Добавил:
ivanov666
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Элиситоры и их применение в растениеводстве
.pdf
341. The structure and function of a soybean β-glucan elicitor – binding protein /
N. Umemoto [et al.] // Proc. Natl. Acad. Sci. USA. – 1997. – Vol. 94. – P. 1029–1034.
342. Cabrera, J. C. Egg box conformation of oligogalacturonides: The time-dependent stabilization of the elicitor-active conformation increases its biological
activity / J. C. Cabrera [et al.] // Glycobiology. – 2008. – Vol. 18. – P. 473–482.
343. Gómez-Gómez, L. FLS2: An LRR Receptor–like Kinase Involved in the
Perception of the Bacterial Elicitor Flagellin in Arabidopsis / L. Gómez-Gómez,
T. Boller // Mol. Cell. – 2000. – Vol. 5. – P. 1003–1011.
344. Молекулярные основы иммунитета растений / Д. А. Копытина [и др.] //
Биотехнология. Теория и практика. – 2012. – № 3. – С. 31–41.
345. Tena, G. Protein kinase signaling networks in plant innate immunity / G. Tena,
M. Boudsocq, J. Sheen // Curr. Opin. Plant Biol. – 2011. – Vol. 14. – P. 519–529.
346. Nomura, K. Suppression of host defense in compatible plant– Pseudo-
monas syringae interactions / K. Nomura, M. Melotto, S. Y. He // Curr. Opin. Plant
Biol. – 2005. – Vol. 8. – P. 361–368.
347. Gomez-Gomez, L. A single locus determines sensitivity to bacterial
agellin in Arabidopsis thaliana / L. Gomez-Gomez, G. Felix, T. Boller // Plant J. –
1999. – Vol. 18. – P. 277–284.
348. Kim, M. G. Two Pseudomonas syringae type III effectors inhibit RIN4regulated basal defense in Arabidopsis / M. G. Kim [et al.] // Cell. – 2005. – Vol. 121. –
P. 749–759.
349. Ellis, J. G. Flax rust resistance gene specicity is based on direct resistance-avirulence protein interactions / J. G. Ellis, P. N. Dodds, G. J. Lawrence //
Annu. Rev. Phytopathol. – 2007. – Vol. 45. – P. 289–306.
350. Inventory and functional analysis of the large Hrp regulon in Ralstonia
solanacearum: identication of novel effector proteins translocated to plant host
cells through the type III secretion system / S. Cunnac [et al.] // Mol. Microbiol. –
2004. – Vol. 53. – P. 115–128.
351. Closing the circle on the discovery of genes encoding Hrp regulon members and type III secretion system effectors in the genomes of three model Pseudomonas syringae strains / M. Lindeberg [et al.] // Mol. Plant Microbe Interact. –
2006. – Vol. 19. – P. 1151–1158.
352. Zhou, J. M. Plant pathogenic bacterial type III effectors subdue host
responses / J. M. Zhou, J. Chai // Curr. Opin. Microbiol. – 2008. – Vol. 11. – P. 179–185.
353. Takken, F. L. W. Resistance proteins: molecular switches of plant defence /
F. L. W. Takken, M. Albrecht, W. I. L. Tameling // Curr. Opin. Plant Biol. – 2006. –
Vol. 9. – P. 383–390.
354. Lauge, R. Fungal Avirulence Genes: Structure and Possible Functions /
R. Lauge, P. J. De Wit // Fungal Genet. Biol. – 1998. – Vol. 24. – P. 285–297.
355. Collier, S. M. NB-LRRs work a ‘bait and switch’ on pathogens / S. M. Collier, P. Moffett // Trends Plant Sci. – 2009. – Vol. 14. – P. 521–529.
356. Pseudomonas syringae Effector AvrPto Blocks Innate Immunity by Targeting Receptor Kinases / T. Xiang [et al.] // Curr. Biol. – 2008. – Vol. 18. – P. 74–80.
181
357. Keen, N. T. Gene-For-Gene Complementarity in Plant-Pathogen Interac-
tions / N. T. Keen // Annu. Rev. Genet. – 1990. – Vol. 24. – P. 447–463.
358. Plant disease resistance protein signaling: NBS-LRR proteins and their par-
tners / Y. Belkhadir [et al.] // Curr. Opin. Plant Biol. – 2004. – Vol. 7. – P. 391–399.
359. White, F. F. Prospects for understanding avirulence gene function / F. F. White,
B. Yang, L. B. Johnson // Curr. Opin. Plant Biol. – 2000. – Vol. 3. – P. 291–298.
360. Specic Bacterial Suppressors of MA MP Signaling Upstream of MAPKKK
in Arabidopsis Innate Immunit y / P. He [et al.] // Cell. – 2006. – Vol. 125. – P. 563–575.
