PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2006 | 28 | 5 |

Tytuł artykułu

Effect of abscisic acid and ontogenic phases of the host alga on the infection process in the pathosystem Scenedesmus acutus - Phlyctidium scenedesmi

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The parasite contamination make difficult laboratory cultivation of green algae and decrease significantly the production of microalgal biomass during industrial cultivation. In the present study the influence of the endogenous abscisic acid content (determinate by gas chromatography) on the host-parasite relationship in different ontogenetic phases of the host Scenedesmus as well as resistance induction after treatment of synchronous algal culture with ABA were studied. Synchronization of algae was carried out by alteration of light and dark periods. The age groups under study were: autospores (at the beginning of the light period), growing cells, mature cells (belonging to in the end of the light period) and mature cells, starting to release autospore at the beginning of dark phases. The higher levels of endogenous ABA during the algal autospore formation as well as exogenous ABA supply of (10-5 M) inhibited the infection process in the pathosystem green microalga Scenedesmus acutus and unicellular fungal parasite Phlyctidium scenedesmi. The treatment with fluridone 10-7 M (an inhibitor ofABA biosynthesis) increased the host susceptibiltty during all ontogenetic phases. The susceptibiltty of S. acutus to the chytridial infection depended on the endogenous ABA level during different ontogenetic stages of the alga.

Wydawca

-

Rocznik

Tom

28

Numer

5

Opis fizyczny

p.395-400,fig.,ref.

