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Comparative analysis of the quality and health-promoting compounds of two-shaped fruits of wild Lycium ruthenicum Murr. from the Qinghai–Tibet Plateau

  • Yinyan QiEmail author
  • Chunyun Zhu
  • Jinfu Chen
  • Guiying Liu
  • Zhanwu Yang
  • Wusheng Chen
Original Article
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Abstract

Lycium ruthenicum Murr. is an econo-ecological tree species that abounds in the Qinghai–Tibet Plateau, which is located in the Chaka Salt Lake region of Qinghai Province, China. This study compared the phenotypes and main inclusions in two-shaped berries (flat peach and sphere types) at different developmental stages of L. ruthenicum Murr. to provide first-hand information for targeted breeding toward higher quality and stronger stress resistance of the fruit. Results showed the distinct advantage of the quality characters of flat peach-type fruits over the sphere-type with regard to the length of bearing shoot, internode, peduncle, single fruit weight, and 100-pod weight. In terms of inclusions, the anthocyanin contents in two-shaped fruits showed no significant difference at S5. Anthocyanin accumulated in the developing fruits, and the amount peaked at S4 and then gradually decreased. The expression profiles of the key genes in anthocyanin biosynthesis were correlated with anthocyanin accumulation during fruit development, and the high expressions of flavonoid 3′,5′-hydroxylase gene and dihydroflavonol 4-reductase gene were found to be the critical factors of specific delphinidin accumulation. Sphere-type mature fruits had considerable higher total polyphenol level than flat peach fruits, but the opposite result was observed for polysaccharides. The contents of Ca, Co, Cr, Cu, K, Li, Mn, P, Ti, V, and Al presented no considerable differences, whereas B, Mg, Na, Si, and Zn exhibited evident advantages in sphere-type fruits. α-Toc was the most abundant component in both fruits and no evident difference in its content was observed. The data on nutritional contents provide a theoretical basis for different breeding goals of L. ruthenicum and its further utilization as health food.

Keywords

Lycium ruthenicum Murr. Breed selection Fruit inclusion Differential analysis 

Abbreviations

CHS

Chalcone synthase gene

F3′5′H

Flavonoid 3′,5′-hydroxylase gene

F3H

Flavanone 3-hydroxylase gene

F3′H

Flavonoid 3′-hydroxylase gene

DFR

Dihydroflavonol 4-reductase gene

ANS

Anthocyanidin synthase gene

Notes

Acknowledgements

This study was funded by the Qinghai Province Natural Science Foundation of China (Grant no. 2014-ZJ-946Q), Qinghai Academy of Agricultural and Forestry Sciences Innovation Foundation (Grant no. 2014-NKY-01), Open Foundation of Key Laboratory of Qinghai Province for Plateau Crop Germplasm Innovation and Utilization (Grant no. 2014-03), and Qinghai Province Basic Research Project (Grant no. 2018-ZJ-713).