361. A Pseudomonas syringae Effector Inactivates MAPKs to Suppress PAMPInduced Immunity in Plants / J. Zhang [et al.] // Cell Host Microbe. – 2007. – Vol. 1. –
P. 175–185.
362. Plant Stomata Function in Innate Immunity against Bacterial Invasion /
M. Melotto [et al.] // Cell. – 2006. – Vol. 126. – P. 969–980.
363. Bacterial polysaccharides suppress induced innate immunity by calcium
chelation / S. N. Aslam [et al.] // Curr. Biol. – 2008. – Vol. 18. – P. 1078–1083.
364. Cladosporium fulvum (syn. Passalora fulva), a ighly specialized plant
pathogen as a model for functional studies on plant pathogenic Mycosphaerellaceae /
B. P. H. J. Thomma [et al.] // Mol. Plant Pathol. – 2005. – Vol. 6. – P. 379–393.
365. Saijo, Y. ER quality control of immune receptors and regulators in plants /
Y. Saijo // Cell Microbiol. – 2010. – Vol. 12. – P. 716–724.
366. RIN4 interacts with Pseudomonas syringae type III effector molecules
and is required for RPM1-mediated resistance in Arabidopsis / D. Mackey [et al.] //
Cell. – 2002. – Vol. 108. – P. 743–754.
367. Lukasik, E. Standing strong, resistance proteins instigators of plant defence / E. Lukasik, F. L. Tak ken // Curr. Opin. Plant Biol. – 2009. – Vol. 12. – P. 427– 436.
368. Subterfuge and manipulation: type III effector proteins of phytopathogenic
bacteria / S. R. Grant [et al.] // Annu. Rev. Microbiol. – 2006. – Vol. 60. – P. 425– 449.
369. Zhu, Y. Structural Insights into the Enzymatic Mechanism of the
Pathogenic MAPK Phosphothreonine Lyase / Y. Zhu [et al.] // Mol. Cell. – 2007. –
Vol. 28. – P. 899–913.
370. He, P. Activation of a COI1-dependent pathway in Arabidopsis by Pseudomonas syringae type III effectors and coronatine / P. He [et al.] // Plant J. – 2004. –
Vol. 37. – P. 589–602.
371. Zhang, Y. A Putative Nucleoporin 96 Is Required for Both Basal Defense
and Constitutive Resistance Responses Mediated by suppressor of npr1–1, constitutive 1 / Y. Zhang, X. Li // Plant Cell. – 2005. – Vol. 17. – P. 1306–1316.
372. Tameling, W. I. Physical Association of the NB-LRR Resistance Protein
Rx with a Ran GTPase-Activating Protein Is Required for Extreme Resistance
to Potato virus X / W. I. Tameling, D. C. Baulcombe // Plant Cell. – 2007. – Vol. 19. –
P. 1682 –16 94.
373. Carr, J. P. Signaling in induced resistance / J. P. Carr, M. G. Lewsey,
P. Palukaitis // Adv. Virus Res. – 2010. – Vol. 76. – P. 57–121.
374. Тарчев ский, И. А. Элиситор-индуцируемые сигнальные системы и их
взаимодействие / И. А. Тарчевский // Физиол. раст. – 2000. – Т. 47, № 2. – С. 321–332.
182
375. Van Poecke, R. M. P. Indirect Defence of Plants against Herbivores: Using
Arabidopsis thaliana as a Model Plant / R. M. P. Van Poecke M. Dicke // Plant Biol. –
2004. – Vol. 6. – P. 387–401.
376. Bari, R. Role of plant hormones in plant defence responses / R. Bari,
J. D. Jones // Plant Mol. Biol. – 2009. – Vol. 69. – P. 473–488.
377. Mauch-Mani, B. The role of abscisic acid in plant-pathogen interactions /
B. Mauch-Mani, F. Mauch // Curr. Opin. Plant Biol. – 2005. – Vol. 8. – P. 409–414.
378. Biosynthesis and metabolism of salicylic acid / J. Leon [et al.] // Proc. Natl.
Acad. Sci. USA. – 1995. – Vol. 92, № 4. – P. 4076–4079.
379. Turner, J. G. The Jasmonate Signal Pathway / J. G. Turner, C. Ellis,
A. Devoto // Plant Cell. – 2002. – Vol. 14 (Suppl.). – S. 153–164.
380. Wasternack, C. Jasmonates: An Update on Biosynthesis, Signal Transduc-
tion and Action in Plant Stress Response, Growth and Development / C. Wasternack //
Ann. Bot. – 2007. – Vol. 100. – P. 681–697.
381. Creelman, R. A. Biosynthesis and action of jasmonate in pla nts / R. A. Creel man ,
J. E. Mullet // Annu. Rev. Plant Physiol. Plant Mol. Biol. – 1997. – Vol. 48. – P. 355–387.
382. Васюкова, Н. И. Жасмонат-зависимая защитная сигна лизация в тка-
нях растений / Н. И. Васюкова, О. Л. Озерецковская // Физиол. pастений. –
2009. – Т.56, № 5. – С. 643–653.
