scholarly journals Studies Related to Naturally Occurring Acetylene Compounds. IX. The Occurrence of Methyl dec-8-cis-en4:6-diynoate (= alpha,beta-Dihydro-Matricaria Ester) and 2-cis; 8-trans-Matricaria Ester in Nature.

1952 ◽  
Vol 6 ◽  
pp. 883-892 ◽  
Author(s):  
Kjellrun Stavholt Baalsrud ◽  
Dagny Holme ◽  
Magne Nestvold ◽  
Josef Plíva ◽  
Jörgine Stene Sörensen ◽  
...  
1952 ◽  
Vol 6 ◽  
pp. 893-900 ◽  
Author(s):  
Per Koch Christensen ◽  
Nils Andreas Sörensen ◽  
Bengt Månsson ◽  
W. E. Harvey ◽  
Sven Östling

1954 ◽  
Vol 8 ◽  
pp. 1757-1762 ◽  
Author(s):  
Torger Bruun ◽  
Lars Skatteböl ◽  
Nils Andreas Sörensen ◽  
Nils Andreas Sörensen

1981 ◽  
Vol 193 (2) ◽  
pp. 541-552 ◽  
Author(s):  
L C Packman ◽  
W V Shaw

1. Hybrids of the tetrameric enzyme chloramphenicol acetyltransferase (EC 2.3.1.28) were formed in vivo in a strain of Escherichia coli which harbours two different plasmids, each of which normally confers chloramphenicol resistance and specifies an easily distinguished enzyme variant (type I or type III) which is composed of identical subunits. Cell-free extracts of the dual-plasmid strain were found to contain five species of active enzyme, two of which were the homomeric enzymes corresponding to the naturally occurring tetramers of the type-I (beta 4) and type-III (alpha 4) enzymes. The other three variants were judged to be the heteromeric hybrid variants (alpha 3 beta, alpha 2 beta 2, alpha beta 3). 2. The alpha 3 beta and alpha 2 beta 2 hybrids of chloramphenicol acetyltransferase were purified to homogeneity by combining the techniques of affinity and ion-exchange chromatography. The alpha beta 3 variant was not recovered and may be unstable in vitro. 3. The unique lysine residues that could not be modified with methyl acetimidate in each of the native homomeric enzymes were also investigated in the heteromeric tetramers. 4. Lysine-136 remains buried in each beta subunit of the parental (type I) enzyme and in each of the hybrid tetramers. Lysine-38 of each alpha subunit is similarly unreactive in the native type-III chloramphenicol acetyltransferase (alpha 4), but in the alpha 2 beta 2 hybird lysine-38 of each alpha subunit is fully exposed to solvent. Another lysine residue, fully reactive in the alpha 4 enzyme, was observed to be inaccessible to modification in the symmetrical hybrid. The results obtained for the alpha 3 beta enzyme suggest that lysine-38 in two subunits and a different lysine group (that identified in the alpha 2 beta 2 enzyme) in the third alpha subunit are buried. 5. A tentative model for the subunit interactions of chloramphenicol acetyltransferase is proposed on the basis of the results described.


1969 ◽  
Vol 22 (4) ◽  
pp. 751 ◽  
Author(s):  
JS Sorensen ◽  
NA Sorensen

Two Australian members of the genus Erigeron L. (Compositae, tribe Astereae) have been investigated with particular regard to their content of acetylenic compounds. E. conyzoides F. Muell. contained the methyl esters (I) and (II) of acetylenic carboxylic acids and their corresponding lactones (III) and (IV) and in this resemble the numerous Erigeron spp. of the northern hemisphere investigated earlier. Of the collective species E. pappochroma Labill. three Tasmanian and two Snowy Mountain collections were investigated. None of them contained the acetylenic compounds characteristic of typical Erigeron. Three of these collections contained some simple acetylenic alcohols, (V)-(IX); some of these are characteristic compounds of other genera of the tribus Astereae. In two collections acetylenic compounds were seemingly absent; but dill apiol (XI) was found in appreciable amounts.


1953 ◽  
Vol 7 ◽  
pp. 1375-1387 ◽  
Author(s):  
Gjertrud Moen Tronvold ◽  
Magne Nestvold ◽  
Dagny Holme ◽  
Jörgine Stene Sörensen ◽  
Nils Andreas Sörensen

1966 ◽  
Vol 20 ◽  
pp. 992-1002 ◽  
Author(s):  
Jørgine Stene Sørensen ◽  
Nils Andreas Sørensen ◽  
Bodil Jerslev ◽  
E. Kulonen ◽  
J. Brunvoll ◽  
...  

1954 ◽  
Vol 8 ◽  
pp. 1763-1768 ◽  
Author(s):  
Jörgine Stene Sörensen ◽  
Nils Andreas Sörensen ◽  
Eldbjörg Tuxen Borlaug ◽  
Nils Andreas Sörensen

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