scholarly journals The Conversion of Parkeol into its 24,25-Epoxide by Tissue Cultures of Nicotiana tabacum

1970 ◽  
Vol 14 (2) ◽  
pp. 284-288 ◽  
Author(s):  
Phillip C. Schaefer ◽  
Francois Reinach ◽  
Guy Ourisson
1973 ◽  
Vol 51 (1) ◽  
pp. 151-156 ◽  
Author(s):  
P. S. Baur ◽  
C. H. Walkinshaw ◽  
R. S. Halliwell ◽  
V. E. Scholes

Suspension and stationary habituated tobacco tissue cultures were examined histologically and cytologically after treatment with 0.22 g of lunar material. The treated and untreated tissues differed in chloroplast structure and distribution, degree of cell association, cytoplasmic vacuolation and vesiculation, and living to nonliving ratios.


Plant Science ◽  
1986 ◽  
Vol 45 (2) ◽  
pp. 125-132 ◽  
Author(s):  
Gilberto Barbante Kerbauy ◽  
JoséAntonio Peters ◽  
Kurt Gunther Hell

1960 ◽  
Vol 43 (4) ◽  
pp. 841-851 ◽  
Author(s):  
Ludwig Bergmann

The cultivation of single cells of Nicotiana tabacum L. var. "Samsun" and Phaseolus vulgaris L. var. "Early Golden Cluster" on a thin agar layer in Petri dishes is described. Under these conditions about 20 per cent of the cells divided repeatedly and established tissue clones which could be isolated and maintained as growing tissue cultures. It was possible also to follow the successive divisions of isolated cells and to observe their behavior during cytogenesis under the microscope.


1972 ◽  
Vol 27 (10) ◽  
pp. 1205-1215 ◽  
Author(s):  
Wolfgang Beisenherz

The RNA metabolism in tissue cultures of Nicotiana tabacum has been studied by incorporation of radioactive phosphate. The RNA was extracted by phenol-kresol-hydroxychinon and fractionated by MAK columns. A rapidly labelled RNA fraction was eluted from the MAK column after the rRNA components. Its base ratio differed from the latter in that the AMP content (28,6%) was higher than the GMP content (26,0%). Sedimentation analysis on sucrose gradients showed a sedimentation coefficient of 37 -38s. The life time of the 37-38s RNA fraction in chase experiments was 3,5-4 hours. Differential centrifugation of tissue homogenates revealed that the labelled 37-38s RNA was associated with particles sedimented by low speed centrifugation. No 37-38s RNA could be detected in the ribosomal fraction and the supernatant. During chase experiments label appeared in the rRNA components. It could be excluded by thin layer chromatographic separation of 32P labelled compounds that this label originated from 32P-o-phosphate or labelled organic phosphates except of the rapidly labelled 37-38s RNA. From this it was concluded that the 37-38s RNA is a precursor of the rRNA.


Weed Science ◽  
1978 ◽  
Vol 26 (6) ◽  
pp. 527-530 ◽  
Author(s):  
J. B. Huffman ◽  
N. D. Camper

Tobacco(Nicotiana tabacumL. ‘X-73’) callus tissue cultures were used in a bioassay system for determining the effect of the following substituted 2,6-dinitroaniline herbicides on growth: trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine); oryzalin (3,5-dinitro-N4,N4-dipropylsulfanilamide); benefin(N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-toluidine); AC 92390(N-sec-butyl-2,6-dinitro-3,4-xylidine); penoxalin [N-(1-ethylpropyl)-2,6-dinitro-3,4-xylidine]; GS-38946(N-ethyl-N-tetrahydrofurfuryl-4-trifluoromethyl-2,6-dinitroaniline); chlornidine [N,N-di(2-chloroethyl)-4-methyl-2,6-dinitroaniline]; nitralin [4-(methylsulfonyl)2,6-dinitro-N,N-dipropylaniline]; dinitramine(N4,N4-diethyl-α,α,α-trifluoro-3,5-dinitrotoluene-2,4-diamine); isopropalin (2,6-dinitro-N,N-dipropylcumidine), and profluralin [N(cyclopropylmethyl)-α,α,α-trifluoro-2,6-dinitro-N-propyl-p-toluidine]. The molar concentration required to inhibit fresh weight gain by 50% (I50) was determined by using linear regression analysis on data from a range of five concentrations of each chemical. I50values did not correlate with structural variations or available physical constants. Herbicides listed in order of increasing activity are AC 92390< GD-38946<profluralin = isopropalin<benefin = chlornidine = trifluralin = nitralin<oryzalin = penoxalin < dinitramine. Exogenously applied D-α-tocopherol acetate at 100 times the I50concentrations decreased the inhibition of tissue growth by the herbicides.


1965 ◽  
Vol 20 (12) ◽  
pp. 1297-1301 ◽  
Author(s):  
L. Bergmann ◽  
W. Thies ◽  
K. Erdelsky

Tissue cultures of Nicotiana tabacum var. “Samsun” contain an array of phenolic compounds. Beside the known glucose and quinyl esters of the hydroxycinnamic acids three hitherto unreported phenolic acid esters were isolated from tobacco tissue cultures. The analytical and spectral data presented in this paper lead to the conclusion that these compounds are glucosamine esters of p-coumaric, caffeic, and ferulic acid.


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