References

  1. Adachi N, Migita M, Ohta T, Higashi A, Matsuda I (1997) Depressed natural killer cell activity due to decreased natural killer cell population in a vitamin E-deficient patient with Shwachman syndrome: reversible natural killer cell abnormality by α-tocopherol supplementation. Eur J Pediatr 156(6):444–448CrossRefGoogle Scholar
  2. Altintas A, Kosar M, Kirimer N, Baser K, Demirci B (2006) Composition of the essential oils of Lycium barbarum, and L. ruthenicum fruits. Chem Nat Compd 42(1):24–25CrossRefGoogle Scholar
  3. Butelli E, Titta L, Giorgio M, Mock HP, Matros A, Peterek S, Schijlen E, Hall RD, Bovy AG, Luo J, Martin C (2008) Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors. Nat Biotechnol 26:1301–1308CrossRefGoogle Scholar
  4. Chen C, Shao Y, Li Y, Chen T (2014) Trace elements in Lycium Barbarum L. leaves by inductively coupled plasma mass spectrometry after microwave assisted digestion and multivariate analysis. Spectrosc Lett 48:775–780CrossRefGoogle Scholar
  5. Cirilli M, Bassi D, Ciacciulli A (2016) Sugars in peach fruit: a breeding perspective. Hortic Res 3:15067CrossRefGoogle Scholar
  6. Crisosto C, Costa G (2008) Preharvest factors affecting peach quality. In: Layne DR, Bassi D (eds) The peach: botany, production and uses. CAB International, Wallingford, pp 536–549CrossRefGoogle Scholar
  7. Danova K, Nikolova-Damianova B, Denev R, Dimitrov D (2012) Influence of vitamins on polyphenolic content, morphological development, and stress response in shoot cultures of Hypericum spp. Plant Cell Tissue Organ Culture 110(110):383–393CrossRefGoogle Scholar
  8. Grimm MOW, Stahlmann CP, Mett J, Haupenthal V, Zimmer V, Lehmann J, Hundsdӧrfer B, Endres K, Grimm H, Hartmann T (2015) Vitamin E: curse or benefit in Alzheimer’s disease? A systematic investigation of the impact of α-, γ- and δ-tocopherol on Aβ generation and degradation in neuroblastoma cells. J Nutr Health Aging 19:1–9CrossRefGoogle Scholar
  9. Katsumoto Y, Mizutani M, Fukui Y, Brugliera F, Holton T, Karan M, Nakamura N, Yonekura-Sakakibara K, Togami J, Pigeaire A, Tao GQ, Nehra NS, Lu CY, Dyson BK, Tsuda S, Ashikari T, Kusumi T, Mason JG, Tanaka Y (2007) Engineering of the rose flavonoid biosynthetic pathway successfully generated blue-hued flowers accumulating delphinidin. Plant Cell Physiol 48:1589–1600CrossRefGoogle Scholar
  10. Li J, Zhao H, Yuan H, Zhu C, Shi D (2006) Study on the pigment of Lycium ruthenicum Murr. Food Sci 27(10):146–151 (in Chinese) Google Scholar
  11. Li H, Liu H, Han Y, Wu X, Teng W, Liu G, Li W (2010) Identification of QTL underlying vitamin E contents in soybean seed among multiple environments. Theor Appl Genet 120(7):1405–1413CrossRefGoogle Scholar
  12. Liu L, Sun Y, Laura T, Liang X, Ye H, Zeng X (2009) Determination of polyphenolic content and antioxidant activity of kudingcha made from Ilex kudingcha, C.J. Tseng. Food Chemistry 112(1):35–41CrossRefGoogle Scholar
  13. Liu Ch, Li J, Meng F, Liang S, Deng R, Li Ch, Pong NH, Lau Ch, Cheng S, Ye J, Chen J, Yang ST, Yan H, Chen S, Chong B, Yang M (2010) Polysaccharides from the root of Angelica sinensis, promotes hematopoiesis and thrombopoiesis through the PI3K/AKT pathway. BMC Complement Altern Med 10(1):1–12CrossRefGoogle Scholar
  14. Lowe J, Marth J (2003) A genetic approach to mammalian glycan function. Annu Rev Biochem 72(1):643–691CrossRefGoogle Scholar
  15. Minas I, Tanou G, Molassiotyis A (2018) Environmental and orchard bases of peach fruit quality. Sci Hortic 235:307–322CrossRefGoogle Scholar
