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Myrsinoic A acid and its derivative: in vitro inhibitors of photosynthesis; Acido myrsinoico A e derivado: inibidores da fotossintese in vitro

Abstract

Myrsinoic A acid, isolated from Myrsine cuneifolia and its hydrogenated derivative had their effect on photosynthesis tested. The compounds inhibited the electron flow (basal, phosphorylating and uncoupled) from water to methyl viologen; therefore, they act as Hill reaction inhibitors in spinach thylakoids. They inhibited partial reactions of PSII electron flow from water to 2,5-dichloro-1,4-benzoquinone, from water to sodium silicomolybdate, and partially electron flow from diphenylcarbazide to 2,6-dichloroindophenol. Their inhibition sites were at the donor and acceptor sides of PSII, between P{sub 680} and Q{sub A}. Chlorophyll {alpha} fluorescence measurements confirmed the behavior of the compounds (pool of quinones). (author)
Authors:
Burger, Marcela Carmen de M.; Oliveira, Gracielle S. de; Menezes, Antonio Carlos S; [1]  Vieira, Paulo Cezar; Silva, Maria Fatima das G.F. da; [2]  Veiga, Thiago A.M., E-mail: tveiga@unifesp.br [3] 
  1. Universidade Estadual de Goias, Anapolis, GO (Brazil). Unidade Universitaria de Ciencias Exatas e Tecnologicas
  2. Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Dept. de Quimica
  3. Universidade Federal de Sao Paulo (UNIFESP), SP (Brazil). Inst. de Ciencias Ambientais, Quimicas e Farmaceuticas. Dept. de Ciencias Exatas e da Terra
Publication Date:
Jul 01, 2012
Product Type:
Journal Article
Resource Relation:
Journal Name: Quimica Nova; Journal Volume: 35; Journal Issue: 7
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; ALKALOIDS; BENZOQUINONES; CARBON 13; DMSO; ENZYME INHIBITORS; FLUORESCENCE; HERBICIDES; HYDROGEN 1; LEAVES; MOLYBDATES; NMR SPECTRA; PHENOL; PHOTOSYNTHESIS; SPINACH; UREA
OSTI ID:
22012567
Country of Origin:
Brazil
Language:
Portuguese
Other Identifying Numbers:
Journal ID: ISSN 0100-4042; TRN: BR12V2870099669
Availability:
Available from http://www.scielo.br/pdf/qn/v35n7/v35n7a20.pdf
Submitting Site:
BRN
Size:
page(s) 1395-1400
Announcement Date:
Jan 10, 2013

Citation Formats

Burger, Marcela Carmen de M., Oliveira, Gracielle S. de, Menezes, Antonio Carlos S, Vieira, Paulo Cezar, Silva, Maria Fatima das G.F. da, and Veiga, Thiago A.M., E-mail: tveiga@unifesp.br. Myrsinoic A acid and its derivative: in vitro inhibitors of photosynthesis; Acido myrsinoico A e derivado: inibidores da fotossintese in vitro. Brazil: N. p., 2012. Web. doi:10.1590/S0100-40422012000700020.
Burger, Marcela Carmen de M., Oliveira, Gracielle S. de, Menezes, Antonio Carlos S, Vieira, Paulo Cezar, Silva, Maria Fatima das G.F. da, & Veiga, Thiago A.M., E-mail: tveiga@unifesp.br. Myrsinoic A acid and its derivative: in vitro inhibitors of photosynthesis; Acido myrsinoico A e derivado: inibidores da fotossintese in vitro. Brazil. https://doi.org/10.1590/S0100-40422012000700020
Burger, Marcela Carmen de M., Oliveira, Gracielle S. de, Menezes, Antonio Carlos S, Vieira, Paulo Cezar, Silva, Maria Fatima das G.F. da, and Veiga, Thiago A.M., E-mail: tveiga@unifesp.br. 2012. "Myrsinoic A acid and its derivative: in vitro inhibitors of photosynthesis; Acido myrsinoico A e derivado: inibidores da fotossintese in vitro." Brazil. https://doi.org/10.1590/S0100-40422012000700020.
@misc{etde_22012567,
title = {Myrsinoic A acid and its derivative: in vitro inhibitors of photosynthesis; Acido myrsinoico A e derivado: inibidores da fotossintese in vitro}
author = {Burger, Marcela Carmen de M., Oliveira, Gracielle S. de, Menezes, Antonio Carlos S, Vieira, Paulo Cezar, Silva, Maria Fatima das G.F. da, and Veiga, Thiago A.M., E-mail: tveiga@unifesp.br}
abstractNote = {Myrsinoic A acid, isolated from Myrsine cuneifolia and its hydrogenated derivative had their effect on photosynthesis tested. The compounds inhibited the electron flow (basal, phosphorylating and uncoupled) from water to methyl viologen; therefore, they act as Hill reaction inhibitors in spinach thylakoids. They inhibited partial reactions of PSII electron flow from water to 2,5-dichloro-1,4-benzoquinone, from water to sodium silicomolybdate, and partially electron flow from diphenylcarbazide to 2,6-dichloroindophenol. Their inhibition sites were at the donor and acceptor sides of PSII, between P{sub 680} and Q{sub A}. Chlorophyll {alpha} fluorescence measurements confirmed the behavior of the compounds (pool of quinones). (author)}
doi = {10.1590/S0100-40422012000700020}
journal = []
issue = {7}
volume = {35}
journal type = {AC}
place = {Brazil}
year = {2012}
month = {Jul}
}