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Relevant bibliographies by topics / Protoporphyrinogen inhibitor

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Academic literature on the topic 'Protoporphyrinogen inhibitor'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Protoporphyrinogen inhibitor"

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Ferreira, G. C., and H. A. Dailey. "Mouse protoporphyrinogen oxidase. Kinetic parameters and demonstration of inhibition by bilirubin." Biochemical Journal 250, no. 2 (1988): 597–603. http://dx.doi.org/10.1042/bj2500597.

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The penultimate step of haem biosynthesis, the oxidation of protoporphyrinogen to protoporphyrin, was examined with purified murine hepatic protoporphyrinogen oxidase (EC 1.3.3.4) in detergent solution. The kinetic parameters for the two-substrate (protoporphyrinogen and oxygen) reaction were determined. The limiting Km for protoporphyrinogen when oxygen is saturating is 6.6 microM, whereas the Km for oxygen with saturating concentrations of protoporphyrinogen is 125 microM. The kcat. for the overall reaction is 447 h-1. The ratio of kcat. to the Km for protoporphyrinogen is approx. 20-fold gr

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Hao, Ge-Fei, Yang Zuo, Sheng-Gang Yang, and Guang-Fu Yang. "Protoporphyrinogen Oxidase Inhibitor: An Ideal Target for Herbicide Discovery." CHIMIA International Journal for Chemistry 65, no. 12 (2011): 961–69. http://dx.doi.org/10.2533/chimia.2011.961.

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Wright, Terry R., E. Patrick Fuerst, Alex G. Ogg, Ujjana B. Nandihalli, and Hee Jae Lee. "Herbicidal Activity of UCC-C4243 and Acifluorfen is Due to Inhibition of Protoporphyrinogen Oxidase." Weed Science 43, no. 1 (1995): 47–54. http://dx.doi.org/10.1017/s0043174500080814.

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Laboratory and greenhouse studies were conducted to determine the mode of action of soil- and foliar-applied UCC-C4243. Experiments demonstrated that UCC-C4243 required light for phytotoxicity, phytotoxic symptoms were similar to inhibitors of porphyrin synthesis such as acifluorfen, and UCC-C4243 potently inhibited protoporphyrinogen oxidase. Germination and emergence of field pennycress and lentil in the dark were not affected by soil-incorporated UCC-C4243 at rates more than 10 times greater than like treatments that killed all plants in the light. Soil-incorporated UCC-C4243 required light

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Jung, Ha Il, and Yong In Kuk. "Resistance mechanisms in protoporphyrinogen oxidase (PROTOX) inhibitor-resistant transgenic rice." Journal of Plant Biology 50, no. 5 (2007): 586–94. http://dx.doi.org/10.1007/bf03030713.

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Daugrois, J. H., J. W. Hoy, and J. L. Griffin. "Protoporphyrinogen Oxidase Inhibitor Herbicide Effects on Pythium Root Rot of Sugarcane, Pythium Species, and the Soil Microbial Community." Phytopathology® 95, no. 3 (2005): 220–26. http://dx.doi.org/10.1094/phyto-95-0220.

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The effects of three protoporphyrinogen oxidase inhibitor herbicides, azafenidin, flumioxazin, and sulfentrazone, on Pythium root rot of sugarcane and the soil microbial community were evaluated in greenhouse experiments. Herbicides were applied as foliar and soil treatments. There were no consistent effects on plant growth or disease parameters. However, some herbicide treatments affected the relative frequency of isolation of Pythium spp. from roots and reduced colonization by the pathogenic species Pythium arrhenomanes. A comparison of sole carbon source utilization profiles indicated that

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Falk, Jeanne S., Kassim Al-Khatib, and Dallas E. Peterson. "Rapid Assay Evaluation of Plant Response to Protoporphyrinogen Oxidase (Protox)-Inhibiting Herbicides." Weed Technology 20, no. 1 (2006): 104–12. http://dx.doi.org/10.1614/wt-04-302r.1.

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Protoporphyrinogen oxidase (protox)-inhibiting herbicides damage cell membranes, resulting in electrolyte leakage. A whole-plant dose-response study and a rapid assay that measured electrolyte leakage was used to determine the response of wild mustard, soybean, and protox inhibitor–susceptible and protox inhibitor–resistant common waterhemp to increasing doses of three protox inhibitors: acifluorfen, fomesafen, and sulfentrazone. For the dose-response study, whole plants were treated with the three protox-inhibitor herbicides. Electroconductivity assay 1 consisted of cutting discs from leaf ti

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BRUSAMARELLO, A. P., P. H. OLIVEIRA, M. M. TREZZI, E. XAVIER, and E. D. DALOSTO. "INHERITANCE OF RESISTANCE TO PROTOPORPHYRINOGEN OXIDASE INHIBITOR HERBICIDES IN WILD POINSETTIA." Planta Daninha 34, no. 3 (2016): 575–80. http://dx.doi.org/10.1590/s0100-83582016340300018.

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ABSTRACT Weed resistance to herbicides is a major global problem for agriculture. In recent years, the increased use of herbicides, without proper planning, has led to a large increase in the number of cases of weed biotypes that are resistant to one or more herbicide mechanism of action. Wild poinsettia biotypes (Euphorbia heterophylla), discovered in the State of Paraná, with resistance to herbicides that inhibit protoporphyrinogen oxidase (PROTOX) and acetolactate synthase (ALS), are the first case to exhibit multiple resistance in Brazil. This study analyzed the genetic inheritance of PROT

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Beckie, Hugh J., Eric N. Johnson, and Anne Légère. "Negative Cross-Resistance of Acetolactate Synthase Inhibitor–Resistant Kochia (Kochia scoparia) to Protoporphyrinogen Oxidase– and Hydroxyphenylpyruvate Dioxygenase–Inhibiting Herbicides." Weed Technology 26, no. 3 (2012): 570–74. http://dx.doi.org/10.1614/wt-d-12-00020.1.

