.05) 높았다. 유리당은 sucrose, fructose, glucose로 나타났으며, sucrose의 함량이 가장 높았고 총유리당 함량은 흰색이 24.95 g/100 g, 자색이 11.57 g/100 g으로 나타나 흰색 돼지감자의 총유리당 함량이 유의적으로(P<0.05) 높게 나타났다. 휘발성 향기성분에서 돼지감자는 품종별, 처리방법과는 관계없이 acid류 5종, alcohol류 13종, aldehyde류 19종, hydrocarbon류 12종, ketone류 15종, 기타 8종, pyrazine류는 27종, terpene류는 18종이었으며, 총 117개의 휘발성 성분이 확인되었다. 돼지감자에는 terpene류가 가장 많았으며, terpene류 중에서는 ${\beta}$-bisabolene이 주된 성분이었다. 두 번째로 많은 화합물은 aldehyde류였으며, hexanal이 가장 높게 나타났다. 처리방법에 따른 차이로 볶은 시료에서는 pyrazine류가 대부분을 차지하였으며, 2,5-dimethyl-3-ethylpyrazine이 가장 높았고 다음으로 2,5-dimethylpyrazine으로 나타났다. 자색시료보다 흰색시료에 함량이 높은 화합물은 aldehyde류, hydrocarbone류였으며, 흰색시료보다 자색시료에 많은 화합물은 terpene류와 alcohol류로 나타났다.

Keywords

References

  1. Lim KB, Lee HJ. 1989. Seed dormancy of Jerusalem artichoke (Helianthus tuberosus L.) and seed treatment for germination induction. Korean J Crop Sci 34: 370-377.
  2. Cieslik E, Gebusia A, Florkiewicz A, Mickowska B. 2011. The content of protein and of amino acids in Jerusalem artichoke tubers (Helianthus tuberosus L.) of red variety Rote Zonenkugel. Acta Sci Pol Technol Aliment 10: 433-441.
  3. Shin SH, Kwon SJ, Jo HJ, Go D, Han J. 2012. Extraction and analysis of inulin from Jerusalem artichoke. Food Science and Industry 45(4): 50-58.
  4. Kim SH. 2014. Jerusalem artichoke and inulin. J Korean Diabetes 15: 227-231. https://doi.org/10.4093/jkd.2014.15.4.227
  5. Jhon DY, Kim MH. 1988. Studies inulase from Jerusalem artichoke. J Korean Soc Food Sci Nutr 17: 205-210.
  6. Chae EM, Chol EH. 1991. Optimization for alcohol fermentation by Kluyveromyces marxianus using Jerusalem artichoke powder. Kor J Appl Microbiol Biotechnol 19: 265-271.
  7. Rosengard BR, Cochrane DE. 1983. Complement-mediated cytolysis: A quick, simple method for determining levels of immunoglobulin E bound to mast cells. J Histochem Cytochem 31: 441-444. https://doi.org/10.1177/31.3.6827080
  8. Jeong HJ, Kim JS, Sa YJ, Kim MO, Yang J, Kim MJ. 2011. Antioxidant activity and ${\alpha}$-glucosidase inhibitory effect of Jerusalem artichoke (Helianthus tuberosus) methanol extract by heat treatment conditions. Korean J Med Crop Sci 19: 257-263. https://doi.org/10.7783/KJMCS.2011.19.4.257
  9. Kang SI, Han JI, Kim KY, Oh SJ, Kim SI. 1993. Changes in soluble neutral carbohydrates composition of jerusalem artichoke (Helianthus tuberosus L.) tubers according to harvest date and storage temperature. J Korean Agric Chem Soc 36: 304-309.
  10. Kim YS, Lee SJ, Hwang JW, Kim EH, Park PJ, Jeon BT. 2011. Antioxidant activity and protective effects of extracts from Helianthus tuberosus L. leaves on t-BHP induced oxidative stress in chang cells. J Korean Soc Food Sci Nutr 40: 1525-1531. https://doi.org/10.3746/jkfn.2011.40.11.1525
  11. Kim JW, Kim JK, Song IS, Kwon ES, Youn KS. 2013. Comparison of antioxidant and physiological properties of Jerusalem artichoke leaves with different extraction processes. J Korean Soc Food Sci Nutr 42: 68-75. https://doi.org/10.3746/jkfn.2013.42.1.068
  12. Park HS. 2010. Quality characteristics of Sulgidduk by the addition of Jerusalem artichoke powder. Korean J Culinary Res 16: 259-267.