383. Narvaez-Vasquez, J. Positional Specicity of a Phospholipase A Activity
Induced by Wounding, Systemin, and Oligosaccharide Elicitors in Tomato Leaves /
J. Narvaez-Vasquez, J. Florin-Christensen, C. A. Ryan // Plant Cell. – 1999. – Vol. 11. –
P. 2249–2260.
384. Browse, J. New Weapons and a Rapid Response against Insect Attack /
J. Browse, G. A. Howe // Plant Physiol. – 2008. – Vol. 146. – P. 832–838.
385. Farmer, E. E. Interplant communication: Airborne methyl jasmonate
induces synthesis of proteinase inhibitors in plant leaves / E. E. Farmer, C. A. Ryan //
Proc. Natl. Acad. Sci. USA. – 1990. – Vol. 87. – P. 7713–7716.
386. Cutting activates a 46-kilodalton protein kinase in plants / S. Usami [et al.] //
Proc. Natl. Acad. Sci. USA. – 1995. – Vol. 92. – P. 8660 –8664.
387. Dinor-oxo-phy todienoic acid: A new hexadecanoid signal in the jasmonate
family / H. Weber [et al.] // Proc. Natl. Acad. Sci. USA. – 1997. – Vol. 94. – P. 10473–10478.
388. Memelink, J. Regulation of gene expression by jasmonate hormones /
J. Memelink // Phytochemistry. – 2009. – Vol. 70. – P. 1560–1570.
389. Van Loon, L. C. Ethylene as a modulator of disease resistance in plants /
L. C. Van Loon, B. P. J. Geraats, H. J. M. Linthorst // Trends Plant Sci. – 2006. –
Vol. 11, № 4. – P. 184–191.
390. Arshad, M. Ethylene, Agricultural Sources and Applications / M. Arshad,
W. T. Jr. Frankenberger. – Kluwer/ Plenum. – 2002.
391. The Role of the Jasmonate Response in Plant Susceptibility to Diverse
Pathogens with a Range of Lifestyles / J. S. Thaler [et al.] // Plant Physiol. – 2004. –
Vol . 135. – P. 530–538.
183
392. Van Poecke, R. M. P Indirect Defence of Plants against Herbivores: Using
Arabidopsis thaliana as a Model Plant / R. M. P. Van Poecke, M. Dicke // Plant Biol. –
2004. – Vol. 6. – P. 387–401.
393. Gutjahr, C. Weights in the Balance: Jasmonic Acid and Salicylic Acid
Signaling in Root-Biotroph Interactions / C. Gutjahr, U. Paszkowski // Mol. Plant
Microbe Interact. – 2009. – Vol. 22. – P. 763–772.
394. Smith, J. L. Jasmonate – and salicylate-mediated plant defense responses
to insect herbivores, pathogens and parasitic plants / J. L. Smith, C. M. De Moraes,
M. C. Mescher // Pest. Manag. Sci. – 2009. – Vol. 65. – P. 497–503.
395. Br uce, T. J. Plant defence signalling induced by biotic attacks / T. J. Bruce,
J. A. Pickett // Curr Opin Plant Biol. – 2007. – Vol. 10. – P. 387–392.
396. Gange, A. C. Arbuscular Mycorrhizal. Fungi Inuence Visitation Rates
of Pollinating Insects / A. C. Gange, A. K. Smith // Ecol. Entomol. – 2005. – Vol. 30. –
P. 600–606.
397. Kessler, A. Herbivore-induced plant vaccination. Part I. The orchestration
of plant defenses in nature and their tness consequences in the wild tobacco Nico-
tiana attenuata / A. Kessler, I. T. Baldwin // Plant J. – 2004. – Vol. 38. – P. 639–649.
398. Salicylate-mediated interactions between pathogens and herbivores / J. S. Thaler [et al.] // Ecology. – 2010. – Vol. 91. – P. 1075–1082.
399. Schoonhoven, L. M. Insect-Plant Biology. Ed 2. / L. M. Schoonhoven,
J. J. A. Van Loon, M. Dicke. – Oxford: Oxford University Press. – 2005.
400. Bostock, R. M. Signal Crosstalk and Induced Resistance: Straddling the
Line Between Cost and Benet / R. M. Bostock // Annu. Rev. Phytopathol. – 2005. –
Vol. 43. – P. 545–580.
401. Direct and interactive effects of enemies and mutualists on plant performance:
A meta-analysis / W. F. Morris [et al.] // Ecology. – 2007. – Vol. 88. – P. 1021–1029.
402. Pitzschke, A. MAPK cascade signalling networks in plant defence / A. Pitzschke, A. Schikora, H. Hirt // Curr. Opin. Plant Biol. – 2009. – Vol. 12. – P. 421– 426.
