Catabolism of volatile organic compounds influences plant survival

Trends in Plant Science

Volumn 18, Issue 12, 2013, Pages 695-703

  Oikawa, Patricia Y ^a   Lerdau, Manuel T ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

Author keywords

Air pollution; Catabolism; Phytogenic volatile organic compounds (VOCs); Plant C balance; Tolerance; VOC emission models

Indexed keywords

CARBON; VOLATILE ORGANIC COMPOUND;

AIR POLLUTION; ATMOSPHERE; CATABOLISM; METABOLISM; PHYSIOLOGICAL STRESS; PHYTOGENIC VOLATILE ORGANIC COMPOUNDS (VOCS); PLANT; PLANT C BALANCE; REVIEW; SIGNAL TRANSDUCTION; TOLERANCE; VOC EMISSION MODELS;

AIR POLLUTION; CATABOLISM; PHYTOGENIC VOLATILE ORGANIC COMPOUNDS (VOCS); PLANT C BALANCE; TOLERANCE; VOC EMISSION MODELS;

ATMOSPHERE; CARBON; METABOLIC NETWORKS AND PATHWAYS; PLANTS; SIGNAL TRANSDUCTION; STRESS, PHYSIOLOGICAL; VOLATILE ORGANIC COMPOUNDS;

EID: 84888427795     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2013.08.011     Document Type: Review

References (80)

