REVIEW PAPER
Topinambur – new possibilities for use in a supplementation diet
 
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1
Institute of Rural Health, Lublin, Poland
2
Medical University of Lublin, Poland
3
University of Life Sciences, Lublin, Poland
 
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ABSTRACT:
Jerusalem artichoke (Helianthus tuberosus Linne) is a tuberous perennial plant of the Asteraceae family, which originates from North America, and is also known as wild sunflower or topinambur (TPB). It is characterized by good tolerance to frost, drought and poor soil, strong resistance to pests and plant diseases. For ages it was cultivated due to being both an edible tuber and having healing properties. In folk medicine, TPB leaves are used for the treatment of bone fractures and pain. TPB tubers are rich in sugar and have therefore been used for the production of functional food ingredients, such as inulin. Moreover, TPB is one of the potential crops for bioenergy production, such as bioethanol, biobuthanol and biodiesel, and chemicals (lactic acid, butyric acid). A number of bioactive compounds from the above ground parts of this plant have been isolated which have demonstrating antifungal, antioxidant and anticancer activities. In recent years, a number of animal experiments have been carried out to assess the health properties of TPB. Obtained results show that TPB possess a wide spectrum of medical applications, e.g. reduction in the levels of plasma glucose, total cholesterol and triglyceride. Interestingly, TPB has been shown to be a valuable alternative source of prebiotic compounds. This review article presents recent scientific reports on the chemical and biological properties of TPB and its potential use as a prebiotic diet supplement.
CORRESPONDING AUTHOR:
Aleksandra Szewczyk   
Institute of Rural Health, Jaczewskiego 2, 20-090, Lublin, Poland
 
REFERENCES (46):
1. Yaeghoobi-Khanghahi F, Kazemi-Tabar SK, Gholipour A, Soorni J. GC-MS analysis of the methanolic extract of Jerusalem artichoke (Helianthus tuberosus) tubers. Int J Biosci. 2014; 5: 156–161.
2. De Santis D, Frangipane MT. Evaluation of chemical composition and sensory profile in Jerusalem artichoke (Helianthus tuberosus L) tubers: The effect of clones and cooking conditions. Int J Gastro Food Sci. 2018; 11: 25–30.
3. Yang L, He QS. Corscadden K, Udenigwe CC. The prospects of Jerusalem artichoke in functional food ingredients and bioenergy production. Biotechnol Rep. 2015; 5: 77–88.
4. Taha HS, El-Kawy AMA, Fathalla EK. A new approach for achievement of inulin accumulation in suspension cultures of Jerusalem artichoke (Helianthus tuberosus) using biotic elicitors. J Genet Eng Biotechnol. 2012; 10: 33–38.
5. Rosati A. Coltivate il topinambur, il sapore dei suoi tuberi ricorda quello del carciofo. Vita Camp. 2010; 10: 23–25.
6. Negro MJ, Ballesteros I, Manzanares P, Oliva JM, Sáez F, Ballesteros M. Inulin containing biomass for ethanol production: Carbohydrate extraction and ethanol fermentation. Appl Biochem Biotechnol. 2006; 132: 922–932.
7. Kaldy MS, Johnston A, Wilson DB. Nutritive value of Indian bread-root, squaw-root, and Jerusalem artichoke. Econ Bot. 1980; 34: 352–357.
8. De Leenheer L. Production and use of inulin: industrial reality with a promising future. In: Van Bekkum H, Roper H, Voragen F (eds) Carbohydrates as organic raw materials III. Wiley-VCH Verlag GmbH, Weinheim, 1996; 67–92.
9. Maicaurkaew S, Jogloy S, Hamaker BR, Ningsanond S. Fructan:fructan 1-fructosyltransferase and inulin hydrolase activities relating to inulin and soluble sugars in Jerusalem artichoke (Helianthus tuberosus Linn.) tubers during storage. J Food Sci Technol. 2017; 54(3): 698–706.
10. Saulnier DM, Ringel Y, Heyman MB, Foster JA, Bercik P, Shulman RJ, et al. The intestinal microbiome, probiotics and prebiotics in neurogastroenterology. Gut Microbes. 2013; 4(1): 17–27.
11. Kareb O, Aïder M. Whey and Its Derivatives for Probiotics, Prebiotics, Synbiotics, and Functional Foods: a Critical Review. Probiotics and Antimicrobial Proteins. 2018; 1–22.
12. Alles MS, Hautvast JG, Nagengast FM, Hartemink R, Van Laere KM, Jansen JB. Fate of fructo-oligosaccharides in the human intestine. Brit J Nutr. 1996; 76: 211–221.
