The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves
Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in...
Ausführliche Beschreibung
Autor*in: |
Krome, K. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2007 |
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Anmerkung: |
© Deutsche Phythomedizinische Gesellschaft 2007 |
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Übergeordnetes Werk: |
Enthalten in: Journal of plant diseases and protection - Berlin : Springer, 2006, 114(2007), 6 vom: Dez., Seite 250-255 |
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Übergeordnetes Werk: |
volume:114 ; year:2007 ; number:6 ; month:12 ; pages:250-255 |
Links: |
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DOI / URN: |
10.1007/BF03356225 |
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Katalog-ID: |
SPR038183773 |
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245 | 1 | 4 | |a The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
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520 | |a Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. | ||
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700 | 1 | |a Aumann, J. |4 aut | |
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10.1007/BF03356225 doi (DE-627)SPR038183773 (SPR)BF03356225-e DE-627 ger DE-627 rakwb eng Krome, K. verfasserin aut The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phythomedizinische Gesellschaft 2007 Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. Kabsch, U. aut Aumann, J. aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 114(2007), 6 vom: Dez., Seite 250-255 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:114 year:2007 number:6 month:12 pages:250-255 https://dx.doi.org/10.1007/BF03356225 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_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_374 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_2018 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_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 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_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 114 2007 6 12 250-255 |
spelling |
10.1007/BF03356225 doi (DE-627)SPR038183773 (SPR)BF03356225-e DE-627 ger DE-627 rakwb eng Krome, K. verfasserin aut The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phythomedizinische Gesellschaft 2007 Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. Kabsch, U. aut Aumann, J. aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 114(2007), 6 vom: Dez., Seite 250-255 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:114 year:2007 number:6 month:12 pages:250-255 https://dx.doi.org/10.1007/BF03356225 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_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_374 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_2018 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_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 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_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 114 2007 6 12 250-255 |
allfields_unstemmed |
10.1007/BF03356225 doi (DE-627)SPR038183773 (SPR)BF03356225-e DE-627 ger DE-627 rakwb eng Krome, K. verfasserin aut The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phythomedizinische Gesellschaft 2007 Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. Kabsch, U. aut Aumann, J. aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 114(2007), 6 vom: Dez., Seite 250-255 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:114 year:2007 number:6 month:12 pages:250-255 https://dx.doi.org/10.1007/BF03356225 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_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_374 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_2018 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_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 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_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 114 2007 6 12 250-255 |
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10.1007/BF03356225 doi (DE-627)SPR038183773 (SPR)BF03356225-e DE-627 ger DE-627 rakwb eng Krome, K. verfasserin aut The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phythomedizinische Gesellschaft 2007 Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. Kabsch, U. aut Aumann, J. aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 114(2007), 6 vom: Dez., Seite 250-255 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:114 year:2007 number:6 month:12 pages:250-255 https://dx.doi.org/10.1007/BF03356225 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_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_374 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_2018 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_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 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_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 114 2007 6 12 250-255 |
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10.1007/BF03356225 doi (DE-627)SPR038183773 (SPR)BF03356225-e DE-627 ger DE-627 rakwb eng Krome, K. verfasserin aut The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves 2007 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Deutsche Phythomedizinische Gesellschaft 2007 Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. Kabsch, U. aut Aumann, J. aut Enthalten in Journal of plant diseases and protection Berlin : Springer, 2006 114(2007), 6 vom: Dez., Seite 250-255 (DE-627)508335310 (DE-600)2224048-2 1861-3837 nnns volume:114 year:2007 number:6 month:12 pages:250-255 https://dx.doi.org/10.1007/BF03356225 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_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_374 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_2018 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_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 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_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 AR 114 2007 6 12 250-255 |
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Krome, K. |
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Krome, K. The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
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The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
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The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
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The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
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Krome, K. |
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Krome, K. Kabsch, U. Aumann, J. |
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title_sort |
effect of benzothiadiazole and fungal extracts of cercospora beticola and fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
title_auth |
The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
abstract |
Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. © Deutsche Phythomedizinische Gesellschaft 2007 |
abstractGer |
Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. © Deutsche Phythomedizinische Gesellschaft 2007 |
abstract_unstemmed |
Abstract The cytosolic phosphoenolpyruvate carboxylase (PEPC) catalyses the anaplerotic synthesis of oxalacetic acid resulting in the replenishment of citric acid cycle intermediates, which are precursors for the synthesis of amino acids. Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants. © Deutsche Phythomedizinische Gesellschaft 2007 |
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container_issue |
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title_short |
The effect of benzothiadiazole and fungal extracts of Cercospora beticola and Fusarium graminearum on phosphoenolpyruvate carboxylase activity in cucumber leaves |
url |
https://dx.doi.org/10.1007/BF03356225 |
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Biotic stress in plants generally leads to redistributions in primary and secondary pathways and therefore to a shift in the requirement of proteins. To reveal whether and how PEPC is affected by biotic stress we analysed PEPC activity after treating cucumber (Cucumis sativus) leaves with the synthetic plant activator benzothiadiazole (BTH) and extracts of the economically important phytopathogenic fungi Cercospora beticola and Fusarium graminearum. BTH as well as fungal extracts increased PEPC activity significantly 72 and 96 hours after treatments. In addition, the extracts, but not BTH, induced the formation of necrotic lesions. Defence responses are generally associated with decreased photosynthesis rates, an enhanced respiration rate and an increased demand in proteins. Regarding our results we assume that the increase in PEPC activity by biotic stress is conducive to a compensation of these antagonistic processes. However, PEPC activity enhancements are not necessarily associated with the formation of necrotic lesions. This study indicates that PEPC is involved in biotic stress responses and we suggest that PEPC contributes to successful defence responses in plants.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kabsch, U.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Aumann, J.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of plant diseases and protection</subfield><subfield code="d">Berlin : Springer, 2006</subfield><subfield code="g">114(2007), 6 vom: Dez., Seite 250-255</subfield><subfield code="w">(DE-627)508335310</subfield><subfield code="w">(DE-600)2224048-2</subfield><subfield code="x">1861-3837</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:114</subfield><subfield code="g">year:2007</subfield><subfield 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