403. Colcombet, J. Arabidopsis MAPKs: a complex signalling network involved in multiple biological processes / J. Colcombet, H. Hirt // Biochem. J. – 2008. –
Vol. 413. – P. 217–226.
404. Topology of the network integrating salicylate and jasmonate signal
transduction derived from global expression phenotyping / J. Glazebrook [et al.] //
Plant J. – 2003. – Vol. 34. – P. 217–228.
405. Herbivore-Induced Resistance against Microbial Pathogens in Arabidopsis /
M. De Vos [et al.] // Plant Physiol. – 2006. – Vol. 142. – P. 352–363.
406. Quantication, correlations and manipulations of wound-induced changes
in jasmonic acid and nicotine in Nicotiana sylvestris / I. T. Baldwin [et al.] // Planta. –
1997. – Vol. 201. – P. 397– 404.
407. The Outcomes of Concentration-Specic Interactions between Salicylate
and Jasmonate Signaling Include Synergy, Antagonism, and Oxidative Stress Leading
to Cell Death / L. A. J. Mur [et al.] // Plant Physiol. – 2006. – Vol. 140. – P. 249–262.
408. Pieterse, C. M. J. Networking by small-molecule hormones in plant immunity / C. M. J. Pieterse [et al.] // Nat. Chem. Biol. – 2009. – Vol. 5. – P. 308–316.
184
409. Ethylene Modulates the Role of nonexpressor of pathogenesis-related
GENES1 in Cross Talk between Salicylate and Jasmonate Signaling / A. LeonReyes [et al.] // Plant Physiol. – 2009. – Vol. 149. – P. 1797–1809.
410. Polygalacturonase-inhibiting protein accumulates in Phaseolus vulgaris L.
in response to wounding, elicitors, and fungal infection / C. W. Bergmann [et al.] //
Plant J. – 1994. – Vol. 5. – P. 625– 634.
411. Greenberg, J. T. Programmed cell death in plant-pathogen interactions /
J. T. Greenberg // Annu. Rev. Plant Physiol. Plant Mol. Biol. – 1997. – Vol. 48. –
P. 525–545.
412. Отложение каллозы при обработке клеток томатов (Lycopersicon
esculentum L.) биотическими элиситорами / В. И. Емельянов [и др.] // Цитология и генетика. – 2008. – № 2. – C. 21–28.
413. Gage, D. J. Infection and Invasion of Roots by Symbiotic, Nitrogen-Fixing
Rhizobia during Nodulation of Temperate Legumes / D. J. Gage // Microbiol. Mol.
Biol. Rev. – 2004. – Vol. 68. – P. 280 –300.
414. Jabs, T. Mechanisms of Resistance to Plant Diseases / T. Jabs, A. J. Slusarenko // The Hypersensitive Response; (ed.) A. J. Slusarenko, R. S. S. Frazer, L. S. van
Loon Dordrecht. – Kluwer, 2000. – P. 279–324.
415. Полесская, О. Г. Растительная клетка и активные формы кислорода /
О. Г. Полесская. – М.: КДУ, 2007. – 140 с.
416. Колупаев, Ю. Е. Активные формы кислорода в растениях при действии стрессоров: образование и возможные функции / Ю. Е. Колупаев //
Вестн. Харьковского национального аграрного ун-та. Сер. Биология. – 2007. –
Вып. 3. – С. 6–26.
417. Halliwell B. Free Radicals in Biology and Medicine (4th edn) / B. Halliwell,
J. M. C. Gutteridge – Clarendon, 2007. – 312 р.
418. Boller, T. Perception and Transduction of Elicitor Signals in Host – Pathogen Interactions / T. Boller, N. T. Keen // Mechanisms of Resistance to Plant Diseases / (еd.) A. J. Slusarenko, R. S. S. Frazer, L. S. Van Loon. – Dordrecht: Kluwer,
2000. – P. 189–230.
419. Максимов, И. В. Проантиоксидантная система и устойчивость растений к патогенам / И. В. Максимов, Е. А. Черепанова // Усп. cовр. биол. – 2006. –
Т. 126. – С. 250–261.
420. Mittler, R. Oxidative stress, antioxidants and stress tolerance / R. Mittler //
Trends Plant Sci. – 2002. – Vol. 7. – P. 405–410.
421. Growth suppression, altered stomatal responses, and augmented induction
of heat shock proteins in cytosolic ascorbate peroxidase (Apx1)-decient
Arabidopsis plants / L. Pnueli [et al.] // Plant J. – 2003. – Vol. 34, № 2. – P. 187–203.
422. Cho, U. H. Oxidative Stress in Arabidopsis thaliana Exposed to Cadmium
Is due to Hydrogen Peroxide Accumulation / U. H. Cho, N. H. Seo // Plant Science. –
2005. – Vol. 168. – P. 113–120.
