Roles of reactive oxygen species in interactions between plants and pathogens

Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Shetty, Nandini P. [verfasserIn] Jørgensen, Hans J. Lyngs [verfasserIn] Jensen, Jens Due [verfasserIn] Collinge, David B. [verfasserIn] Shetty, H. Shekar [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2008

Schlagwörter:	Antimicrobial Cell wall cross-linking Hypersensitive response Signal transduction Gene expression Successful pathogenesis Hydrogen peroxide

Übergeordnetes Werk:	Enthalten in: European journal of plant pathology - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1895, 121(2008), 3 vom: 20. Mai, Seite 267-280
Übergeordnetes Werk:	volume:121 ; year:2008 ; number:3 ; day:20 ; month:05 ; pages:267-280

Links:	Volltext

DOI / URN:	10.1007/s10658-008-9302-5

Katalog-ID:	SPR012162841

Internformat


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520			\|a Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens.
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700	1		\|a Shetty, H. Shekar \|e verfasserin \|4 aut
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912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_152
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_171
912			\|a GBV_ILN_187
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_250
912			\|a GBV_ILN_281
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
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912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2031
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2039
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2057
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2065
912			\|a GBV_ILN_2068
912			\|a GBV_ILN_2070
912			\|a GBV_ILN_2086
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2093
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2107
912			\|a GBV_ILN_2108
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2113
912			\|a GBV_ILN_2118
912			\|a GBV_ILN_2119
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2144
912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
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912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
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912			\|a GBV_ILN_4313
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912			\|a GBV_ILN_4334
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matchkey_str	article:15738469:2008----::oeoratvoyeseisnneatosewe
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publishDate	2008
allfields	10.1007/s10658-008-9302-5 doi (DE-627)SPR012162841 (SPR)s10658-008-9302-5-e DE-627 ger DE-627 rakwb eng 580 630 640 ASE 48.54 bkl Shetty, Nandini P. verfasserin aut Roles of reactive oxygen species in interactions between plants and pathogens 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens. Antimicrobial (dpeaa)DE-He213 Cell wall cross-linking (dpeaa)DE-He213 Hypersensitive response (dpeaa)DE-He213 Signal transduction (dpeaa)DE-He213 Gene expression (dpeaa)DE-He213 Successful pathogenesis (dpeaa)DE-He213 Hydrogen peroxide (dpeaa)DE-He213 Jørgensen, Hans J. Lyngs verfasserin aut Jensen, Jens Due verfasserin aut Collinge, David B. verfasserin aut Shetty, H. Shekar verfasserin aut Enthalten in European journal of plant pathology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1895 121(2008), 3 vom: 20. Mai, Seite 267-280 (DE-627)27042976X (DE-600)1477679-0 1573-8469 nnns volume:121 year:2008 number:3 day:20 month:05 pages:267-280 https://dx.doi.org/10.1007/s10658-008-9302-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 48.54 ASE AR 121 2008 3 20 05 267-280