  13. Kim GC, Kim HS, Jo IH, Kim JS, Kim KM, Jang YE. 2013. Qualitative characteristics and antioxidant activities of Buchimgaru supplemented with Jerusalem artichoke powder. J Korean Soc Food Sci Nutr 42: 1065-1070. https://doi.org/10.3746/jkfn.2013.42.7.1065
  14. Food Journal. http://www.foodnews.co.kr/news/articleView.html?idxno=57265 (accessed Dec 2015).
  15. Shin TS, Xue Z, Do YW, Jeong SI, Woo HC, Kim NG. 2011. Chemical properties of sea tangle (Saccharina japonica) cultured in the different depths of seawater. Clean Technol 17: 395-405.
  16. Lisinska G, Leszczynski W. 1989. Potato science and technology. Elsevier Science Published Ltd., Barking, UK. p 35-36,151-153.
  17. Bushway RJ, Bureau JL, Mcgann DF. 1984. Determinations of organic acids in potatoes by high performance liquid chromatography. J Food Sci 49: 76-77. https://doi.org/10.1111/j.1365-2621.1984.tb13673.x
  18. Wichrowska D, Rogozińska I, Pawelzik E. 2009. Concentrations of some organic acids in potato tubers depending on weed control method, cultivar and storage conditions. Polish J Environ Stud 18: 487-491.
  19. Jarvis MC, Dalziel J, Duncan HJ. 1974. Variations in free sugars and lipids in different potato varieties during lowtemperature storage. J Sci Food Agric 25: 1405-1409. https://doi.org/10.1002/jsfa.2740251108
  20. Lindner K, Haase NU, Roman M, Seemüller E. 2011. Impact of stolbur phytoplasmas on potato tuber texture and sugar content of selected potato cultivars. Potato Res 54: 267-282. https://doi.org/10.1007/s11540-011-9192-3
  21. Kumar D, Singh BP, Kumar P. 2004. An overview of the factors affecting sugar content of potatoes. Ann Appl Biol 145: 247-256. https://doi.org/10.1111/j.1744-7348.2004.tb00380.x
  22. MacLeod AJ, Pieris NM, de Troconis NG. 1982. Aroma volatiles of Cynara scolymus and Helianthus tuberosus. Phytochem 21: 1647-16511. https://doi.org/10.1016/S0031-9422(82)85033-4
  23. Kato H, Ohta T, Tsugita T, Hosaka Y. 1983. Effect of parboiling on texture and flavor components of cooked rice. J Agric Food Chem 31: 818-823. https://doi.org/10.1021/jf00118a035
  24. Mehinagic E, Royer G, Symoneaux R, Jourjon F, Prost C. 2006. Characterization of odor-active volatiles in apples: influence of cultivars and maturity stage. J Agric Food Chem 54: 2678-2687. https://doi.org/10.1021/jf052288n
  25. Ulrich D, Hoberg E, Neugebauer W, Tiemann H, Darsow U. 2000. Investigation of the boiled potato flavor by human sensory and instrumental methods. Am J Potato Res 77: 111-117. https://doi.org/10.1007/BF02853738
  26. Maga JA. 1994. Potato flavor. Food Rev Int 10: 1-48. https://doi.org/10.1080/87559129409540984
  27. Galliard T. 1973. Lipids of potato tubers. I. Lipid and fatty acid composition of tubers from different varieties of potato. J Sci Food Agric 24: 617-622. https://doi.org/10.1002/jsfa.2740240515
  28. Josephson DB, Lindsay RC. 1987. c4-Heptenal: An influential volatile compound in boiled potato flavor. J Food Sci 52: 328-331. https://doi.org/10.1111/j.1365-2621.1987.tb06605.x
  29. Petersen MA, Poll L, Larsen LM. 1998. Comparison of volatiles in raw and boiled potatoes using a mild extraction technique combined with GC odour profiling and GC-MS.