423. Moller, I. M. ROS signalling – specicity is required / I. M. Moller, J. Lee //
Trends Plant Sci. – 2010. – Vol. 15. – P. 370–374.
185
424. Oxidative modications to cellular components in plants / I. M. Moller
[et al.] // Annu. Rev. Plant Biol. – 2007. – Vol. 58. – P. 459–481.
425. Transcriptomic footprints disclose specicity of reactive oxygen species
signaling in Arabidopsis / I. Gadjev [et al.] // Plant Physiol. – 2006. – Vol. 141. –
P. 436– 445.
426. ROS signaling: the new wave? / R. Mittler [et al.] // Trends Plant Sci. –
2011. – Vol. 16. – P. 300 –309.
427. Малиновский, В. И. Механизмы устойчивости растений к вирусам /
В. И. Малиновский. – Владивосток: Дальнаука, 2010. – 324 с.
428. Van Loon, L. C. The families of pathogenesis-related proteins, their activities, and comparative analysis of PR-1 type proteins / L. C. Van Loon, E. A. Van Strien //
Physiol. Mol. Plant Pathol. – 1999. – Vol. 55. – P. 85–97.
429. Механизмы индукции резистентности растений к фитопатогенным
гуминовым веществам / С. Н. Удинцев [и др.] // Вестн. Томского гос. ун-та.
Биология. – 2011. – № 4. – С. 100–107.
430. Van der Hoorn, R. A. L. Plant proteases: from phenotypes to molecular
mechanisms / R. A. L. Van der Hoorn // Annu. Rev. Plant Biol. – 2008. – Vol. 59. –
P. 191–223.
431. Тарчевский, И. А. Сигнальные системы клеток растений / И. А. Тарчевский. – М.: Наука, 2002. – 294 с.
432. Трифонова, Е. А. Роль нуклеаз в физиологических процессах высших растений / Е. А. Трифонова, А. В. Кочетов, В. К. Шумный // Усп. соврем.
Биол. – 2000. – Т. 120. – С. 395–405.
433. Bowles, D. J. Defense-Related Proteins in Higher Plants / D. J. Bowles //
Annu. Rev. Biochem. – 1990. – Vol. 59. – P. 873–900.
434. Novel Acidic Sesquiterpenoids Constitute a Dominant Class of PathogenInduced Phytoalexins in Maize / A. Huffaker [et al.] // Plant Physiol. – 2011. –
Vol. 156. – P. 2082–2097.
435. Muller, K. O. Experimentelle Untersuchungen über die Phytophthora –
Resistenz der Kartoffel / K. O. Muller, H. Burger // Panzenreich. Arbeiten der Biologischen Reichsanstalt fur Land – und Forstwirtschaft. – 1940. – Vol. 23. – S. 189–231.
436. An ABC transporter and a cytochrome P450 of Nectria haematococca
MPVI are virulence factors on pea and are the major tolerance mechanisms to the
phytoalexin pisatin / J. J. Coleman [et al.] // Mol. Plant Microbe Interact. – 2011. –
Vol. 24. – P. 368–376.
437. Ahuja, I. Phytoalexins in defense against pathogens / I. Ahuja, R. Kissen,
M. Atle // Plant Science. – 2012. – Vol. 17, № 2. – P. 73–90.
438. Resistance of cotton towards Xanthomonas campestris pv. malvacearum /
E. Delannoy [et al.] // Annu. Rev. Phytopathol. – 2005. – Vol. 43. – P. 63–82.
439. Kauss, H. Callose synthesis / H. Kauss // Membranes: Specialized Functions in Plants. – Guildford: Bios Sci. Publ, 1996. – P. 77–92.
440. Bittel, P. Microbe-associated molecular patterns (MAMPs) probe plant immunity / P. Bittel, S. Robatzek // Curr. Opin. Plant Biol. – 2007. – Vol. 10. – P. 335–341.
186
441. Watt, S. A. Identication of the bacterial superoxide dismutase (SodM) as
plant-inducible elicitor of an oxidative burst reaction in tobacco cell suspension
cultures / S. A. Watt [et al.] // J. Biotechnol. – 2006. – Vol. 126. – P. 78–86.
442. Schuhegger, R. Induction of systemic resistance in tomato by N-acyl-L-
homoserine lactone-producing rhizosphere bacteria / R. Schuhegger [et al.] // Plant
Cell Environ. – 2006. – Vol. 29. – P. 909–918.
443. Recent progress in discovery and functional analysis of effector proteins
of fungal and oomycete plant pathogens / J. G. Ellis [et al.] // Curr. Opin. Plant Biol. –
2009. – Vol. 12. – P. 399–405.
444. Molecular Evolution of Lysin Motif-Type Receptor-Like Kinases in Plants /
X.-C. Zhang [et al.] // Plant Physiol. – 2007. – Vol. 144. – P. 623–636.