  16. Moyer R, Hummer K, Finn C, Frei B, Wrolstad R (2002) Anthocyanins, phenolics, and antioxidant capacity in diverse small fruits: vaccinium, rubus, and ribes. J Agric Food Chem 50(3):519–525CrossRefGoogle Scholar
  17. Peng Q, Song J, Lv X, Wang Z, Huang L, Du Y (2012) Structural characterization of an arabinogalactan-protein from the fruits of Lycium ruthenicum. J Agric Food Chem 60(37):9424–9429CrossRefGoogle Scholar
  18. Potterat O (2010) Goji (Lycium barbarum and L. chinense): phytochemistry, pharmacology and safety in the perspective of traditional uses and recent popularity. Planta Med 76(1):7–19CrossRefGoogle Scholar
  19. Pryor WA (2000) Vitamin E and heart disease: basic science to clinical intervention trials. Free Radic Biol Med 28(1):141–164CrossRefGoogle Scholar
  20. Qi Y, Lou Q, Li H, Yue J, Liu Y, Wang Y (2013) Anatomical and biochemical studies of bicolored flower development in Muscari latifolium. Protoplasma 250(6):1273–1281CrossRefGoogle Scholar
  21. Robards K, Prenzler P, Tucker G, Swatsitang P, Glover W (1999) Phenolic compounds and their role in oxidative processes in fruits. Food Chem 66(4):401–436CrossRefGoogle Scholar
  22. Serradilla M, Martín A, Ruiz-Moyano S, Hernández A, López-Corrales M, Córdoba M (2012) Physicochemical and sensorial characterisation of four sweet cherry cultivars grown in Jerte Valley (Spain). Food Chem 133(4):1551–1559CrossRefGoogle Scholar
  23. Szajdek A, Borowska EJ (2008) Bioactive compounds and health-promoting properties of berry fruits: a review. Plant Foods Hum Nutr 63(4):147–156CrossRefGoogle Scholar
  24. Tanaka Y, Brugliera F, Chandler S (2009) Recent progress of flower colour modification by biotechnology. Int J Mol Sci 10(12):5350–5369CrossRefGoogle Scholar
  25. Tokalıoğlu Ş (2012) Determination of trace elements in commonly consumed medicinal herbs by ICP-MS and multivariate analysis. Food Chem 134(4):2504–2508CrossRefGoogle Scholar
  26. Van Eenennaam A, Lincoln K, Durrett T, Valentin H, Shewmaker C, Thorne G, Jiang J, Baszis S, Levering C, Aasen E, Hao M, Stein J, Norris S, Last R (2003) Engineering vitamin E content: from Arabidopsis mutant to soy oil. Plant Cell 15(12):3007–3019CrossRefGoogle Scholar
  27. Xie Q, Liu Sh, Fan Y, Zhang X (2014) Development of a dispersive liquid–liquid microextraction method for the determination of α-tocopherol in pigmented wheat by high-performance liquid chromatography. Food Anal Methods 7(1):21–30CrossRefGoogle Scholar
  28. Zeng S, Wu M, Zou C, Liu X, Shen X, Hayward A, Liu C, Wang Y (2014) Comparative analysis of anthocyanin biosynthesis during fruit development in two Lycium species. Physiol Plant 150(4):505–516CrossRefGoogle Scholar
  29. Zheng J, Ding C, Wang L, Li G, Shi J, Li H, Wang H, Suo Y (2011) Anthocyanins composition and antioxidant activity of wild Lycium ruthenicum Murr. from Qinghai-Tibet Plateau. Food Chem 126(3):859–865CrossRefGoogle Scholar

Copyright information

© Franciszek Górski Institute of Plant Physiology, Polish Academy of Sciences, Kraków 2019

Authors and Affiliations

  • Yinyan Qi
    • 1
    • 2
    • 3
    • 4
    Email author
  • Chunyun Zhu
    • 1
    • 3
  • Jinfu Chen
    • 1
    • 3
  • Guiying Liu
    • 1
    • 3
  • Zhanwu Yang
    • 1
    • 3
  • Wusheng Chen
    • 1
    • 3
  1. 1.Qinghai Academy of Agriculture and Forestry SciencesQinghai UniversityXiningChina
  2. 2.State Key Laboratory of Plateau Ecology and AgricultureQinghai UniversityXiningChina
  3. 3.Qinghai Plateau Key Laboratory of Tree Genetics and BreedingXiningChina
  4. 4.State Key Laboratory Breeding BaseKey Laboratory of Qinghai Province for Plateau Crop Germplasm Innovation and UtilizationXiningChina

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