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2013 | 12 | 2 |

Tytuł artykułu

Changes in amino acids content in tubers of jerusalem artichoke (Helianthus tuberosus L.) cultivars during storage

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The objective of the three-year study was to determine the influence of postharvest storage on essential and nonessential amino acids content in tubers of different cultivars of Jerusalem artichoke (Helianthus tuberosus L.) – ‘Rubik’, ‘Albik’ and ‘Sauliai’. The experiment was performed in 2007–2009. The plants were grown in the experimental field of Lithuanian University of Agriculture in Kaunas (from 2011 August – Aleksandras Stulginskis university). The Jerusalem artichoke tubers were stored for 20 weeks at the temperature of 2°C (± 0.5°C) and RH 90–95 % in polypropylene (PP) perforated bags, capacity of 10 kg, in 4 replicates. Amino acids contents were determined immediately after harvest and during storage of the tubers in every 4 weeks by the method of ion-exchange chromatography and then detected photometrically. The data obtained were statistically analyzed with two-factor Anova (STATISTICA software). Standard deviation and the least significant difference at the 95% probability level were calculated with Fisher’s LSD test. Data presented in tables are mean values of the three years of the experiment. The results obtained showed that directly after harvest and during the storage the dominating amino acid in tubers of all cultivars was of essential amino acids – arginine, and of nonessential – asparagine, glutamine and alanine. Tubers of cv. ‘Sauliai’ after 20 week storage accumulated the highest amount of essential amino acids – treonine, valine, isoleucine, leucine, phenylalanine and nonessential – serine, glycine, alanine, tyrosine. Significant correlations between contents of some amino acids in the tubers were found.
PL
Celem trzyletnich badań było określenie wpływu przechowywania pozbiorczego na zawartość egzogennych i endogennych aminokwasów w bulwach topinamburu (Helianthus tuberosus L.) trzech odmian uprawnych: ‘Rubik’, ‘Albik’ i ‘Sauliai’. Bulwy przechowywano przez okres do 20 tygodni w temperaturze 2 C (± 0,5 C) oraz warunkach wilgotności względnej (90–95%). Wyniki wskazują, że bezpośrednio po zbiorze oraz podczas przechowywania dominującym aminokwasem spośród amainokwasów egzogennych u wszystkich odmian była arginina, a spośród aminokwasów endogennych asparagina, glutamina i alanina. Bulwy odmiany ‘Sauliai’ po 20 tygodniach przechowywania akumulowały najwięcej egzogennych aminokwasów – treoniny, waliny, izoleucyny, leucyny, fenyloalaniny i endogennych – seryny, glicyny, alaniny i tyrozyny. Stwierdzono silne korelacje między zawartościami niektórych aminokwasów w bulwach.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

12

Numer

2

Opis fizyczny

p.97-105,fig.,ref.

Twórcy

  • Department of Horticulture, Faculty of Agronomy, Aleksandras Stulginskis University, Studentu 11, Akademija, LT – 53356 Kaunas, Lithuania
autor
  • Department of Horticulture, Faculty of Agronomy, Aleksandras Stulginskis University, Studentu 11, Akademija, LT – 53356 Kaunas, Lithuania
autor
  • Warsaw University of Life Sciences – SGGW, Warsaw, Poland
autor
  • University of Life Sciences in Lublin, Lublin, Poland
  • Department of Horticulture, Faculty of Agronomy, Aleksandras Stulginskis University, Studentu 11, Akademija, LT – 53356 Kaunas, Lithuania
  • Department of Horticulture, Faculty of Agronomy, Aleksandras Stulginskis University, Studentu 11, Akademija, LT – 53356 Kaunas, Lithuania