445. Molecular Basis of Ergosterol-Induced Protection of Grape Against Botrytis cinerea: Induction of Type I LTP Promoter Activity, WRKY, and Stilbene
Synthase Gene Expression / L. Laquitine [et al.] // Mol. Plant-Microbe Interact. –
2006. – Vol. 19. – P. 1103–1112.
446. Host-Pathogen Interactions / M. Kopp [et al.] // Plant Physiol. – 1989. –
Vol. 90. – P. 208 – 216.
447. Ферментативная трансформация биологически активного 1,3; 1,6-βD-глюкана. Структура и активность полученных фрагментов / Л. А. Елякова
[и др.] // Биохимия. – 2007. – Т. 72. – С. 36–44.
448. Stubler, D. Antiviral activity of the glucan lichenan (poly-β-(1–3,1–4)-Danhydroglucose). I. Biological activity in tobacco plants / D. Stubler, H. J. Buchenauer //
J. Phytopathol. – 1996. – Vol. 144. – P. 37– 43.
449. Effect of κ/λ – carrageenan from red a lga Tichocarpus crinitus (Tichocarpaceae) on infection of detached tobacco leaves with tobacco mosaic virus /
A. V. Reunov [et al.] // J. Plant Disc. Protect. – 2004. – Vol. 111. – P. 165–172.
450. Лапшина, Л. А. Ингибирующее действие фукоидана из бурой водоросли Fucus evanescens на развитие инфекции, вызванной вирусом табачной
мозаики в листьях двух сортов табака / Л. А. Лапшина // Физиология растений. – 2006. – Т. 53. – С. 274–279.
451. Kang, B.-C. Genetics of Plant Virus Resistance / B.-C. Kang, Y. Inhwa,
M. Molly // Annu. Rev. Phytopathol. – 2005. – Vol. 43. – P. 581–621.
452. Kachroo, P. Plant signal transduction and defense against viral pathogens /
P. Kachroo, A. C. Chandra-Shekara, D. F. Klessig // Adv. Virus Res. – 2006. – Vol. 66. –
P. 161–191.
453. Maule, A. The dialogue between viruses and hosts in compatible interactions / A. Maule, V. Leh, C. Lederer // Curr. Opin. Plant Biol. – 2002. – Vol. 5. –
P. 279–284.
454. Lnduction of a Highly Specic Antiviral State in Transgenic Plants:
lmplications for Regulation of Gene Expression and Vir us Resistance / J. A. Lindbo
[et al.] // Plant Cell. – 1993. – Vol. 5. – P. 1749–1759.
455. Vaucheret, H. Post-transcriptional gene silencing in plants / H. Vaucheret,
C. Beclin, M. Fagard // J. Cell Sci. – 2001. – Vol. 114. – P. 3083–3091.
187
456. Jones-Rhoades, M. W. MicroRNAS and their regulatory roles in plants /
M. W. Jones-Rhoades, D. P. Bartel, B. Bartel // Annu. Rev. Plant Biol. – 2006. –
Vol. 57. – P. 19–53.
457. Waterhouse, P. M. Gene silencing as an adaptive defence against viruses /
P. M. Waterhouse, M. B Wang, T. Lough // Nature. – 2001. – Vol. 411. – P. 834–842.
458. Williamson, V. M. Plant-nematode interactions / V. M. Williamson,
C. A. Gleason // Curr. Opin. Plant Biol. – 2003. – Vol. 6. – P. 327–333.
459. Bellaore, S. Nematode effectors and plant responses to infection / S. Bellaore, S. P. Briggs // Curr. Opin. Plant Biol. – 2010. – Vol. 13. – P. 442–448.
460. Зиновьева, С. В. Биохимические аспекты взаимодействия растений
с паразитическими нематодами (обзор) / С. В. Зиновьева, Н. И. Васюкова,
О. Л. Озерецковская // Прикл. биохим. и микробиол. – 2004. – Т. 40, № 2. –
С. 133–142.
461. Williamson, V. M. Plant nematode resistance genes / V. M. Williamson //
Curr Opin Plant Biol. – 1999. – Vol. 2. – P. 327–331.
462. Williamson, V. M. Nematode resistance in plants: the battle underground /
V. M. Williamson, A. Kumar // Trends Genet. – 2006. – Vol. 22. – P. 396– 403.
463. Effects of Feeding Spodoptera littoralis on Lima Bean Leaves. II.
Continuous Mechanical Wounding Resembling Insect Feeding Is Sufcient to Elicit
Herbivory-Related Volatile Emission / A. Mithoffer [et al.] // Plant Physiol. – 2005. –
Vol. 137. – P. 1160–1168.