1. Guenther A., et al. A global-model of natural volatile organic-compound emissions. J. Geophys. Res. 1995, 100:8873-8892.
2. Harrison S.P., et al. Volatile isoprenoid emissions from plastid to planet. New Phytol. 2013, 197:49-57.
3. Peñuelas J., Llusià J. BVOCs: plant defense against climate warming?. Trends Plant Sci. 2003, 8:105-109.
4. Lerdau M., Keller M. Controls on isoprene emission from trees in a subtropical dry forest. Plant Cell Environ. 1997, 20:569-578.
5. Funk J.L., et al. Stress-induced changes in carbon sources for isoprene production in Populus deltoides. Plant Cell Environ. 2004, 27:747-755.
6. Hüve K., et al. Simultaneous growth and emission measurements demonstrate an interactive control of methanol release by leaf expansion and stomata. J. Exp. Bot. 2007, 58:1783-1793.
7. Fall R., Benson A.A. Leaf methanol - the simplest natural product from plants. Trends Plant Sci. 1996, 1:296-301.
8. Cossins E.A. The utilization of carbon-1 compounds from plants. Can. J. Biochem. 1964, 42:1793-1802.
9. Gout E., et al. Metabolism of methanol in plant cells. Carbon-13 nuclear magnetic resonance studies. Plant Physiol. 2000, 123:287-296.
10. Downie A., et al. Expression profiling of the response of Arabidopsis thaliana to methanol stimulation. Phytochemistry 2004, 65:2305-2316.
11. Mirakhori M. Effect of drought stress and methanol on yield and yield components of soybean max (L 17). Am. J. Biochem. Biotechnol. 2009, 5:162.
12. Nonomura A.M., Benson A.A. The path of carbon in photosynthesis: improved crop yields with methanol. Proc. Natl. Acad. Sci. U.S.A. 1992, 89:9794-9798.
13. 12C stable isotopic ratio measurements of methanol emissions give insight into methanol production in Lycopersicon esculentum. New Phytol. 2011, 191:1031-1040.
14. Kreuzwieser J., et al. Interaction of flooding with carbon metabolism of forest trees. Plant Biol. (Stuttg.) 2004, 6:299-306.
15. Kimmerer T.W., Kozlowski T.T. Ethylene, ethane, acetaldehyde, and ethanol production by plants under stress. Plant Physiol. 1982, 69:840-847.
16. Schade G.W., Goldstein A.H. Plant physiological influences on the fluxes of oxygenated volatile organic compounds from ponderosa pine trees. J. Geophys. Res. 2002, 107. ACH 2-1-ACH 2-8.
17. Kreuzwieser J., et al. Metabolic origin of acetaldehyde emitted by poplar (Populus tremula × P. alba) trees. J. Exp. Bot. 1999, 50:757-765.
18. Kreuzwieser J., et al. Acetaldehyde emission by the leaves of Trees - correlation with physiological and environmental parameters. Physiol. Plant. 2001, 113:41-49.
19. Cojocariu C., et al. The effect of ozone on the emission of carbonyls from leaves of adult Fagus sylvatica. Plant Cell Environ. 2005, 28:603-611.
20. Rottenberger S., et al. Exchange of short-chain aldehydes between Amazonian vegetation and the atmosphere. Ecol. Appl. 2004, 14:S247-S262.
21. Jardine K., et al. Plant physiological and environmental controls over the exchange of acetaldehyde between forest canopies and the atmosphere. Biogeosciences 2008, 5:1559-1572.
22. Winters A.J., et al. Emissions of isoprene, monoterpene and short-chained carbonyl compounds from Eucalyptus spp. in southern Australia. Atmos. Environ. 2009, 43:3035-3043.
23. Kesselmeier J., Staudt M. Biogenic volatile organic compounds (VOC): an overview on emission, physiology and ecology. J. Atmos. Chem. 1999, 33:23-88.
24. Holzinger R., et al. Emissions of volatile organic compounds from Quercus ilex L. measured by proton transfer reaction mass spectrometry under different environmental conditions. J. Geophys. Res. Atmos. 2000, 105:20573-20579.
25. Park J-H., et al. Active atmosphere-ecosystem exchange of the vast majority of detected volatile organic compounds. Science 2013, 341:643-647.
26. Falk K.L., et al. Metabolism of monoterpenes in cell cultures of common sage (Salvia officinalis): biochemical rationale for the lack of monoterpene accumulation. Plant Physiol. 1990, 93:1559-1567.
27. Berger R.G., et al. Catabolism of geraniol by cell suspension cultures of Citrus limon. Biochim. Biophys. Acta 1990, 1055:234-239.
28. Croteau R. Biosynthesis and catabolism of monoterpenoids. Chem. Rev. 1987, 87:929-954.
29. Croteau R., Sood V.K. Metabolism of monoterpenes: evidence for the function of monoterpene catabolism in peppermint (Mentha piperita) rhizomes. Plant Physiol. 1985, 77:801-806.
30. Gershenzon J., et al. Regulation of monoterpene accumulation in leaves of peppermint. Plant Physiol. 2000, 122:205-214.
31. Mihaliak C.A., et al. Lack of rapid monoterpene turnover in rooted plants: implications for theories of plant chemical defense. Oecologia 1991, 87:373-376.
32. Mihaliak C.A., Lincoln D.E. Changes in leaf mono- and sesquiterpene metabolism with nitrate availability and leaf age in Heterotheca subaxillaris. J. Chem. Ecol. 1989, 15:1579-1588.
33. Bernard-Dagan C., et al. Biosynthesis of lower terpenoids: genetic and physiological controls in woody plants. Genetic Manipulation of Woody Plants 1988, 329-351. Springer, US. J. Hanover (Ed.).
34. Byers J.A., Birgersson G. Host-tree monoterpenes and biosynthesis of aggregation pheromones in the bark beetle Ips paraconfusus. Psyche 2012, 2012:1-10.
35. Staudt M., Bertin N. Light and temperature dependence of the emission of cyclic and acyclic monoterpenes from holm oak (Quercus ilex L.) leaves. Plant Cell Environ. 1998, 21:385-395.
36. Fall R., Wildermuth M.C. Isoprene synthase: from biochemical mechanism to emission algorithm. J. Geophys. Res. 1998, 103:25599-25609.
37. Jardine K.J., et al. Within-plant isoprene oxidation confirmed by direct emissions of oxidation products methyl vinyl ketone and methacrolein. Global Change Biol. 2012, 18:973-984.
38. Jardine K.J., et al. Emissions of putative isoprene oxidation products from mango branches under abiotic stress. J. Exp. Bot. 2013, 64:3669-3679.
39. Alméras E., et al. Reactive electrophile species activate defense gene expression in Arabidopsis. Plant J. 2003, 34:205-216.
