Nowa wersja platformy, zawierająca wyłącznie zasoby pełnotekstowe, jest już dostępna.
Przejdź na https://bibliotekanauki.pl

PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2018 | 40 | 02 |
Tytuł artykułu

Comparison of jasmine antioxidant system responses to different degrees and durations of shade

Autorzy
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Jasmine [Jasminum sambac (L.) Aiton] growth and development is affected by long-term shade. To determine the effects of short-term shade on jasmine physiology, the contents of soluble proteins, malondialdehyde (MDA) and antioxidative enzymes were comparatively investigated during 24 h (short-term, ST) and 7 days (medium-term, MT) of varying light regimes. The results showed that the protein content exhibited two peaks under ST treatment, and shade postponed the first peak 2 h later than full light. On the whole, protein synthesis was reduced by ST shade and induced by MT shade, whereas MDA content decreased during all shade treatments. Under ST shade, superoxide dismutase (SOD), peroxidase (POD) and ascorbate peroxidase (APX) activities were enhanced, but catalase (CAT) activity was repressed by limited irradiances. However, the antioxidant enzymes responded differently—SOD activity increased after 2 h of shading and then kept on a high level, whereas POD, APX and CAT activities increased mainly during the first hour and deceased subsequently. Under MT shade, these antioxidative enzymes responded differently to varying light irradiances, too. In general, POD and CAT activities were repressed, SOD activity was induced by weak (50% irradiance) shade and reduced by moderate (20% irradiance) and severe (5% irradiance) shade. APX activity was rather more complicated and irregularly responded to different degrees and durations of shade, meaning it might not be the main enzyme to remove ROS in jasmine plants under shading condition. The increase protein content with prolonged shade represents the sound adaptive ability of jasmine plants to restricted irradiances. At the same time, rapid changes in proteins and antioxidants reflect the efficient metabolic apparatus of the plant in response to shade. Therefore, the jasmine cultivar is shade tolerant. Furthermore, shade could help the plants protect themselves from full light, and some degrees of shade were beneficial to their antioxidant system. However, severe shade (5% of irradiance) is only suggested for a few hours to protect the plants at solar noon. If the plants are continuously shaded for 3–7 days, weak (20%) to moderate (50%) level of irradiance should be applied.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
40
Numer
02
Opis fizyczny
Article 41 [6p.], fig.,ref.
Twórcy
autor
  • Institute of Leisure Agriculture, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu, China
autor
  • Institute of Leisure Agriculture, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu, China
autor
  • Institute of Leisure Agriculture, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu, China
autor
  • Institute of Leisure Agriculture, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu, China
autor
  • Institute of Leisure Agriculture, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, Jiangsu, China
Bibliografia
  • Arunachalam V, Reddy DVS (2007) Foliar traits of jasmine plants intercropped in coconut. Agroforest Syst 71:19–23
  • 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
  • Deng YM, Chen SM, Chen FD, Cheng X, Zhang F (2011) The embryo rescue derived intergeneric hybrid between chrysanthemum and Ajania przewalskii shows enhanced cold tolerance. Plant Cell Rep 30:2177–2186
  • Deng YM, Li CC, Shao QS, Ye XQ, She JM (2012a) Differential responses of double petal and multi petal jasmine to shading: I. Photosynthetic characteristics and chloroplast ultrastructure. Plant Physiol Biochem 55:93–102
  • Deng YM, Shao QS, Li CC et al (2012b) Differential responses of double petal and multi petal jasmine to shading: II. Morphology, anatomy and physiology. Sci Hortic 144:19–28
  • Deng YM, Jia XP, Liang LJ, Gu CS, Sun XB (2016) Morphological anatomy, sporogenesis and gametogenesis in flowering process of jasmine (Jasminum sambac Aiton). Sci Hortic 198:257–266
  • Deng YM, Sun XB, Gu CS, Jia XP, Liang LJ, Su JL (2017) Identification of pre-fertilization reproductive barriers and the underlying cytological mechanism in crosses among three petal-types of Jasminum sambac and their relevance to phylogenetic relationships. PLoS One 12(4):e0176026
  • Edris AE, Chizzola R, Franz C (2008) Isolation and characterization of the volatile aroma compounds from the concrete headspace and the absolute of Jasminum sambac (L.) Ait. (Oleaceae) flowers grown in Egypt. Eur Food Res Technol 226:621–626
  • Favaretto VF, Martinez CA, Soriani HH, Furriel RPM (2011) Differential responses of antioxidant enzymes in pioneer and late-successional tropical tree species grown under sun and shade conditions. Environ Exp Bot 70:20–28
  • Foyer CH, Noctor G (2005) Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17:1866–1875
  • Guo WD, Guo YP, Liu JR, Mattson N (2015) Midday depression of photosynthesis is related with carboxylation efficiency decrease and D1 degradation in bayberry (Myrica rubra) plants. Sci Hort 123:188–196
  • Ingham LM, Parker ML, Waldrom KW (1998) Peroxidases: changes in soluble and bound forms during maturation and ripening of apples. Physiol Plant 102:93–100
  • Karuppanapandian T, Moon J, Kim C, Manoharan K, Kim W (2011) Reactive oxygen species in plants: their generation, signal transduction, and scavenging mechanisms. Aust J Crop Sci 5:709–725
  • Maffei ME, Mithofer A, Boland W (2007) Insects feeding on plants: rapid signals and responses preceding the induction of phytochemical release. Phytochem 68:2946–2959
  • Moller IM, Jensen PE, Hansson A (2007) Oxidative modifications to cellular components in plants. Annu Rev Plant Biol 58:459–481
  • Peltzer D, Polle A (2001) Diurnal fluctuations of antioxidative systems in leaves of field-grown beech trees (Fagus sylvatica): response to light and temperature. Physiol Plant 111:158–164
  • Rout NP, Shaw BP (2001) Salt tolerance in aquatic macrophytes: possible involvement of the antioxidative enzymes. Plant Sci 160:415–423
  • Sanmartin M, Pateraki I, Chatzopoulou F, Kanellis AK (2006) Differential expression of the ascorbate oxidase multigene family during fruit development and in response to stress. Planta 225:873–885
  • Sharma P, Dubey RS (2007) Involvement of oxidative stress and role of antioxidative defense system in growing rice seedlings exposed to toxic concentrations of aluminum. Plant Cell Rep 26:2027–2038
  • Yordanova RY, Alexieva VS, Popova LP (2003) Influence of root oxygen deficiency on photosynthesis and antioxidants in barley plants. Russ J Plant Physiol 50:163–167
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-4dabb4f1-6f44-404f-8bc5-73ffc9ba5028
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.