Imazaquin and chlorsulfuron resistance and cross resistance in mutants of Chlamydomonas reinhardtii

1988 ◽  
Vol 213 (2-3) ◽  
pp. 394-399 ◽  
Author(s):  
Tom Winder ◽  
Martin H. Spalding
1993 ◽  
Vol 48 (3-4) ◽  
pp. 146-151 ◽  
Author(s):  
Walter Oettmeier ◽  
Klaus Masson ◽  
Ralf Kloos ◽  
Ellen Reil

Abstract The orientation of acridones, xanthones, 1,4-benzo-and naphthoquinones within the photosystem II QB herbicide-binding niche was studied by means of mild trypsination and by estimation of pI50-values in Chlamydomonas reinhardtii D 1 mutants (Val219 > lie, Ala251 > Val, Phe255 > Tyr, Ser264 > Ala, Asn266 > Thr, and Leu275 > Phe). As judged from the R/S-values (ratios of I50 -values resistant versus susceptible type) close to 1 in all mutants, the acridones and xanthones do not have strong interactions with the parent amino acids. Contrary, the quinones exhibit extreme low R/S-values down to 0.003 (for 2,5-dibromo-3-methyl-6-isopropyl-1,4-benzoquinone; DBMIB) in the Ser264 mutant. This extreme negative cross resistance or supersensitivity indicates that the quinones do not form a hydrogen bond to the serine hydroxyl group.


1993 ◽  
Vol 71 (1) ◽  
pp. 174-182 ◽  
Author(s):  
Douglas F. Bray ◽  
John R. Bagu ◽  
Kazuo Nakamura

A mutant (NL-51) of the unicellular green alga Chlamydomonas reinhardtii Dangeard isolated from a wild-type strain (137c+) was shown to be resistant to the bipyridilium herbicide paraquat at the concentration at which growth of the wild type was inhibited. Tetrad analysis from a cross between the mutant and the wild type showed 2:2 segregation, indicating that the resistance is under control of a single gene. Cross-resistance of the mutant to methionine and to methionine combined with riboflavin suggested that the resistance is due to increased levels of one of the enzymes capable of detoxifying active oxygens. Ultrastructural examination of mutant and wild-type cells exposed to paraquat revealed that the mutant cells were 3 to 4 times more resistant, but both strains showed the same sequence of deterioration. Damage was first manifested as swelling of the mitochondria and dilation of the perinuclear space. This was followed by disintegration of the nuclear matrix and the chloroplast thylakoids. Key words: Chlamydomonas reinhardtii, methionine resistance, paraquat, paraquat-resistant mutant, ultrastructure.


Genetics ◽  
1989 ◽  
Vol 123 (2) ◽  
pp. 281-292 ◽  
Author(s):  
E H Harris ◽  
B D Burkhart ◽  
N W Gillham ◽  
J E Boynton

Abstract Mutants resistant to streptomycin, spectinomycin, neamine/kanamycin and erythromycin define eight genetic loci in a linear linkage group corresponding to about 21 kb of the circular chloroplast genome of Chlamydomonas reinhardtii. With one exception, all of these mutants represent single base-pair changes in conserved regions of the genes encoding the 16S and 23S chloroplast ribosomal RNAs. Streptomycin resistance can result from changes at the bases equivalent to Escherichia coli 13, 523, and 912-915 in the 16S gene, or from mutations in the rps12 gene encoding chloroplast ribosomal protein S12. In the 912-915 region of the 16S gene, three mutations were identified that resulted in different levels of streptomycin resistance in vitro. Although the three regions of the 16S rRNA mutable to streptomycin resistance are widely separated in the primary sequence, studies by other laboratories of RNA secondary structure and protein cross-linking suggest that all three regions are involved in a common ribosomal neighborhood that interacts with ribosomal proteins S4, S5 and S12. Three different changes within a conserved region of the 16S gene, equivalent to E. coli bases 1191-1193, confer varying levels of spectinomycin resistance, while resistance to neamine and kanamycin results from mutations in the 16S gene at bases equivalent to E. coli 1408 and 1409. Five mutations in two genetically distinct erythromycin resistance loci map in the 23S rDNA of C. reinhardtii, at positions equivalent to E. coli 2057-2058 and 2611, corresponding to the rib3 and rib2 loci of yeast mitochondria respectively. Although all five mutants are highly resistant to erythromycin, they differ in levels of cross-resistance to lincomycin and clindamycin. The order and spacing of all these mutations in the physical map are entirely consistent with our genetic map of the same loci and thereby validate the zygote clone method of analysis used to generate this map. These results are discussed in comparison with other published maps of chloroplast genes based on analysis by different methods using many of the same mutants.


Planta Medica ◽  
2015 ◽  
Vol 81 (11) ◽  
Author(s):  
M Choules ◽  
Y Yu ◽  
SH Cho ◽  
J Anderson ◽  
W Gao ◽  
...  
Keyword(s):  

ENTOMON ◽  
2019 ◽  
Vol 44 (2) ◽  
pp. 127-132
Author(s):  
M. Visnupriya ◽  
N. Muthukrishnan

Field population of Spodoptera litura from tomato ( resistant to the majority of the conventional insecticide molecules) were subjected to the in vivo toxicity of spinetoram 12 SC to assess whether cross resistance exists or not. Untreated larvae of both field and laboratory strains showed no mortality during 48 hours of feeding. After 48 hours of feeding on spinetoram 12 SC treated leaves, LC50s of field larvae were 0.28, 0.93, 3.71 and 7.11 ppm for the 2nd, 3rd, 4th and 5th instars of S. litura respectively. However, in the laboratory strain these values were 1.12, 5.86, 36.72 and 91.55 ppm for 2nd, 3rd, 4th and 5th instars of S. litura respectively. Resistance ratio was 0.25, 0.16, 0.10 and 0.08 for the 2nd instar up to the 5th instar of S. litura.


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