Nomenclature Abstract for Pseudomonas acidovorans den Dooren de Jong 1926 (Approved Lists 1980).

2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
Nicole Danielle Osier ◽  
George M Garrity
Keyword(s):  
Pseudomonas Acidovorans

scholarly journals Polyamines of Pseudomonas acidovorans

1973 ◽  
Vol 114 (3) ◽  
pp. 1365-1366 ◽  
Author(s):  
E. Karrer ◽  
R. J. Bose ◽  
R. A. J. Warren
Keyword(s):  
Pseudomonas Acidovorans

Continuous degradation of 3-chloroaniline by calcium-alginate-entrapped cells of Pseudomonas acidovorans CA28: influence of additional substrates

1991 ◽  
Vol 35 (4) ◽  
Author(s):  
Andreas Ferschl ◽  
Michael Loidl ◽  
G�nther Ditzelm�ller ◽  
Christel Hinteregger ◽  
Franz Streichsbier
Keyword(s):  
Calcium Alginate ◽  
Pseudomonas Acidovorans

The pH-dependent uptake of putrescine by Pseudomonas acidovorans and its incorporation into bacteriophage DNA

1983 ◽  
Vol 29 (7) ◽  
pp. 827-829 ◽  
Author(s):  
D. L. Bruce ◽  
R. A. J. Warren
Keyword(s):  
Active Transport ◽  
Transport System ◽  
Normal Condition ◽  
Intracellular Pool ◽  
Pseudomonas Acidovorans ◽  
Ph Dependent ◽  
Active Transport System

Lack of an active transport system prevents Pseudomonas acidovorans taking up putrescine under normal condition of growth. At pH 9.5, however, putrescine does enter the cell. That putrescine enters the intracellular pool is shown by its conversion to 2-hydroxyputrescine and spermidine after the cells are returned to pH 7.0. The accumulated putrescine can be used to label specifically the α-putrescinylthymine residues of bacteriophage [Formula: see text] DNA.

Pyrimidine metabolism in Pseudomonas acidovorans

1974 ◽  
Vol 20 (4) ◽  
pp. 427-433 ◽  
Author(s):  
Rod A. Kelln ◽  
R. A. J. Warren
Keyword(s):  
Biosynthetic Pathway ◽  
Wild Type Strain ◽  
De Novo ◽  
Nucleic Acid Metabolism ◽  
Aspartate Transcarbamylase ◽  
Bacteria Growth ◽  
Deoxycytidine Deaminase ◽  
Lag Period ◽  
Pseudomonas Acidovorans ◽  
Salvage Pathways

Pseudomonas acidovorans lacks a number of enzymes of the salvage pathways of nucleic acid metabolism, including uridine phosphorylase, purine nucleoside phosphorylase, cytidine (deoxycytidine) deaminase and thymidine phosphorylase, and probably uridine kinase and deoxycytidine kinase. Its growth is inhibited by adenosine and deoxyadenosine. The level of aspartate transcarbamylase is the same in extracts of P. acidovorans grown in minimal medium ± 25 μg uracil/ml, and the enzyme appears to be insensitive to nucleotides which affect this enzyme in other bacteria. Growth of two pyrimidine-requiring mutants of P. acidovorans is supported by uracil or cytosine but not by their nucleosides nor by intermediates of the de novo pyrimidine biosynthetic pathway. Concentrations of uracil greater than 50 μg/ml have the unusual effect of lengthening the lag period of the mutants. The wild-type strain is not inhibited by uracil.

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