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Distribution and Characteristics of Triazine-Resistant Powell Amaranth (Amaranthus powellii) in Idaho

Published online by Cambridge University Press:  12 June 2017

Charlotte V. Eberlein ,
Kassim Al-Khatib ,
Mary J. Guttieri  and
E. Patrick Fuerst
Charlotte V. Eberlein
Affiliation:
Univ. Idaho, Aberdeen, ID 83210
Kassim Al-Khatib
Affiliation:
Washington State Univ., Prosser, WA 99350
Mary J. Guttieri
Affiliation:
Univ. Idaho, Aberdeen, ID 83210
E. Patrick Fuerst
Affiliation:
Washington State Univ., Pullman, WA 99164
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Abstract

A triazine-resistant (TR) biotype of Powell amaranth was discovered in 1989 in a potato field treated with metribuzin. A survey of all agricultural counties in Idaho showed that the TR Powell amaranth infestation was localized in the southeastern corner of Gooding county in southern Idaho. To determine the mechanism of triazine resistance, I50 values for inhibition of photosystem II were determined for atrazine, metribuzin, and diuron using thylakoids isolated from TR and triazine-susceptible (TS) biotypes. TR/TS ratios based on I50 values were 134 for atrazine, 62 for metribuzin, and 1.9 for diuron. Results of binding studies with atrazine and metribuzin were consistent with the I50 studies, indicating that resistance was due to reduced binding of triazines to the thylakoid membrane D1 protein. Sequencing the chloroplast psbA gene from TR and TS biotypes revealed a serine 264 to glycine change in the TR biotype. The mutation presumably resulted in reduced hydrogen bonding between triazine herbicides and the Dl protein.

Keywords

Atrazine, 6-chloro-N-ethyl-N′-(1-methylethyl)-1,3,5-triazine-2,4-diaminediuron, N′-(3,4-dichlorophenyl)-N, N-dimethylureametribuzin, 4-amino-6-(1,1-dimethylethyl)-3-(methylthio)-1,2,4-triazin-5(4H)-onePowell amaranth, Amaranthus powellii S. Wats. #3 AMAPOpotato, Solanum tuberosum L.Herbicide resistanceDNA sequencechloroplast assayherbicide bindingAMAPO

Information

Type
Physiology, Chemistry, and Biochemistry
Information
Weed Science , Volume 40 , Issue 4 , December 1992 , pp. 507 - 512
Copyright
Copyright © 1992 by the Weed Science Society of America 

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References

Literature Cited

1. Ahrens, W. H., Wax, L. M., and Stoller, E. W. 1981. Identification of triazine-resistant Amaranthus spp. Weed Sci. 29:345–348.Google Scholar
2. Al-Khatib, K. and Paulsen, G. M. 1989. Enhancement of thermal injury to photosynthesis in wheat plants and thylakoids by high light intensity. Plant Physiol. 90:1041–1048.Google Scholar
3. Andersen, R. N. 1988. Outcrossing in velvetleaf (Abutilon theophrasti). Weed Sci. 36:599–602.Google Scholar
4. Andersen, R. N. and Gronwald, J. W. 1987. Noncytoplasmic inheritance of atrazine tolerance in velvetleaf (Abutilon theophrasti). Weed Sci. 35:496–498.Google Scholar
5. Arnon, D. I. 1949. Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris . Plant Physiol. 24:1–15.Google Scholar
6. Doyle, J. J. and Doyle, J. L. 1990. Isolation of plant DNA from fresh tissue. Focus 12:13–15.Google Scholar
7. Eberlein, C. V., Al-Khatib, K., Guttieri, M. J., and Fuerst, E. P. 1991. Distribution, characteristics, and control of triazine resistant Powell amaranth in Idaho. Proc. West. Soc. Weed Sci. 44:112–113.Google Scholar
8. Erickson, J. M., Rahire, M., Bennoun, P., Delepelaire, P., Diner, B., and Rochaiz, J. D. 1984. Herbicide resistance in Chlamydomonas reinhardtii results from a mutation in the chloroplast gene for the 32-kilodalton protein of photosystem II. Proc. Nat. Acad. Sci. U.S.A. 81 3617–3621.Google Scholar
9. Fuerst, E. P., Arntzen, C. J., Pfister, K., and Penner, D. 1986. Herbicide cross-resistance in triazine-resistant biotypes of four species. Weed Sci. 34:344–353.CrossRefGoogle Scholar
10. Fuerst, E. P. and Norman, M. A. 1991. Interactions of herbicides with photosynthetic electron transport. Weed Sci. 39:458–464.Google Scholar
11. Gronwald, J. W., Andersen, R. N., and Yee, C. 1989. Atrazine resistance in velvetleaf (Abutilon theophrasti) due to enhanced atrazine detoxification. Pestic. Biochem. Physiol. 34:149–163.Google Scholar
12. Hirschberg, J. and McIntosh, L. 1983. Molecular basis of herbicide resistance in Amaranthus hybridus . Science 222:1346–1348.Google Scholar
13. Holt, J. S. and LeBaron, H. M. 1990. Significance and distribution of herbicide resistance. Weed Technol. 4:141–149.Google Scholar
14. Naber, D., Johanningmeier, U., and van Rensen, J.J.S. 1990. A rapid method for partial mRNA and DNA sequence analysis of the photosystem II psbA gene. Z. Naturforsch. 45c:418–422.Google Scholar
15. Souza-Machado, V. and Bandeen, J. D. 1982. Genetic analysis of chloroplast atrazine resistance in Brassica campestris—cytoplasmic inheritance. Weed Sci. 30:281–285.Google Scholar
16. Vencill, W. K. and Foy, C. L. 1988. Distribution of triazine-resistant smooth pigweed (Amaranthus hybridus) and common lambsquarters (Chenopodium album) in Virginia. Weed Sci. 36:497–499.CrossRefGoogle Scholar