Literature DB >> 12232004

Developmental Variability of Photooxidative Stress Tolerance in Paraquat-Resistant Conyza.

Z. Amsellem1, MAK. Jansen, ARJ. Driesenaar, J. Gressel.   

Abstract

Paraquat-resistant hairy fleabane (Conyza bonariensis L. Cronq.) has been extensively studied, with some contention. A single, dominant gene pleiotropically controls levels of oxidant-detoxifying enzymes and tolerance to many photooxidants, to photoinhibition, and possibly to other stresses. The weed forms a rosette on humid short days and flowers in dry long days and, thus, needs plasticity to photooxidant stresses. In a series of four experiments over 20 months, the resistant and susceptible biotypes were cultured in constant 10-h low-light short days at 25[deg]C. Resistance was measured as recovery from paraquat. The concentration required to achieve 50% inhibition of the resistant biotype was about 30 times that of the susceptible one just after germination, increased to >300 times that of the susceptibles at 10 weeks of growth, and then decreased to 20-fold, remaining constant except for a brief increase while bolting. Resistance increased when plants were induced to flower by long days. The levels of plastid superoxide dismutase and of glutathione reductase were generally highest in resistant plants compared to those of the susceptibles at the times of highest paraquat resistance, but they were imperceptibly different from the susceptible type at the times of lower paraquat resistance. Photoinhibition tolerance measured as quantum yield of oxygen evolution at ambient temperatures was highest when the relative amounts of enzymes were highest in the resistant biotype. Resistance to photoinhibition was not detected by chlorophyll a fluorescence. Enzyme levels, photoinhibition tolerance, and paraquat resistance all increased during flowering in both biotypes. Imperceptibly small increases in enzyme levels would be needed for 20-fold resistance, based on the moderate enzyme increases correlated with 300-fold resistance. Thus, it is feasible that either these enzymes play a role in the first line of defense against photooxidants, or another, yet unknown mechanism(s) facilitate(s) the lower level of resistance, or the enzymes and unknown mechanisms act together.

Entities:  

Year:  1993        PMID: 12232004      PMCID: PMC159094          DOI: 10.1104/pp.103.4.1097

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  15 in total

1.  COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS.

Authors:  D I Arnon
Journal:  Plant Physiol       Date:  1949-01       Impact factor: 8.340

2.  Plant morphological and biochemical responses to field water deficits: I. Responses of glutathione reductase activity and paraquat sensitivity.

Authors:  J J Burke; P E Gamble; J L Hatfield; J E Quisenberry
Journal:  Plant Physiol       Date:  1985-10       Impact factor: 8.340

3.  Isozymes of superoxide dismutase from wheat germ.

Authors:  C O Beauchamp; I Fridovich
Journal:  Biochim Biophys Acta       Date:  1973-07-12

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  Kinetic Analysis of Resistance to Paraquat in Conyza: Evidence that Paraquat Transiently Inhibits Leaf Chloroplast Reactions in Resistant Plants.

Authors:  Y Shaaltiel; J Gressel
Journal:  Plant Physiol       Date:  1987-12       Impact factor: 8.340

6.  Biochemical Studies of Paraquat-Tolerant Mutants of the Fern Ceratopteris richardii.

Authors:  E W Carroll; O J Schwarz; L G Hickok
Journal:  Plant Physiol       Date:  1988-07       Impact factor: 8.340

7.  Increased Tolerance to Photoinhibitory Light in Paraquat-Resistant Conyza bonariensis Measured by Photoacoustic Spectroscopy and CO(2)-Fixation.

Authors:  M A Jansen; Y Shaaltiel; D Kazzes; O Canaani; S Malkin; J Gressel
Journal:  Plant Physiol       Date:  1989-11       Impact factor: 8.340

8.  Chilling-enhanced photooxidation : evidence for the role of singlet oxygen and superoxide in the breakdown of pigments and endogenous antioxidants.

Authors:  R R Wise; A W Naylor
Journal:  Plant Physiol       Date:  1987-02       Impact factor: 8.340

9.  On the Mechanism of Resistance to Paraquat in Hordeum glaucum and H. leporinum: Delayed Inhibition of Photosynthetic O(2) Evolution after Paraquat Application.

Authors:  C Preston; J A Holtum; S B Powles
Journal:  Plant Physiol       Date:  1992-10       Impact factor: 8.340

10.  Superoxide as an intracellular radical sink.

Authors:  C C Winterbourn
Journal:  Free Radic Biol Med       Date:  1993-01       Impact factor: 7.376

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  4 in total

1.  Responses of Antioxidants to Paraquat in Pea Leaves (Relationships to Resistance).

Authors:  J. L. Donahue; C. M. Okpodu; C. L. Cramer; E. A. Grabau; R. G. Alscher
Journal:  Plant Physiol       Date:  1997-01       Impact factor: 8.340

2.  Constitutively Elevated Levels of Putrescine and Putrescine-Generating Enzymes Correlated with Oxidant Stress Resistance in Conyza bonariensis and Wheat.

Authors:  B. Ye; H. H. Muller; J. Zhang; J. Gressel
Journal:  Plant Physiol       Date:  1997-12       Impact factor: 8.340

3.  Enhanced sensitivity to oxidative stress in transgenic tobacco plants with decreased glutathione reductase activity leads to a decrease in ascorbate pool and ascorbate redox state.

Authors:  Shunhua Ding; Qingtao Lu; Yan Zhang; Zhipan Yang; Xiaogang Wen; Lixin Zhang; Congming Lu
Journal:  Plant Mol Biol       Date:  2008-11-29       Impact factor: 4.076

4.  Paraquat Resistant1, a Golgi-localized putative transporter protein, is involved in intracellular transport of paraquat.

Authors:  Jianyong Li; Jinye Mu; Jiaoteng Bai; Fuyou Fu; Tingting Zou; Fengying An; Jian Zhang; Hongwei Jing; Qing Wang; Zhen Li; Shuhua Yang; Jianru Zuo
Journal:  Plant Physiol       Date:  2013-03-07       Impact factor: 8.340

  4 in total

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