13. Rastall RA, Gibson GR, Gill HS, Guarner F, Klaenhammer TR, Pot B, Reid G, Rowland IR, Sanders ME. Modulation of the microbial ecology of the human colon by probiotics, prebiotics and synbiotics to enhance human health: an overview of enabling science and potential applications. FEMS Microbiol Ecol. 2005; 52: 145–152.
14. Vogt L, Meyer D, Pullens G, Faas M, Smelt M, Venema K, et al. Immunological properties of inulin-type fructans Crit Rev Food Sci Nutr. 2015; 55: 414–436.
15. Shanzhao J, Ling L, Zhaopu L, Xiaohua L, Hongbo S, Jiayao C. Characterization of marine Pseudomonas pp. antagonist towards three tuber-rotting fungi from Jerusalem artichoke, a new industrial crop. Ind Crops Prod. 2013; 43: 556–561.
16. Panchev I, Delchev N, Kovacheva D, Slavov A. Physicochemical characteristics of inulins obtained from Jerusalem artichoke (Helianthus tuberosus L.). Eur Food Res Technol. 2011; 233: 889–896.
17. Praznik W, Cieslik E, Filipiak-Florkiewicz A. Soluble dietary fibers in Jerusalem artichoke powders: composition and application in bread.Nahrung. 2002; 46: 151–157.
18. Kim S, Kim CH. Evaluation of whole Jerusalem artichoke (Helianthus tuberosus L.) for consolidated bioprocessing ethanol production. Renew Energy 2014; 65: 83–91.
19. Pan L, Sinden MR, Kennedy AH, Chai H, Watson LE, Graham TL, Kinghorn AD. Bioactive constituents of Helianthus tuberosus (Jerusalem artichoke), Phytochem Lett. 2009; 2: 15–18.
20. Yuan XY, Gao MZ, Xiao HB, Tan CY, Du YG. Free radical scavenging activities and bioactive substances of Jerusalem artichoke (Helianthus tuberosus L.) leaves. J Food Chem. 2012; 133: 10–14.
21. Yuan XY, Cheng MC, Gao MZ, Zhuo RJ, Zhang LX, Xiao HB. Cytotoxic constituents from the leaves of Jerusalem artichoke (Helianthus tuberosus L.) and their structure–activity relationships. Phytochem Lett. 2013; 6: 21–25.
22. Liu HW, Liu ZP, Liu L, Zhao GM. Studies on the antifungal activities and chemical components of extracts from Helianthus tuberosus leaves. Nat Prod Res Dev. 2007; 19: 405–409.
23. Han R, Wang LH, Zhong QW, Sun K, Li Y. Study on antifungal activity of the extract from the leaves of Helianthus tuberosus. Mod Agric Sci Technol. 2010: 5.
24. Chen FJ, Long XH, Yu MN, Liu ZP, Liu L, Shao HB. Phenolics and antifungal activities analysis in industrial crop Jerusalem artichoke (Helianthus tuberosus L.) leaves. Indus Crops Prod. 2013; 47: 339–345.
25. Rubel IA, Pérez EE, Genovese DB, Manrique GD. In vitro prebiotic activity of inulin-rich carbohydrates extracted from Jerusalem artichoke (Helianthus tuberosus L.) tubers at different storage times by Lactobacillus paracasei. Food Res Int. 2014; 62: 59–65.
26. Hu JF, Qiu SY. Research process in ethanol production by the fermentation of Jerusalem artichoke. Liq.-Mark. Sci Technol. 2009; 182: 100–104.
27. Cheng Y, Zhou W, Gao CF, Lan K, Gao Y, Wu Q. Biodiesel production from Jerusalem artichoke (Helianthus Tuberosus L.) tuber by heterotrophic microalgae Chlorella protothecoides. J Chem Technol Biotechnol. 2009; 84:777–81.
28. Sung M, Seo YH, Han S, Han JI. Biodiesel production from yeast Cryptococcus sp. using Jerusalem artichoke. Bioresour Technol. 2014; 155: 77.
29. Sarchami T, Rehmann L. Optimizing enzymatic hydrolysis of inulin from Jerusalem artichoke tubers for fermentative butanol production, Biomass Bioenergy. 2014; 69: 175–182.
30. Chen L, Xin C, Deng P, Ren J, Liang H, Bai F. Butanol production from hydrolysate of Jerusalem artichoke juice by Clostridium acetobutylicum L7. Shengwu Gongcheng Xuebao/ Chin J Biotechnol. 2010; 26: 991e6.