spelling	10.1007/s10658-008-9302-5 doi (DE-627)SPR012162841 (SPR)s10658-008-9302-5-e DE-627 ger DE-627 rakwb eng 580 630 640 ASE 48.54 bkl Shetty, Nandini P. verfasserin aut Roles of reactive oxygen species in interactions between plants and pathogens 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens. Antimicrobial (dpeaa)DE-He213 Cell wall cross-linking (dpeaa)DE-He213 Hypersensitive response (dpeaa)DE-He213 Signal transduction (dpeaa)DE-He213 Gene expression (dpeaa)DE-He213 Successful pathogenesis (dpeaa)DE-He213 Hydrogen peroxide (dpeaa)DE-He213 Jørgensen, Hans J. Lyngs verfasserin aut Jensen, Jens Due verfasserin aut Collinge, David B. verfasserin aut Shetty, H. Shekar verfasserin aut Enthalten in European journal of plant pathology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1895 121(2008), 3 vom: 20. Mai, Seite 267-280 (DE-627)27042976X (DE-600)1477679-0 1573-8469 nnns volume:121 year:2008 number:3 day:20 month:05 pages:267-280 https://dx.doi.org/10.1007/s10658-008-9302-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 48.54 ASE AR 121 2008 3 20 05 267-280
allfields_unstemmed	10.1007/s10658-008-9302-5 doi (DE-627)SPR012162841 (SPR)s10658-008-9302-5-e DE-627 ger DE-627 rakwb eng 580 630 640 ASE 48.54 bkl Shetty, Nandini P. verfasserin aut Roles of reactive oxygen species in interactions between plants and pathogens 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens. Antimicrobial (dpeaa)DE-He213 Cell wall cross-linking (dpeaa)DE-He213 Hypersensitive response (dpeaa)DE-He213 Signal transduction (dpeaa)DE-He213 Gene expression (dpeaa)DE-He213 Successful pathogenesis (dpeaa)DE-He213 Hydrogen peroxide (dpeaa)DE-He213 Jørgensen, Hans J. Lyngs verfasserin aut Jensen, Jens Due verfasserin aut Collinge, David B. verfasserin aut Shetty, H. Shekar verfasserin aut Enthalten in European journal of plant pathology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1895 121(2008), 3 vom: 20. Mai, Seite 267-280 (DE-627)27042976X (DE-600)1477679-0 1573-8469 nnns volume:121 year:2008 number:3 day:20 month:05 pages:267-280 https://dx.doi.org/10.1007/s10658-008-9302-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 48.54 ASE AR 121 2008 3 20 05 267-280
allfieldsGer	10.1007/s10658-008-9302-5 doi (DE-627)SPR012162841 (SPR)s10658-008-9302-5-e DE-627 ger DE-627 rakwb eng 580 630 640 ASE 48.54 bkl Shetty, Nandini P. verfasserin aut Roles of reactive oxygen species in interactions between plants and pathogens 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens. Antimicrobial (dpeaa)DE-He213 Cell wall cross-linking (dpeaa)DE-He213 Hypersensitive response (dpeaa)DE-He213 Signal transduction (dpeaa)DE-He213 Gene expression (dpeaa)DE-He213 Successful pathogenesis (dpeaa)DE-He213 Hydrogen peroxide (dpeaa)DE-He213 Jørgensen, Hans J. Lyngs verfasserin aut Jensen, Jens Due verfasserin aut Collinge, David B. verfasserin aut Shetty, H. Shekar verfasserin aut Enthalten in European journal of plant pathology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1895 121(2008), 3 vom: 20. Mai, Seite 267-280 (DE-627)27042976X (DE-600)1477679-0 1573-8469 nnns volume:121 year:2008 number:3 day:20 month:05 pages:267-280 https://dx.doi.org/10.1007/s10658-008-9302-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 48.54 ASE AR 121 2008 3 20 05 267-280
allfieldsSound	10.1007/s10658-008-9302-5 doi (DE-627)SPR012162841 (SPR)s10658-008-9302-5-e DE-627 ger DE-627 rakwb eng 580 630 640 ASE 48.54 bkl Shetty, Nandini P. verfasserin aut Roles of reactive oxygen species in interactions between plants and pathogens 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens. Antimicrobial (dpeaa)DE-He213 Cell wall cross-linking (dpeaa)DE-He213 Hypersensitive response (dpeaa)DE-He213 Signal transduction (dpeaa)DE-He213 Gene expression (dpeaa)DE-He213 Successful pathogenesis (dpeaa)DE-He213 Hydrogen peroxide (dpeaa)DE-He213 Jørgensen, Hans J. Lyngs verfasserin aut Jensen, Jens Due verfasserin aut Collinge, David B. verfasserin aut Shetty, H. Shekar verfasserin aut Enthalten in European journal of plant pathology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1895 121(2008), 3 vom: 20. Mai, Seite 267-280 (DE-627)27042976X (DE-600)1477679-0 1573-8469 nnns volume:121 year:2008 number:3 day:20 month:05 pages:267-280 https://dx.doi.org/10.1007/s10658-008-9302-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 48.54 ASE AR 121 2008 3 20 05 267-280
language	English
source	Enthalten in European journal of plant pathology 121(2008), 3 vom: 20. Mai, Seite 267-280 volume:121 year:2008 number:3 day:20 month:05 pages:267-280
