Biochemistry and Genetic Control of the Photosystem II Herbicide Target Site

2020 ◽  
pp. 1-24
Author(s):  
L. Mets ◽  
A. Thiel
Weed Science ◽  
1991 ◽  
Vol 39 (3) ◽  
pp. 317-323 ◽  
Author(s):  
Michael W. M. Burnet ◽  
Orville B. Hildebrand ◽  
Joseph A. M. Holtum ◽  
Stephen B. Powles

A biotype of rigid ryegrass (Lolium rigidum G. ♯ LOLRI) has become resistant to amitrole and atrazine after 10 yr of exposure to a mixture of these herbicides. Resistance has also been demonstrated to the chloro-s-triazines: simazine, cyanazine, propazine; the methylthios-triazines: ametryn, prometryn; the substituted ureas: chlortoluron, isoproturon, metoxuron, diuron, fluometuron, methazole; and the triazinone herbicide metribuzin. The biotype remains susceptible to chlorsulfuron, metsulfuron, sulfometuron, sethoxydim, diclofop, fluazifop, glyphosate, carbetamide, and oxyfluorfen. Inhibition of oxygen evolution by atrazine, diuron, and metribuzin was similar in thylakoids isolated from both resistant and susceptible biotypes. Therefore, resistance to the photosystem II inhibitors is not caused by an alteration of the target site of these herbicides. Resistant plants treated with a 3-h pulse of 0.12 mM chlortoluron recover photosynthetic activity more rapidly than susceptible plants. This suggests that the basis for resistance is enhanced metabolism or sequestration of the herbicide within the leaf.


Weed Science ◽  
2021 ◽  
pp. 1-34
Author(s):  
David B. Westerveld ◽  
Nader Soltani ◽  
David C. Hooker ◽  
Darren E. Robinson ◽  
Patrick J. Tranel ◽  
...  

Abstract Photosystem II (PS II)-inhibitor herbicide resistance in Ontario waterhemp [Amaranthus tuberculatus (Moq.) Sauer] population is conferred via target-site resistance (TSR) and non-target-site resistance (NTSR) mechanisms. Metribuzin-resistant (MR) A. tuberculatus is due to TSR,. Conversely, in other populations of PS II-resistant A. tuberculatus, plants are resistant to atrazine but metribuzin-sensitive (MS). The objective of this study was to determine the biologically-effective-dose of metribuzin applied PRE and POST for the control of MS and MR A. tuberculatus. Ten field experiments were conducted in 2019 and 2020 to determine the effective doses of metribuzin for 50, 80, and 95% control of MS and MR A. tuberculatus. Metribuzin applied PRE at the calculated doses of 133, 350, and 1070 g ai ha-1 controlled MS A. tuberculatus 50, 80, and 95%, respectively, whereas the calculated doses of 7868 and 17533 g ai ha-1 controlled MR A. tuberculatus 50 and 80%, respectively at 12 WAA. Metribuzin applied POST at the calculated doses of 245 and 1480 g ai ha-1 controlled MS A. tuberculatus 50 and 80%, respectively; the calculated dose for 50% MR A. tuberculatus control was greater than the highest dose (17920 g ai ha-1) included in this study. Metribuzin at 560 and 1120 g ha-1 and pyroxasulfone/flumioxazin (240 g ai ha-1) applied PRE controlled MS A. tuberculatus 88, 95, and 98%, respectively at 12 WAA. The aforementioned treatments controlled MR A. tuberculatus 0, 4, and 93%, respectively at 12 WAA. Metribuzin at 560 and 1120 g ha-1 and fomesafen (240 g ai ha-1) applied POST controlled MS A. tuberculatus 65, 70, and 78%, and MR A. tuberculatus 0, 1, and 49%, respectively at 12 WAA. Based on these results, NTSR PS II-resistant A. tuberculatus (enhanced metabolism) is controlled with metribuzin applied PRE and POST, in contrast TSR PS II-resistant A. tuberculatus (glycine264serine altered target site) is not controlled with metribuzin.


Author(s):  
Kathleen M. Marr ◽  
Mary K. Lyon

Photosystem II (PSII) is different from all other reaction centers in that it splits water to evolve oxygen and hydrogen ions. This unique ability to evolve oxygen is partly due to three oxygen evolving polypeptides (OEPs) associated with the PSII complex. Freeze etching on grana derived insideout membranes revealed that the OEPs contribute to the observed tetrameric nature of the PSIl particle; when the OEPs are removed, a distinct dimer emerges. Thus, the surface of the PSII complex changes dramatically upon removal of these polypeptides. The atomic force microscope (AFM) is ideal for examining surface topography. The instrument provides a topographical view of individual PSII complexes, giving relatively high resolution three-dimensional information without image averaging techniques. In addition, the use of a fluid cell allows a biologically active sample to be maintained under fully hydrated and physiologically buffered conditions. The OEPs associated with PSII may be sequentially removed, thereby changing the surface of the complex by one polypeptide at a time.


1994 ◽  
Vol 92 (1) ◽  
pp. 181-187
Author(s):  
Maria T. Giardi ◽  
Josef Komenda ◽  
Jiri Masojidek

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