31. Andersen AA, Greaves JE. d-lactic acid fermentation of Jerusalem artichokes. Ind Eng Chem. 1942; 24(12): 1522–6.
32. Ge X, Qian H, Zhang W. Improvement of l-lactic acid production from Jerusalem artichoke tubers by mixed culture of Aspergillus niger and Lactobacillus sp. Bioresour Technol. 2009; 100: 1872.
33. Wang L, Xue Z, Bo Z, Bo Y, Xu P, Ma Y. Jerusalem artichoke powder: a useful material in producing high-optical-purity l-lactate using an efficient sugar-utilizing thermophilic Bacillus coagulans strain. Bioresour Technol. 2013; 130: 174–80.
34. Huang J, Cai J, Wang J, Zhu X, Huang L, Yang ST, Xu Z. Efficient production of butyric acid from Jerusalem artichoke by immobilized Clostridium tyrobutyricum in a fibrous-bed bioreactor. Bioresour Technol. 2011; 102: 3923–6.
35. Liu XY, Chi Z, Liu GL, Wang F, Madzak C, Chi ZM. Inulin hydrolysis and citric acid production from inulin using the surface-engineered Yarrowia lipolytica displaying inulinase, Metab Eng. 2010; 12: 469–476.
36. Sridhar J, Eiteman MA. Influence of redox potential on product distribution in Clostridium thermosuccinogenes, Appl Biochem Biotechnol. 1999; 82: 91–101.
37. Wei W, Wu K, Qin Y, Xie Z, Zhu X. Intergeneric protoplast fusion between Kluyveromyces and Saccharomyces cerevisiae to produce sorbitol from Jerusalem artichokes, Biotechnol Lett. 2001; 23: 799–803.
38. Zaky EA. Physiological Response to Diets Fortified with Jerusalem Artichoke Tubers (Helianthus tuberosus L.) Powder by Diabetic Rats. Environ Sci. 2009; 5: 682–688.
39. Abdel-Hamid NM, Nazmy MH, Wahid A, Abdel-Moniem EM. Jerusalem artichoke attenuates experimental hepatic fibrosis via modulation of apoptotic signaling and fibrogenic activity. Biochemistry Biotechnol Res. 2015; 3: 43–50.
40. Wang PY, Kaneko T, Tsukada H, Nakano M, Nakajima T, Sato A. Time courses of hepatic injuries induced by chloroform and by carbon tetrachloride: comparison of biochemical and histopathological changes. Arch Toxicol. 1997; 71: 638–645.
41. Yang HJ, Kwon DY, Kim MJ, Kang S, Kim DS, Park S. Jerusalem artichoke and chungkookjang additively improve insulin secretion and sensitivity in diabetic rats. Nutr Metab (Lond) 2012; 9: 112.
42. Chang WC, Jia H, Aw W, Saito K, Hasegawa S, Kato H. Beneficial effects of soluble dietary Jerusalem artichoke (Helianthus tuberosus) in the prevention of the onset of type 2 diabetes and non-alcoholic fatty liver disease in high-fructose diet-fed rats. Br J Nutr. 2014; 112: 709–717.
43. Maicaurkaew S, Jogloy S, Hamaker BR, Ningsanond S. Fructan: fructan 1-fructosyltransferase and inulin hydrolase activities relating to inulin and soluble sugars in Jerusalem artichoke (Helianthus tuberosus Linn.) tubers during storage. J Food Sci Technol. 2017; 54(3): 698–706.
44. Samal L, Chaturvedi VB, Pattanaik AK. Effects of dietary supplementation with Jerusalem artichoke (Helianthus tuberosus L.) tubers on growth performance, nutrient digestibility, activity and composition of large intestinal microbiota in rats. J Anim Feed Sci. 2017; 26: 50–58.
45. Valdovska A, Jemeljanovs A, Pilmane M, Zitare I, Konosonoka IH, Lazdins M. Alternative for improving gut microbiota: use of Jerusalem artichoke and probiotics in diet of weaned piglets. Pol J Vet Sci. 2014; 17: 61–69.
46. Boonanuntanasarn S, Tiengtam N, Pitaksong T, Piromyou P, Teaumroong N. Effects of dietary inulin and Jerusalem artichoke (Helianthus tuberosus) on intestinal microbiota community and morphology of Nile tilapia (Oreochromis niloticus) fingerlings. Aquaculture Nut. 2018; 24: 712–722.
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