sourceStr	Enthalten in European journal of plant pathology 121(2008), 3 vom: 20. Mai, Seite 267-280 volume:121 year:2008 number:3 day:20 month:05 pages:267-280
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Antimicrobial Cell wall cross-linking Hypersensitive response Signal transduction Gene expression Successful pathogenesis Hydrogen peroxide
dewey-raw	580
isfreeaccess_bool	false
container_title	European journal of plant pathology
authorswithroles_txt_mv	Shetty, Nandini P. @@aut@@ Jørgensen, Hans J. Lyngs @@aut@@ Jensen, Jens Due @@aut@@ Collinge, David B. @@aut@@ Shetty, H. Shekar @@aut@@
publishDateDaySort_date	2008-05-20T00:00:00Z
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language_de	englisch
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author	Shetty, Nandini P.
spellingShingle	Shetty, Nandini P. ddc 580 bkl 48.54 misc Antimicrobial misc Cell wall cross-linking misc Hypersensitive response misc Signal transduction misc Gene expression misc Successful pathogenesis misc Hydrogen peroxide Roles of reactive oxygen species in interactions between plants and pathogens
authorStr	Shetty, Nandini P.
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topic_title	580 630 640 ASE 48.54 bkl Roles of reactive oxygen species in interactions between plants and pathogens Antimicrobial (dpeaa)DE-He213 Cell wall cross-linking (dpeaa)DE-He213 Hypersensitive response (dpeaa)DE-He213 Signal transduction (dpeaa)DE-He213 Gene expression (dpeaa)DE-He213 Successful pathogenesis (dpeaa)DE-He213 Hydrogen peroxide (dpeaa)DE-He213
topic	ddc 580 bkl 48.54 misc Antimicrobial misc Cell wall cross-linking misc Hypersensitive response misc Signal transduction misc Gene expression misc Successful pathogenesis misc Hydrogen peroxide
topic_unstemmed	ddc 580 bkl 48.54 misc Antimicrobial misc Cell wall cross-linking misc Hypersensitive response misc Signal transduction misc Gene expression misc Successful pathogenesis misc Hydrogen peroxide
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title_full	Roles of reactive oxygen species in interactions between plants and pathogens
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author-letter	Shetty, Nandini P.
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title_sort	roles of reactive oxygen species in interactions between plants and pathogens
title_auth	Roles of reactive oxygen species in interactions between plants and pathogens
abstract	Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens.
abstractGer	Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens.
abstract_unstemmed	Abstract The production of reactive oxygen species (ROS) by the consumption of molecular oxygen during host–pathogen interactions is termed the oxidative burst. The most important ROS are singlet oxygen (1$ O_{2} $), the hydroxyperoxyl radical ($ HO_{2} $·), the superoxide anion %$\left( {{\text{O}}_{\text{2}} ^ - } \right)%$, hydrogen peroxide ($ H_{2} %$ O_{2} $), the hydroxyl radical ($ OH^{-} $) and the closely related reactive nitrogen species, nitric oxide (NO). These ROS are highly reactive, and therefore toxic, and participate in several important processes related to defence and infection. Furthermore, ROS also play important roles in plant biology both as toxic by-products of aerobic metabolism and as key regulators of growth, development and defence pathways. In this review, we will assess the different roles of ROS in host–pathogen interactions with special emphasis on fungal and Oomycete pathogens.
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container_issue	3
title_short	Roles of reactive oxygen species in interactions between plants and pathogens
url	https://dx.doi.org/10.1007/s10658-008-9302-5
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author2	Jørgensen, Hans J. Lyngs Jensen, Jens Due Collinge, David B. Shetty, H. Shekar
author2Str	Jørgensen, Hans J. Lyngs Jensen, Jens Due Collinge, David B. Shetty, H. Shekar
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doi_str	10.1007/s10658-008-9302-5
up_date	2024-07-04T02:02:37.685Z
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Roles of reactive oxygen species in interactions between plants and pathogens

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