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This greenhouse experiment examined the response of homozygous susceptible and acetolactate synthase (ALS) inhibitor–resistant plants from six Canadian kochia accessions with the Pro197 or Trp574 mutation to six alternative herbicides of different sites of action. The null hypothesis was ALS-inhibitor–resistant and –susceptible plants from within and across accessions would respond similarly to herbicides of different sites of action. This hypothesis was accepted for all accessions except that of MBK2 with the Trp574 mutation. Resistant plants of that accession were 80, 60, and 50% more sensit

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Cahoon, Charles W., Alan C. York, David L. Jordan, Wesley J. Everman, and Richard W. Seagroves. "An Alternative to Multiple Protoporphyrinogen Oxidase Inhibitor Applications in No-Till Cotton." Weed Technology 28, no. 1 (2014): 58–71. http://dx.doi.org/10.1614/wt-d-13-00078.1.

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Glyphosate-resistant (GR) Palmer amaranth is a widespread problem in southeastern cotton production areas. Herbicide programs to control this weed in no-till cotton commonly include flumioxazin applied with preplant burndown herbicides approximately 3 wk before planting followed by fomesafen applied PRE and then glufosinate or glyphosate applied POST. Flumioxazin and fomesafen are both protoporphyrinogen oxidase (PPO) inhibitors. Multiple yearly applications of PPO inhibitors in cotton, along with widespread use of PPO inhibitors in rotational crops, raise concerns over possible selection for

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Umphres, Alinna M., Lawrence E. Steckel, and Thomas C. Mueller. "Control of Protoporphyrinogen Oxidase Inhibiting Herbicide Resistant and Susceptible Palmer Amaranth (Amaranthus palmeri) with Soil-Applied Protoporphyrinogen Oxidase–Inhibiting Herbicides." Weed Technology 32, no. 1 (2017): 95–100. http://dx.doi.org/10.1017/wet.2017.78.

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AbstractPalmer amaranth resistance to protoporphyrinogen oxidase (PPO)-inhibiting herbicides has become an increasing problem to producers throughout the southeast region of the United States. Traditionally, these herbicides can be used as foliar-applied and soil-applied in glyphosate resistant (GR) cropping systems to control GR Palmer amaranth. Heavy reliance on PPO herbicides has contributed to the increased selection for PPO inhibitor-resistant (PPO-R) Palmer amaranth biotypes. Dose response greenhouse research was conducted to evaluate the efficacy of soil-applied flumioxazin, fomesafen,

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Dissertations / Theses on the topic "Protoporphyrinogen inhibitor"

1

Gitsopoulos, Thomas. "Studies on the biology and chemical control of barnyardgrass (Echinochloa crus-galli) in rice (Oryza sativa) with the herbicide oxadiargyl." Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325205.

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Book chapters on the topic "Protoporphyrinogen inhibitor"

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Theodoridis, George, Rex Liebl, and Cyrill Zagar. "Protoporphyrinogen IX Oxidase Inhibitors." In Modern Crop Protection Compounds. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527644179.ch3.

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Zagar, Cyrill, Rex Liebl, George Theodoridis, and Matthias Witschel. "Protoporphyrinogen IX Oxidase Inhibitors." In Modern Crop Protection Compounds. Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527699261.ch3.

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Clark, Robert D. "Synthesis of Protoporphyrinogen Oxidase Inhibitors." In Porphyric Pesticides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0559.ch003.

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Halling, B. P., D. A. Yuhas, V. F. Fingar, and J. W. Winkelmann. "Protoporphyrinogen Oxidase Inhibitors for Tumor Therapy." In Porphyric Pesticides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0559.ch020.

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Nagano, Eiki. "Herbicidal Efficacy of Protoporphyrinogen Oxidase Inhibitors." In Peroxidizing Herbicides. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-58633-0_11.

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Matsumoto, Hiroshi. "Inhibitors of Protoporphyrinogen Oxidase: A Brief Update." In Herbicide Classes in Development. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-59416-8_8.

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Matsumoto, H., J. J. Lee, and K. Ishizuka. "Variation in Crop Response to Protoporphyrinogen Oxidase Inhibitors." In Porphyric Pesticides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0559.ch009.

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Krijt, J., M. Vokurka, J. Sanitrák, and V. Janousek. "Effect of Protoporphyrinogen Oxidase Inhibitors on Mammalian Porphyrin Metabolism." In Porphyric Pesticides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0559.ch017.

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Sato, Ryo, Masako Yamamoto, Hideyuki Shibata, et al. "Characterization of a Mutant ofChlamydomonas reinhardtiiResistant to Protoporphyrinogen Oxidase Inhibitors." In Porphyric Pesticides. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0559.ch007.

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Reddy, Krishna N., Ujjana B. Nandihalli, Hee Jae Lee, Mary V. Duke, and Stephen O. Duke. "Predicting Activity of Protoporphyrinogen Oxidase Inhibitors by Computer-Aided Molecular Modeling." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0589.ch015.

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