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2015 | 37 | 11 |

Tytuł artykułu

Biochemical characterization of the primary metabolism and antioxidant defense systems of acidic and acidless citrus genotypes during the major stages of fruit growth

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Fruits are consumed not just for their taste but also for their nutritional value. The major primary metabolites in fruit are sugars and acids, whose contents change during fruit growth and determine ultimate fruit quality. Fruits are also a source of antioxidant metabolites, which are important to human health due to their role in reducing risk of cancer and cardiovascular diseases. Antioxidants are equally important in the plant as they help fight against oxidative stress. Here, we investigated the consequences of changes in the primary metabolism in acidic and acidless citrus genotypes during the major stages of fruit growth on the expression of antioxidant enzymes and the markers of cellular oxidation (hydrogen peroxide, malondialdehyde) in acidless (Iaffaoui orange and sweet lemon) and acidic (Salustiana orange and Villafranca lemon) citrus fruits. Glucose and fructose were the major sugars in the acidless lemon. Sucrose was the major sugar in the acidic lemon. Oranges shared a balance of glucose, fructose, and sucrose. Malic and citric acid concentrations were higher in acidic lemons than acidless fruits. Acidic genotypes had higher hydrogen peroxide concentrations than acidless genotypes, whereas MDA concentrations were higher in oranges than in lemons. Specific activities of ascorbate peroxidase, catalase, superoxide dismutase, and dehydroascorbate reductase were on the whole higher in acidic than acidless fruits. Principal component analysis revealed between-genotype divergence in antioxidant system, giving three groups: acidic lemons, acidless lemons, and oranges.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

37

Numer

11

Opis fizyczny

Article: 228 [13 p.], fig.,ref.

Twórcy

autor
  • CNRS, UMR 6134 SPE, Laboratoire Biochimie and Biologie Moleculaire du Vegetal, 20250, Corte, France
autor
  • CNRS, UMR 6134 SPE, Laboratoire Biochimie and Biologie Moleculaire du Vegetal, 20250, Corte, France
  • UMR AGAP Corse, Station INRA, 20230, San Giuliano, France
  • CNRS, UMR 6134 SPE, Laboratoire Biochimie and Biologie Moleculaire du Vegetal, 20250, Corte, France
autor
  • Institut National de la Recherche Agronomique and Universite de Bordeaux, Unite Mixte de Recherche 1332, Biologie du Fruit et Pathologie, 33883, Villenave-d’Ornon, France
  • Metabolomics Platform–Functional Genomics Centre Bordeaux, INRA Bordeaux, 71 av Edouard Bourlaux, 33140, Villenave-d’Ornon, France
autor
  • UMR AGAP Corse, Station INRA, 20230, San Giuliano, France
autor
  • CNRS, UMR 6134 SPE, Laboratoire Biochimie and Biologie Moleculaire du Vegetal, 20250, Corte, France
autor
  • CNRS, UMR 6134 SPE, Laboratoire Biochimie and Biologie Moleculaire du Vegetal, 20250, Corte, France