  30. Poisson L, Schieberle P. 2008. Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis. J Agric Food Chem 56: 5813-5819. https://doi.org/10.1021/jf800382m
  31. Botelho G, Mendes-Faia A, Climaco MC. 2008. Differences in odor-active compounds of trincadeira wines obtained from five different clones. J Agric Food Chem 56: 7393-7398. https://doi.org/10.1021/jf8011008
  32. van Loon WAM, Linssen JPH, Legger A, Posthumus MA, Voragen AGJ. 2005. Identification and olfactometry of French fries flavour extracted at mouth conditions. Food Chem 90: 417-425. https://doi.org/10.1016/j.foodchem.2004.05.005
  33. Soria AC, González M, de Lorenzo C, Martinez-Castro I, Sanz J. 2004. Characterization of artisanal honeys from Madrid (Central Spain) on the basis of their melissopalynological, physicochemical and volatile composition data. Food Chem 85: 121-130. https://doi.org/10.1016/j.foodchem.2003.06.012
  34. Wanakhachornkrai P, Lertsiri S. 2003. Comparison of determination method for volatile compounds in Thai soy sauce. Food Chem 83: 619-629. https://doi.org/10.1016/S0308-8146(03)00256-5
  35. Nursten HE, Sheen MR. 1974. Volatile flavor components of cooked potato. J Sci Food Agric 25: 643-663. https://doi.org/10.1002/jsfa.2740250607
  36. Gomez E, Ledbetter CA, Hartsell PL. 1993. Volatile compounds in apricot, plum, and their interspecific hybrids. J Agric Food Chem 41: 1669-1676. https://doi.org/10.1021/jf00034a029
  37. Umano K, Hagi Y, Nakahara K, Shoji A, Shibamoto T. 2000. Volatile chemicals identified in extracts from leaves of Japanese mugwort (Artemisia princeps Pamp.). J Agric Food Chem 48: 3463-3469. https://doi.org/10.1021/jf0001738
  38. Lamikanra O, Richard OA. 2002. Effect of storage on some volatile aroma compounds in fresh-cut cantaloupe melon. J Agric Food Chem 50: 4043-4047. https://doi.org/10.1021/jf011470v
  39. Joulain D, Casazza A, Laurent R, Portier D, Guillamon N, Pandya R, Le M, Viljoen A. 2004. Volatile flavor constituents of fruits from Southern Africa: Mobola plum (Parinari curatellifolia). J Agric Food Chem 52: 2322-2325. https://doi.org/10.1021/jf030702i
  40. Chen JL, Wu JH, Wang Q, Deng H, Hu XS. 2006. Changes in the volatile compounds and chemical and physical properties of Kuerle fragrant pear (Pyrus serotina Reld) during storage. J Agric Food Chem 54: 8842-8847. https://doi.org/10.1021/jf061089g
  41. Budavari S. O'Neil MJ, Smith A, Heckelman PE, Kinneary JF. 1996. The Merck Index: An encyclopedia of chemicals, drugs, and biologicals. 12th ed. Merck Research Laboratories, Merck & Co., Inc., Whitehouse Station, NJ, USA. p1062.
  42. Park NY, Jeong YJ, Kwon JH. 2007. Changes in flavor compounds of Polygonatum odoratum root during roasting. Korena J Food Sci Technol 39: 99-103.
  43. Buttery RG, Guadagni DG, Ling LC. 1973. Volatile components of baked potatoes. J Sci Food Agric 24: 1125-1131. https://doi.org/10.1002/jsfa.2740240916
  44. Coleman EC, Ho CT, Chang SS. 1981. Isolation and identification of volatile compounds from baked potatoes. J Agric Food Chem 29: 42-48. https://doi.org/10.1021/jf00103a012
  45. Josephson DB, Lindsay RC. 1987. c4-Heptenal: an influential volatile compound in boiled potato flavor. J Food Sci 52: 328-331. https://doi.org/10.1111/j.1365-2621.1987.tb06605.x
  46. Kim SS. 1996. Effects of maturing barley kernels on flavor characteristics during roasting. PhD Dissertation. Chung-Ang University, Seoul, Korea.
  47. Mega JA, Sizer CE. 1973. Pyrazines in foods. Review. J Agric Food Chem 21: 22-30. https://doi.org/10.1021/jf60185a006
  48. Ziegleder G. 1982. Gaschromatographische rostgradbestimmung von kakao uber unethylierte pyrazine. Dtsch Lebensm-Rundsch 78: 77-81.
  49. van den Dool H, Kratz PD. 1963. A generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography. J Chromatogr 11: 463-471. https://doi.org/10.1016/S0021-9673(01)80947-X
  50. Mass Spectrometry Data Centre. 1974. Eight peak index of mass spectra. 2nd ed. Mass Spectrometry Data Centre, Aldermaston, UK.
  51. Jennings W, Shibamoto T. 1980. Qualitative analysis of flavor and fragrance volatiles by glass capillary gas chromatography. Academic Press, New York, NY, USA.
  52. Sadtler Research Laboratories. 1985. The Sadtler standard gas chromatography retention index library (Vol 1-4). Division of Bio-Rad Laboratories, Inc., Philadelphia, PA, USA.