464. Li, M. Phospholipase D – and phosphatidic acid-mediated signaling in plants /
M. Li, Y. Hong, X. Wang // BBA. – 2009. – Vol. 179. – P. 927–935.
465. Sun, J.-Q. Systemi n/Jasmonate-mediated system ic defense signaling in to mato / J.-Q. Sun, H.-L. Jiang, C.-Y. Li // Mol. Plant. – 2011. – Vol. 4. – P. 607–615.
466. Ryan, C. A. The systemin signaling pathway : diferential activation of plant
defensive genes / C. A. Ryan // Biochim. Biophys. Acta. – 2000. – № 1477. – P. 112–121.
467. Ryan, C. A. Assay and Biochemical Properties of the Proteinase Inhibitor–
Inducing Factor, a Wound Hormone / C. A. Ryan // Plant Physiology. – 1974. –
Vol. 54. – P. 328–332.
468. Ryan, C. A. The search for the proteinase-inhibitor inducing factor, PIIF /
C. A. Ryan // Plant Mol. Biol. – 1992. – Vol. 19. – P. 123–133.
469. A wound – and systemin-inducible polygalacturonase in tomato leaves /
D. R. Bergey [et al.] // Proc. Natl. Acad. Sci. USA. – 1999. – Vol. 96. – P. 1756–1760.
470. Ueda, J. Isolation and identication of senescence-promoting substances
from wormwood (Artemisia absinthium L.) / J. Ueda, J. Kato // Plant Physiol. –
1980. – Vol. 66. – P. 246–249.
471. Farmer, E. E. Regulation of expression of proteinase inhibitor genes by
methyl jasmonate and jasmonic acid / E. E. Farmer, R. R. Johnson, C. A. Ryan //
Plant Physiol. – 1992. – Vol. 98. – P. 995–1002.
472. Differential Gene Expression in Response to Mechanical Wounding and
Insect Feeding in Arabidopsis / P. Reymond [et al.] // Plant Cell. – 2000. – Vol. 12. –
P. 707–719.
188
473. Green, T. R. Wound-Induced Proteinase Inhibitor in Plant Leaves-Possible
Defense Mechanism against Insects / T. R. Green, C. A. Ryan // Science. – 1972. –
Vol. 175. – P. 776–777.
474. Bowles, D. Signal transduction in the wound response of tomato plants /
D. Bowles // Phil. Trans. R. Soc. – 1998. – Vol. 353. – P. 1495–1510.
475. Ryan, C. A. Systemin: A polypeptide signal for plant defensive genes /
C. A. Ryan, G. Pearce // Annu. Rev. Cell Dev. Biol. – 1998. – Vol. 14. – P. 1–17.
476. Schaller, A. Modulation of Plasma Membrane H+-ATPase Activity Differentially Activates Wound and Pathogen Defense Responses in Tomato Plants /
A. Schaller, C. Oecking // Plant Cell. – 1999. – Vol. 11. – P. 263–272.
477. Farme, E. E. Octadecanoid Precursors of Jasmonic Acid Activate the
Synthesis of Wound-lnducible Proteinase lnhibitors / E. E. Farme, C. A. Ryan //
Plant Cell. – 1992. – Vol. 4. – P. 129–134.
478. Scheer, J. M. Generation of systemin signaling in tobacco by transformation with the tomato systemin receptor kinase gene / J. M. Scheer, G. Pearce,
C. A. Ryan // Proc. Natl. Acad. Sci. USA. – 2003. – Vol. 100. – P. 10114–10117.
479. Li, C. The Tomato Suppressor of prosystemin-mediated responses2 Gene
Encodes a Fatty Acid Desaturase Required for the Biosynthesis of Jasmonic Acid
and the Production of a Systemic Wound Signal for Defense Gene Expression /
C. Li [et al.] // Plant Cell. – 2003. – Vol. 15. – P. 1646 –1661.
480. Koo, A. J. K. The wound hormone jasmonate / A. J. K. Koo, G. А. Howe //
Phytochemistry. – 2009. – Vol. 70. – P. 1571–1580.
481. Heil, M. Indirect defence via tritrophic interactions / M. Heil // New
Phytol. – 2008. – Vol. 178. – P. 41–61.
482. Young, T. P. Increased thorn length in Acacia depranolobium – an induced
response to browsing / T. P. Young // Oecologia. – 1987. – Vol. 71. – P. 436– 438.
483. Hilker, M. Early herbivore alert: Insect eggs induce plant defense /
M. Hilker, T. Meiners // J. Chem. Ecol. – 2006. – Vol. 32. – P. 1379–1397.
484. Oviposition by Pierid Butteries Triggers Defense Responses in Arabi-
dopsis / D. Little [et al.] // Plant Physiol. – 2007. – Vol. 143. – P. 784–800.
485. Vet, L. E. M. Ecology of infochemical use by natural enemies in a tritrophic context / L. E. M. Vet, M. Dicke // Ann. Rev. Entomol. – 1992. – Vol. 37. –
P. 141–172.
486. Fatouros, N. E. Foraging behavior of egg parasitoids exploiting chemical
information / N. E. Fatouros [et al.] // Behav. Ecol. – 2008. – Vol. 19. – P. 677– 689.