Bibliografia

  • Ackermann J, Fischer M, Amado R (1992) Changes in sugars, acids, and amino acids during ripening and storage of apples (cv. Glockenapfel). J Agric Food Chem 40:1131–1134
  • Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126 Albertini M-V, Carcouet E, Pailly O et al (2006) Changes in organic acids and sugars during early stages of development of acidic and acidless citrus fruit. J Agric Food Chem 54:8335–8339
  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399
  • Aprile A, Federici C, Close TJ et al (2011) Expression of the H+-ATPase AHA10 proton pump is associated with citric acid accumulation in lemon juice sac cells. Funct Integr Genom 11:551–563
  • Asada K (1984) Chloroplasts-formation of active oxygen species. Methods Enzymol 105:422–429
  • Asada K (1999) The water–water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu Rev Plant Biol 50:601–639
  • Bain JM (1958) Morphological, anatomical, and physiological changes in the developing fruit of the Valencia orange, Citrus sinensis (L) Osbeck. Aust J Bot 6:1–24
  • Barkley NA, Roose ML, Krueger RR, Federici CT (2006) Assessing genetic diversity and population structure in a citrus germplasm collection utilizing simple sequence repeat markers (SSRs). Theor Appl Genet 112:1519–1531
  • Bermejo A (2012) Analysis of nutritional constituents in twenty citrus cultivars from the Mediterranean area at different stages of ripening. Food Nut Sci 03:639–650
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
  • Brennan T, Frenkel C (1977) Involvement of hydrogen peroxide in the regulation of senescence in pear. Plant Physiol 59:411–416
  • Cocetta G, Karppinen K, Suokas M et al (2012) Ascorbic acid metabolism during bilberry (Vaccinium myrtillus L.) fruit development. J Plant Physiol 169:1059–1065
  • Del Rio D, Stewart AJ, Pellegrini N (2005) A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutr Metab Cardiovasc Dis 15:316–328
  • Dhindsa RS, Plumb-Dhindsa P, Thorpe TA (1981) Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation, and decreased levels of superoxide dismutase and catalase. J Exp Bot 32:93–101
  • Echeverria E, Burns JK (1989) Vacuolar acid hydrolysis as a physiological mechanism for sucrose breakdown. Plant Physiol 90:530–533
  • Fanciullino A-L, Dhuique-Mayer C, Luro F et al (2006) Carotenoid diversity in cultivated citrus is highly influenced by genetic factors. J Agric Food Chem 54:4397–4406
  • Fawole OA, Opara UL (2013) Changes in physical properties, chemical and elemental composition and antioxidant capacity of pomegranate (cv. Ruby) fruit at five maturity stages. Sci Hort 150:37–46
  • Foyer CH, Lelandais M, Kunert KJ (1994) Photooxidative stress in plants. Physiol Plant 92:696–717
  • Foyer CH, Lopez-Delgado H, Dat JF, Scott IM (1997) Hydrogen peroxide-and glutathione-associated mechanisms of acclimatory stress tolerance and signalling. Physiol Plant 100:241–254
  • Geigenberger P, Lerchi J, Stitt M, Sonnewald U (1996) Phloemspecific expression of pyrophosphatase inhibits long distance transport of carbohydrates and amino acids in tobacco plants. Plant Cell Environ 19:43–55
  • Gill SS, Tuteja N (2010) Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem 48:909–930
  • Gillespie KM, Ainsworth EA (2007) Measurement of reduced, oxidized and total ascorbate content in plants. Nat Protoc 2:871–874
  • Gulsen O, Roose ML (2001) Chloroplast and nuclear genome analysis of the parentage of lemons. J Am Soc Hortic Sci 126:210–215
  • Haleng J, Pincemail J, Defraigne J-O et al (2007) Le stress oxydant. Rev Med Liege 62:628–638
  • Hamilton GA (1974) Chemical models and mechanism for oxygenases. In: Hayaishi O (ed) Molecular mechanisms of oxygen activation. Academic Press, New York, pp 405–448
  • Hodges DM, DeLong JM, Forney CF, Prange RK (1999) Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 207:604–611
  • Hodges DM, Lester GE, Munro KD, Toivonen PMA (2004) Oxidative stress: importance for postharvest quality. HortScience 39:924–929