Twórcy

autor
  • Bulgarian Academy of Sciences, Sofia 1113, Bulgaria

Bibliografia

  • Apostol I., Heinstein P.F. and Low P.S. 1989. Rapid stimulation of an oxidative burst during elicitation of cultured plant cells. Role in defense and signal transduction. Plant Physiol. 90: 109-116.
  • Audenaert K., Meyer G.B.De and Hofte M.M. 2002. Abscisic acid determines basal susceptibility of tomato to Botrytis cinerea and suppresses salicylic acid-det pendent signaling mechanisms. Plant Physiol. 128: 491-501.
  • Baker C.J. and Orlandi E.W. 1995. Active oxygen in plant pathogenesis. Ann. Rev. Phytopathol. 33: 299-321.
  • Benderliev K.M., Pouneva I.D. and Ivanova N.I. 1993. Fungicide effect of triton-N on Phlyctidium. Biotechnol. Techniques 7: 335-338.
  • Bolwell G.P., Bindschedler L.V., Blee K.A., Butt V.S., Davies D.R., Gardner S.L., Gerrish C. and Minibayeva F. 2002. The apoplastic oxidative burst in response to biotic stress in plants: a three-component system. J. Exp. Bot. 1367-1376.
  • Dunn R.M., Hedden P. and Bailey J.A. 1990. A physiologically-induced resistance of Phaseolus vulgaris to a compatible race of Colletotrichum lindemuthianum is associated with increases in ABA content. Physiol. Mol. Plant Pathol. 36: 339-349.
  • Fraser R.S.S. 1993. ABA and plant responses to pathogens. In: Jones, H.J., Davies, W.J. (ed.): ABA: Physioloigy and Biochemistry. Pp. 189-199. Oxford: Bios Scientific Publishers, UK
  • Genoud T., Santa Cruz M.B.T. end Metraux, J.-P. Numeric simulation of plant signaling networks. Plant Physiol. 126: 1430-1437.
  • Hirsch R., Hartung W. and Gimmler H. 1989. Abscisic acid content of algae under stress. Bot. Acta 102: 326-334.
  • Ilkov G. 1975. Population dynamic relationships during Phlyctidium scenedesmi development in Scenedesmus acutus cultures. Appl. Microbiol. 6: 104-110 [in Bulgarian].
  • Jiang M. and Zhang J. 2001. Effect of abscisic acid on active oxygen species, antioxidative defense system and oxidative damage in leaves of maize seedlings. Plant and Cell Physiol. 42: 1265-1273.
  • Kauss H., Jeblick W., Ziegler J. and Krabler W. 1994. Pretreatment of parsley (Petroselinum crispum L.) suspention cultures with methyl jasmonate enhances elicitation of activated oxygen species. Plant Physiol. 105: 89-94.
  • Kettner J. and Dorffling K. 1995.Biosynthesis and metabotism of abscisic acid in tomato leaves infected with Botrytis cinerea. Planta 196: 627-634.
  • Kobayashi M., Hirai N., Kurimura Y., Ohigashi H. and Tsuji Y.1997. Abscisic acid-dependent algal morphogenesis in the unicellular green alga Haematococcus pluvialis. Plant Gr. Regul. 22: 79-85.
  • Low P.S. and Heinstein P.F. 1986. Elicitor stimulation of the defense response in cultured plant cells monitored by fluorescent dyes. Arch. Biochem. Biophys. 249: 472479.
  • Mallick N. and Mohn F.H. 2000. Reactive oxygen species: responses of algal cells. J. Plant Physiol. 157: 183-193.
  • McDonald K.L. and Cahill D.M. 1999. Influence of abscisic acid and the abscisic acid biosynthesis inhibitor, norflurason, on interaction between Phytophthora sojae and soybean (Glycine max). Eur. J. Plant Pathol. 105: 651-658.
  • McDonald K.L., Sutherl and M.W. and Guest, D.I. Temporary hypoxia suppresses the oxidative burst and subsequent hypersensitive cell death in cells of tobacco and soybean challenged with zoospores of incompatible isolates of Phytophthora species. Physiol. and Mol. Plant Pathol. 61: 133-140.
  • Murata Y., Pei Z.-M., Mori I.C. and Schroder J. 2001. Abscisic acid activation of plasma membrane Ca2+ channels in guard cells requires cytosolic NAD(P)H and is differentially disrupted upstream and downstream of reactive oxygen species production in abl1-1 and abl2-1 protein phosphatase 2C mutants. The Plant Cell 13: 2513-2523.
  • Popova L.P. and Riddle K.A. 1996. Development and accumulation of ABA in fluridone-treated and drought stressed Vicia faba plants under different light conditions. Physiol. Plant. 98: 791-797.
  • Pospisilova J. and Batkova P. 2004. Effect of pre-treatments with abscisic acid and/or benzyladenine on gas exchanges of French bean, sugar beet, and maize leaves during water stress and after rehydratation. Biol. Plant. 48: 395-399.
  • Ryerson E., Li A., Young J.P. and Heath M.C. 1993. Changes in abscisic acid levels during the initial stages of host and non-host reactions to the rust fungus. Physiol. Mol. Plant Pathol. 43: 265-273.
  • Shinogi T., Suzuki T., Kurihara T., Narusaka Y. and Park P. 2003. Microscopic detection of reactive oxygen species generation in the compatible and incompatible interaction of Alternaria alternata Japanese pear patho- type and host plants. J. Gen. Plant Pathol. 69: 7-16.
  • Singh P.P., Basra A.S. and Pannu P.P.S. 1997. Abscisic acid is a potential inhibitor on growth and sporidial formation in Nevossisia indica cultures: Dual mode of action via loss of polyamines and cellular turgidity. Phytoparasitica 25: 111-116.
  • Steadman J.R. and Sequeira L. 1970. Abscisic acid in tobacco plants: tentative identification and its relation to stunting induced by Pseudomonas solanacearum. Plant Physiol. 45: 691-697.
  • Tietz A., Ruttkowski U., Kohler R. and Kasprik W. 1989. Further investigation on the occurrence and the effects of abscisic acid in algae. Biochem. Physiol. Pflanzen. 184: 259-266.
  • Whenham R.J., Fraser R.S.S., Brown L.P. and Payne J.A. 1986. Tobacco mosaic virus-induced increase in abscisic acid concentration in tobacco leaves: intracellular location in light and darkgreen areas, and relationship to symptom development. Planta 168: 592-598.
  • Yoshida K., Igarashi E., Wakatsuki E., Miyamoto K. and Hirata K. 2004. Mitigation of osmotic and salt stress by abscisic acid through reduction of stress-derived oxidative damage in Chlamydomonas reinhardtii. Plant Science 167: 1335-1341.
  • Yoshioka T., Endo T. and Satoh S. 1998. Restoration of seed germination at supraoptimal temperatures by fluridone, an inhibitor of abscisic acid biosynthesis. Plant Cell Physiol. 39: 307-312.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-bb6b9792-281c-4f4c-857a-99440c54428d
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.