487. Agrawal, A. A. Induced responses to herbivory in wild radish: Effects on
several herbivores and plant t-ness / A. A. Agrawal // Ecology. – 1999. – Vol. 80. –
P. 1713 –172 3.
488. Kester, K. M. Behavioral and ecological constraints imposed by plants on
insect parasitoids: Implications for biological control / K. M. Kester, P. Barbosa //
Biol. Control. – 1991. – Vol. 1. – P. 94–106.
489. Goellner, K. Priming: it’s all the world to induced disease resistance /
K. Goellner, U. Conrath // Eur. J. Plant Pathol. – 2008. – Vol. 121, № 3. – P. 233–242.
189
490. Lucas, J. A. Advances in plant disease and pest management / J. A. Lucas //
J. Agric. Sci. – 2011. – Vol. 149. – P. 91–114.
491. Effects of Feeding Spodoptera littoralis on Lima Bean Leaves. I. Membrane Potentials, Intracellular Calcium Variations, Oral Secretions, and Regurgitate
Components / M. E. Maffei [et al.] // Plant Physiol. – 2004. – Vol. 134. – P. 1752–1762.
492. Effects of Feeding Spodoptera littoralis on Lima Bean Leaves. III. Membrane Depolarization and Involvement of Hydrogen Peroxide / M. E. Maffei [et al.] //
Plant Physiol. – 2006. – Vol. 140. – P. 1022–1035.
493. Herbivory rapidly activates MAPK signaling in attacked and unattacked
leaf regions but not between leaves of Nicotiana attenuata / J. Q. Wu [et al.] // Plant
Cell. – 2007. – Vol. 19. – P. 1096–1122.
494. Merging molecular and ecological approaches in plant-insect interactions /
I. T. Baldwin [et al.] // Curr. Opin. Plant Biol. – 2001. – Vol. 4. – P. 351–358.
495. de Bruxelles, G. L. Signals regulating multiple responses to wounding
and herbivores / G. L. De Bruxelles, M. R. Roberts // Crit. Rev. Plant Sci. – 2001. –
Vol. 20. – P. 487–521.
496. Furstenberg-Hagg J. Plant Defense against Insect Herbivores / J. Furstenberg-Hagg, M. Zagrobelny, S. Bak // Int. J. Mol. Sci. – 2013. – Vol. 14. – P. 10242–10297.
497. Schmelz, E. A. The inuence of intact-plant and excised-leaf bioassay
designs on volicitin – and jasmonic acid-induced sesquiterpene volatile release
in Zea mays / E. A. Schmelz, H. T. Alborn, J. H. Tumlinson // Planta. – 2001. –
Vol. 214. – P. 171–179.
498. Molecular Interactions between the Specialist Herbivore Manduca sexta
(Lepidoptera, Sphingidae) and Its Natural Host Nicotiana attenuata. III. Fatty AcidAmino Acid Conjugates in Herbivore Oral Secretions Are Necessary and Sufcient
for Herbivore-Specic Plant Responses / R. Halitschke [et al.] // Plant Physiol. –
2001. – Vol. 125. – P. 711–717.
499. Major, I. T. Molecular analysis of poplar defense against herbivory:
Comparison of wound – and insect elicitor-induced gene expression / I. T. Major,
C. P. Constabel // New Phytol. – 2006. – Vol. 172. – P. 617–635.
500. Identication of volatiles that are used in discrimination between plants
infested with prey or nonprey herbivores by a predatory mite / J. G. De Boer [et al.] //
J. Chem. Ecol. – 2004. – Vol. 30. – P. 2215–2230.
501. Felton, G. W. Plant-insect dialogs: Complex interactions at the plant-insect
interface / G. W. Felton, J. H. Tumlinson // Curr. Opin. Plant Biol. – 2008. – Vol. 11. –
P. 457–463.
502. Evidence that the caterpillar salivary enzyme glucose oxidase provides
herbivore offense in solanaceous plants / R. O. Musser [et al.] // Arch. Insect. Biochem. Physiol. – 2005. – Vol. 58. – P. 128–137.
503. Herbivore-induced volatiles: The emission of acyclic homoterpenes from
leaves of Phaseolus lunatus and Zea mays can be triggered by a β-glucosidase and
jasmonic acid / J. Hopke [et al.] // FEBS Lett. – 1994. – Vol. 352. – P. 146–150.
504. Fatty acid-amino acid conjugates diversication in lepidopteran
caterpillars / N. Yoshinaga [et al.] // J. Chem. Ecol. – 2010. – Vol. 36. – P. 319–325.
190
Соседние файлы в предмете [НЕСОРТИРОВАННОЕ]