40. Karl T., et al. Efficient atmospheric cleansing of oxidized organic trace gases by vegetation. Science 2010, 330:816-819.
41. Arneth A., et al. Global terrestrial isoprene emission models: sensitivity to variability in climate and vegetation. Atmos. Chem. Phys. 2011, 11:8037-8052.
42. Arneth A., et al. Why are estimates of global terrestrial isoprene emissions so similar (and why is this not so for monoterpenes). Atmos. Chem. Phys. 2008, 8:4605-4620.
43. Seco R., et al. Short-chain oxygenated VOCs: emission and uptake by plants and atmospheric sources, sinks, and concentrations. Atmos. Environ. 2007, 41:2477-2499.
44. Seco R., et al. Formaldehyde emission and uptake by Mediterranean trees Quercus ilex and Pinus halepensis. Atmos. Environ. 2008, 42:7907-7914.
45. Hanson A.D., Roje S. One-carbon metabolism in higher plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 2001, 52:119-137.
46. 2 absorbed by bean and barley leaves from air. Plant Physiol. 1962, 37:833-840.
47. Schmitz H., et al. Assimilation and metabolism of formaldehyde by leaves appear unlikely to be of value for indoor air purification. New Phytol. 2000, 147:307-315.
48. Giese M., et al. Detoxification of formaldehyde by the spider plant (Chlorophytum comosum L.) and by soybean (Glycine max L.) cell-suspension cultures. Plant Physiol. 1994, 104:1301-1309.
49. Kanakidou M., et al. Organic aerosol and global climate modelling: a review. Atmos. Chem. Phys. 2005, 5:1053-1123.
50. Atkinson R., Arey J. Atmospheric chemistry of biogenic organic compounds. Acc. Chem. Res. 1998, 31:574-583.
51. Atkinson R. Atmospheric chemistry of VOCs and NOx. Atmos. Environ. 2000, 34:2063-2101.
52. Lelieveld J., et al. Atmospheric oxidation capacity sustained by a tropical forest. Nature 2008, 452:737-740.
53. Jacob D.J., Wofsy S.C. Photochemistry of biogenic emissions over the Amazon forest. J. Geophys. Res. 1988, 93:1477-1486.
54. McFrederick Q., et al. Effects of air pollution on biogenic volatiles and ecological interactions. Oecologia 2009, 160:411-420.
55. Solomon S., et al. IPCC, 2007: Climate Change 2007: The Physical Science Basis 2007, Cambridge University Press.
56. Guenther A., et al. Estimates of global terrestrial isoprene emissions using MEGAN (Model of Emissions of Gases and Aerosols from Nature). Atmos. Chem. Phys. 2006, 6:3181-3210.
57. Singh H.B., et al. High-concentrations and photochemical fate of oxygenated hydrocarbons in the global troposphere. Nature 1995, 378:50-54.
58. Wesely M.L., Hicks B.B. A review of the current status of knowledge on dry deposition. Atmos. Environ. 2000, 34:2261-2282.
59. Kesselmeier J., et al. Exchange of atmospheric formic and acetic acids with trees and crop plants under controlled chamber and purified air conditions. Atmos. Environ. 1998, 32:1765-1775.
60. Choh Y., et al. Exposure of lima bean leaves to volatiles from herbivore-induced conspecific plants results in emission of carnivore attractants: active or passive process?. J. Chem. Ecol. 2004, 30:1305-1317.
61. Himanen S.J., et al. Birch (Betula spp.) leaves adsorb and re-release volatiles specific to neighbouring plants - a mechanism for associational herbivore resistance?. New Phytol. 2010, 186:722-732.
62. Matsui K., et al. Differential metabolisms of green leaf volatiles in injured and intact parts of a wounded leaf meet distinct ecophysiological requirements. PLoS ONE 2012, 7:e36433.
63. Farag M.A., et al. (Z)-3-Hexenol induces defense genes and downstream metabolites in maize. Planta 2005, 220:900-909.
64. Frost C.J., et al. Priming defense genes and metabolites in hybrid poplar by the green leaf volatile cis-3-hexenyl acetate. New Phytol. 2008, 180:722-733.
65. Heil M., Silva Bueno J.C. Within-plant signaling by volatiles leads to induction and priming of an indirect plant defense in nature. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:5467-5472.
66. Lin Z., et al. Recent advances in ethylene research. J. Exp. Bot. 2009, 60:3311-3336.
67. Holopainen J., Blande J. Molecular plant volatile communication. Sensing in Nature 2012, 17-31. Springer, US. C. López-Larrea (Ed.).
68. Terry G.M., et al. Exposure to isoprene promotes flowering in plants. J. Exp. Bot. 1995, 46:1629-1631.
69. Kessler A., et al. Priming of plant defense responses in nature by airborne signaling between Artemisia tridentata and Nicotiana attenuata. Oecologia 2006, 148:280-292.
70. Blande J.D., et al. Air pollution impedes plant-to-plant communication by volatiles. Ecol. Lett. 2010, 13:1172-1181.
71. McFrederick Q.S., et al. Air pollution modifies floral scent trails. Atmos. Environ. 2008, 42:2336-2348.
72. Fuentes J.D., et al. Ozone impedes the ability of a herbivore to find its host. Environ. Res. Lett. 2013, 8:014048.
73. 3) polluted atmospheres: the ecological effects. J. Chem. Ecol. 2010, 36:22-34.
74. Arndt U. Air-pollutants and pheromones - a problem. Chemosphere 1995, 30:1023-1031.
75. Ferrieri R.A., et al. Use of carbon-11 in Populus shows that exogenous jasmonic acid increases biosynthesis of isoprene from recently fixed carbon. Plant Cell Environ. 2005, 28:591-602.
76. Hourton-Cabassa C., et al. Stress induction of mitochondrial formate dehydrogenase in potato leaves. Plant Physiol. 1998, 116:627-635.
77. Guenther A., et al. Natural emissions of non-methane volatile organic compounds; carbon monoxide, and oxides of nitrogen from North America. Atmos. Environ. 2000, 34:2205-2230.
78. Millet D.B., et al. Global atmospheric budget of acetaldehyde: 3-D model analysis and constraints from in-situ and satellite observations. Atmos. Chem. Phys. 2010, 10:3405-3425.
79. Guenther A.B., et al. Isoprene and monoterpene emission rate variability - model evaluations and sensitivity analyses. J. Geophys. Res. 1993, 98:12609-12617.
80. Galbally I.E., Kirstine W. The production of methanol by flowering plants and the global cycle of methanol. J. Atmos. Chem. 2002, 43:195-229.