  • Huang R, Xia R, Hu L et al (2007) Antioxidant activity and oxygenscavenging system in orange pulp during fruit ripening and maturation. Sci Hort 113:166–172
  • Jiménez A, Hernández JA, Barceló AR et al (1998) Mitochondrial and peroxisomal ascorbate peroxidase of pea leaves. Physiol Plant 104:687–692
  • Katz E, Lagunes PM, Riov J et al (2004) Molecular and physiological evidence suggests the existence of a system II-like pathway of ethylene production in non-climacteric Citrus fruit. Planta 219:243–252
  • López AP, Gochicoa MTN, Franco AR (2010) Activities of antioxidant enzymes during strawberry fruit development and ripening. Biol Plant 54:349–352
  • Lurie S (2003) Antioxidants. In: Hodges DM (ed) Postharvest oxidative stress in horticultural crops. Haworth Press, Inc., New York, pp 131–150
  • Medlicott AP, Reynolds SB, New SW, Thompson AK (1988) Harvest maturity effects on mango fruit ripening. Trop Agric 65:153–157
  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
  • Mondal K, Sharma NS, Malhotra SP et al (2004) Antioxidant systems in ripening tomato fruits. Biol Plant 48:49–53
  • Muller ML, Taiz L (2002) Regulation of the lemon fruit V-ATPase by variable stoichiometry and organic acids. J Membr Biol 185:209–220
  • Nicolosi E, Deng ZN, Gentile A et al (2000) Citrus phylogeny and genetic origin of important species as investigated by molecular markers. Theor Appl Genet 100:1155–1166
  • Nunes-Nesi A, Carrari F, Gibon Y et al (2007) Deficiency of mitochondrial fumarase activity in tomato plants impairs photosynthesis via an effect on stomatal function. Plant J 50:1093–1106
  • Oberley LW, Spitz DR (1984) Assay of superoxide dismutase activity in tumor tissue. Methods Enzymol 105:457–464
  • Peroni LA, Ferreira RR, Figueira A et al (2007) Expression profile of oxidative and antioxidative stress enzymes based on ESTs approach of citrus. Genet Mol Biol 30:872–880
  • Poiroux-Gonord F, Santini J, Fanciullino A-L et al (2013) Metabolism in orange fruits is driven by photooxidative stress in the leaves. Physiol Plant 149:175–187
  • Rahman I, Kode A, Biswas SK (2006) Assay for quantitative determination of glutathione and glutathione disulfide levels using enzymatic recycling method. Nat Prot 1:3159–3165
  • Richardson AC, Marsh KB, Macrae EA (1997) Temperature effects on satsuma mandarin fruit development. J Hortic Sci 72:919–929
  • Sala JM (1998) Involvement of oxidative stress in chilling injury in cold-stored mandarin fruits. Postharvest Biol Techn 13:255–261
  • Sala JM, Lafuente MT (1999) Catalase in the heat-induced chilling tolerance of cold-stored hybrid Fortune mandarin fruits. J Agric Food Chem 47:2410–2414
  • Santini J, Giannettini J, Pailly O et al (2013) Comparison of photosynthesis and antioxidant performance of several Citrus and Fortunella species (Rutaceae) under natural chilling stress. Trees 27:71–83
  • Schantz M-L, Schreiber H, Guillemaut P, Schantz R (1995) Changes in ascorbate peroxidase activities during fruit ripening in Capsicum annuum. FEBS Lett 358:149–152
  • Tompkins D, Toffaletti J (1982) Enzymic determination of citrate in serum and urine, with use of the Worthington ‘‘ultrafree’’ device. Clin Chem 28:192–195
  • Tzur A, Goren R, Zehavi U (1992) Carbohydrate metabolism in developing citrus fruits. Proc Int Soc Citric 1:405–411
  • Uzun A, Yesiloglu T, Tuzcu O, Gulsen O (2009) Genetic diversity and relationships within Citrus and related genera based on sequence related amplified polymorphism markers (SRAPs). Sci Hort 121:306–312
  • Wang SY, Jiao H (2001) Changes in oxygen-scavenging systems and membrane lipid peroxidation during maturation and ripening in blackberry. J Agric Food Chem 49:1612–1619
  • Zhou B, Wang J, Guo Z et al (2006) A simple colorimetric method for determination of hydrogen peroxide in plant tissues. Plant Growth Regul 49:113–118

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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