Nitric oxide synthase-like protein in pea (Pisum sativum L.)
Nitric oxide synthase activity was detected in pea (Pisum sativum L.) leaf extracts using a citrulline formation assay that is typically employed in mammalian systems. A total protein extraction method was modified from that used in mammalian systems based on biochemical activities such as the use o...
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Wiley-VCH Verlag GmbH & Co. KGaA
2010
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Online Access: | http://psasir.upm.edu.my/id/eprint/51943/1/Nitric%20oxide%20synthase-like%20protein%20in%20pea%20%28Pisum%20sativum%20L.%29.pdf http://psasir.upm.edu.my/id/eprint/51943/ http://onlinelibrary.wiley.com/doi/10.1002/9783527629138.ch12/summary |
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my.upm.eprints.519432017-05-04T04:26:24Z http://psasir.upm.edu.my/id/eprint/51943/ Nitric oxide synthase-like protein in pea (Pisum sativum L.) Wong, Mui Yun Huang, Jeng Sheng Davis, Eric L. Sukno, Serenella Tan, Yee How Nitric oxide synthase activity was detected in pea (Pisum sativum L.) leaf extracts using a citrulline formation assay that is typically employed in mammalian systems. A total protein extraction method was modified from that used in mammalian systems based on biochemical activities such as the use of protease inhibitors, pH, and precipitation with salts and organic solvents. Physiological aspects in plants, such as effects of chemicals that induce systemic resistance to NOS activity and immunodetection of an NOS-like protein, were also studied. The NOS-like protein was partially isolated using liquid chromatography and characterized based on mammalian NOS inhibitor and cofactor requirements. Correlation of NOS activity and NOS-like gene expression during incompatible and compatible pea–bacteria interactions were investigated using interactions of Ralstonia solanacearum and Pseudomonas syringae pv. pisi, respectively, with pea. NOS activity was detected using citrulline formation assay. Gene expression was measured using real-time reverse transcription-polymerase chain reactions and a 348-bp probe designed from a cloned cDNA fragment of pea that was homologous to NOS of snail and AtNOS1/AtNOA1 of Arabidopsis. The possibility of NO production from various sources in cells of pea is also discussed. Wiley-VCH Verlag GmbH & Co. KGaA Hayat, Shamsul Mori, Masaki Pichtel, John Ahmad, Aqil 2010 Book Section PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/51943/1/Nitric%20oxide%20synthase-like%20protein%20in%20pea%20%28Pisum%20sativum%20L.%29.pdf Wong, Mui Yun and Huang, Jeng Sheng and Davis, Eric L. and Sukno, Serenella and Tan, Yee How (2010) Nitric oxide synthase-like protein in pea (Pisum sativum L.). In: Nitric Oxide in Plant Physiology. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, pp. 173-188. ISBN 9783527325191; EISBN: 9783527629138 http://onlinelibrary.wiley.com/doi/10.1002/9783527629138.ch12/summary 10.1002/9783527629138.ch12 |
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Nitric oxide synthase activity was detected in pea (Pisum sativum L.) leaf extracts using a citrulline formation assay that is typically employed in mammalian systems. A total protein extraction method was modified from that used in mammalian systems based on biochemical activities such as the use of protease inhibitors, pH, and precipitation with salts and organic solvents. Physiological aspects in plants, such as effects of chemicals that induce systemic resistance to NOS activity and immunodetection of an NOS-like protein, were also studied. The NOS-like protein was partially isolated using liquid chromatography and characterized based on mammalian NOS inhibitor and cofactor requirements. Correlation of NOS activity and NOS-like gene expression during incompatible and compatible pea–bacteria interactions were investigated using interactions of Ralstonia solanacearum and Pseudomonas syringae pv. pisi, respectively, with pea. NOS activity was detected using citrulline formation assay. Gene expression was measured using real-time reverse transcription-polymerase chain reactions and a 348-bp probe designed from a cloned cDNA fragment of pea that was homologous to NOS of snail and AtNOS1/AtNOA1 of Arabidopsis. The possibility of NO production from various sources in cells of pea is also discussed. |
author2 |
Hayat, Shamsul |
author_facet |
Hayat, Shamsul Wong, Mui Yun Huang, Jeng Sheng Davis, Eric L. Sukno, Serenella Tan, Yee How |
format |
Book Section |
author |
Wong, Mui Yun Huang, Jeng Sheng Davis, Eric L. Sukno, Serenella Tan, Yee How |
spellingShingle |
Wong, Mui Yun Huang, Jeng Sheng Davis, Eric L. Sukno, Serenella Tan, Yee How Nitric oxide synthase-like protein in pea (Pisum sativum L.) |
author_sort |
Wong, Mui Yun |
title |
Nitric oxide synthase-like protein in pea (Pisum sativum L.) |
title_short |
Nitric oxide synthase-like protein in pea (Pisum sativum L.) |
title_full |
Nitric oxide synthase-like protein in pea (Pisum sativum L.) |
title_fullStr |
Nitric oxide synthase-like protein in pea (Pisum sativum L.) |
title_full_unstemmed |
Nitric oxide synthase-like protein in pea (Pisum sativum L.) |
title_sort |
nitric oxide synthase-like protein in pea (pisum sativum l.) |
publisher |
Wiley-VCH Verlag GmbH & Co. KGaA |
publishDate |
2010 |
url |
http://psasir.upm.edu.my/id/eprint/51943/1/Nitric%20oxide%20synthase-like%20protein%20in%20pea%20%28Pisum%20sativum%20L.%29.pdf http://psasir.upm.edu.my/id/eprint/51943/ http://onlinelibrary.wiley.com/doi/10.1002/9783527629138.ch12/summary |
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1643835102254333952 |
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13.18916 |