Bibliografia

  • Bagni N., Malucelli B., Torrigiani P., 1980. Polyamines storame substances and abscisic-acid-like inhibitors during dormancy and very early activation of Helianthus tuberosus tuber tissues. Physiol. Plant. 49, 341–345.
  • Ben Chekroun M., Amzile J., Mokhtari A., El Haloui N.E., Prevost J., Fontanillas R., 1996. Comparison of fructose production by 37 cultivars of Jerusalem artichoke (Helianthus tuberosus L.). New Zeal. J. Crop Hort. Sci. 24, 115–120.
  • Brierley E.R., Bonner P.L.R., Cobb A.H., 1996. Factors influencing the free amino acid content of potato (Solanum tuberosum L.) tubers during prolonged storage. J. Sci. Food Agric. 70, 515– 525.
  • Ciborowska H., Rudnicka A., 2007. Dietetyka. ĩywienie zdrowego i chorego czáowieka. PZWL Warszawa.
  • Cieślik E., Kopeć A., Praznik W., 2005. Healthy properties of Jerusalem artichoke flour (Helianthus tuberoses L.). htpp://www.ejpau.media.pl/volume8/issue2/art-37.html.
  • Danilčenko H., Jariene E., Aleknaviciene P., Gajewski M., 2008. Quality of Jerusalem artichoke (Helianthus tuberosus L.) tubers in relation to storage conditions. Not. Bot. Horti Agrobot. Cluj. 36 (2), 23–27.
  • Danilčenko H., Jarienơ E., Taraseviþienơ Ž., Aleknaviþienơ P., Kulaitienơ J., Kita A., Gajewski M., Bliznikas S., Lukšienơ Ž., 2009. Quality and safety aspects of some new generation food products in Lithuania. Food Quality and Safety. Wyd. UP Wrocáaw, 55–64.
  • Deuschle K., Funck D., Hellmann H., Däschner K., Binder S., Frommer W.B., 2001. A nuclear gene encoding mitochondrial Delta-pyrroline-5-carboxylate dehydrogenase and its potential role in protection from proline toxicity. Plant J. 27, 345–356.
  • Dougall D.K., 1966. Biosynthesis of protein amino acids in plant tissue culture II further isotope competition experiments using protein amino acids. Plant Physiol. 41, 1411–1415.
  • Dorrell D.G., Chubey B.B., 1977. Irrigation, fertilizer, harvest dates, and storage effects on the reducing sugar and fructose concentrations of Jerusalem artichoke tubers. Canad. J. Plant Sci. 57, 591.
  • Hamilton E.W., Heckathorn S.A., 2001. Mitochondrial adaptations to NaCl complex I is protected by anti-oxidants and small heat shock proteins, whereas complex II is protected by proline and betaine. Plant Physiol. 126, 1266–1274
  • Kaldy M.S., Johnston A., Wilson D.B., 1980. Nutritive value of Indian Bread-root, squaw-root, and Jerusalem Artichoke. Econ. Bot. 34 (4), 352–357.
  • Kiyosue T., Yoshiba Y., Yamaguchi-Shinozaki K., Shinozaki K., 1996. A nuclear gene encoding mitochondrial proline dehydrogenase, an enzyme involved in proline metabolism, is upregulated by proline but downregulated by dehydration in Arabidopsis. Plant Cell 8, 1323–1335.
  • Maggio A., Miyazaki S., Veronese P., Fujita T., Ibeas J.I., Damsz B., Narasimhan M.L., Hasegawa P.M., Joly R.J., Bressan R.A., 2002. Does proline accumulation play an active role in stress-induced growth reduction? Plant J. 31, 699–712.
  • Miller G., Honig A., Stein H., Suzuki N., Mittler R., Zilberstein A., 2009. Unraveling delta1- pyrroline-5-carboxylate-proline cycle in plants by uncoupled expression of proline oxidation enzymes. J. Biol. Chem. 284, 26482–26492.
  • Strizhov N., Abrahám E., Okrész L., Blickling S., Zilberstein A., Schell J., Koncz C., Szabados L., 1997. Differential expression of two P5CS genes controlling proline accumulation during salt-stress requires ABA and is regulated by ABA1, ABI1 and AXR2 in Arabidopsis. Plant J. 12, 557–569.
  • Serafini-Fracassini D., Mossetti U., 1985. Free and bound polyamines in different physiological stages of Helianthus tuberosus tuber. W: Recent Progression in Polyamine Research L. Selmeci, Brosnan M., Seiler N. (red.). Akademiai Kiadò, Budapest, 551–560.
  • Technical regulation of amino acids amount determination in feed. Normative act compendium, 2003. Kaunas, 66–77 (in Lithuanian).
  • Verbruggen N., Hua X.J., May M., Van Montagu M., 1996. Environmental and developmental signals modulate proline homeostasis: evidence for a negative transcriptional regulator. Proc. Natl. Acad. Sci. U.S.A. 93, 8787–8791.
  • Xue X., Liu A., Hua X., 2009. Proline accumulation and transcriptional regulation of proline biosynthesis and degradation in Brassica napus. BMB Rep. 42, 28–34

Typ dokumentu

Bibliografia

Identyfikatory

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