Uptake of methylamine via an inducible, energy-dependent transport system in the facultative methylotroph Arthrobacter P1

1982 ◽  
Vol 133 (4) ◽  
pp. 261-266 ◽  
Author(s):  
Lubbert Dijkhuizen ◽  
Lex de Boer ◽  
Roelof H. Boers ◽  
Wim Harder ◽  
Wil N. Konings
1980 ◽  
Vol 58 (10) ◽  
pp. 797-803 ◽  
Author(s):  
D. M. Ashton ◽  
G. D. Sweet ◽  
J. M. Somers ◽  
W. W. Kay

The citrate analogue, 2-fluoro-L-erythro-[3,4,5,6-14C]citrate was synthesized as a probe for the citrate transport system of Salmonella typhimurium. This analogue was actively transported by an inducible energy-dependent transport system with high affinity for fluorocitrate (Km = 3.3 μM), and this transport system was inhibited competitively by citrate and isocitrate. Fluorocitrate was shown to be a competitive inhibitor of the citrate-binding protein (C protein) of this organism (Ki = 4–5 μM). Analogue resistant mutants were simultaneously defective in fluorocitrate transport as well as the C protein and the affected allele, tctC, was located at 59 units on the S. typhimurium chromosome map. These tctC mutants were shown to be specifically defective in K+-dependent fluorocitrate transport but still retained another system capable of transporting fluorocitrate in the presence of both Na+ and K+.


1966 ◽  
Vol 50 (1) ◽  
pp. 9-24 ◽  
Author(s):  
J. Gordin Kaplan ◽  
Wanda Tacreiter

There are two distinct components of the system which limits the rate at which intact cells of S. cerevisiae C hydrolyze external ß-glucosides; one component requires metabolic energy and the other is stereospecific for ß-glucosides. The stereospecific component is localized at the cell membrane, as shown by its sensitivity to heavy metal inhibitors which did not penetrate the cell under the conditions used. It was shown that cellobiose-grown cells were able to remove cellobiose from the medium in which they were incubated, and that the cellobiose uptake system was identical to that which limits the patent ß-glucosidase activity. In order to test the hypothesis that the system in question was a transport system, for ß-glucosides the ability of cellobiose-grown cells to take up 14C-labeled methyl-ß-glucoside (MBG) was studied. The induced cells were able to take up MBG-14C and the label could be partially chased out by cold MBG and cellobiose; glucose-grown cells could not incorporate label. However, induced cells could not take up label when incubated with 14C-MBG, thus excluding the hypothesis of transport of intact ß-glucosides. It was concluded that the stereospecific membrane component was actually a ß-glucosidase, coupled to an energy-dependent transport system for the glucose moiety; the function of the latter was rate-limiting in the over-all activity of the entire system.


1989 ◽  
Vol 63 (1-2) ◽  
pp. 53-60
Author(s):  
W. Saurin ◽  
E. Francoz ◽  
P. Martineau ◽  
A. Charbit ◽  
E. Dassa ◽  
...  

1985 ◽  
Vol 5 (11) ◽  
pp. 1269-1279 ◽  
Author(s):  
Hamid M. Said ◽  
Daniel Hollander ◽  
Yen Duong

2006 ◽  
Vol 18 (19) ◽  
pp. 4581-4587 ◽  
Author(s):  
B Lassagne ◽  
B Raquet ◽  
J M Broto ◽  
J González

Extremophiles ◽  
2020 ◽  
Author(s):  
Lei Zhai ◽  
Jiuyan Xie ◽  
Huijun Feng ◽  
Sijia Sun ◽  
Kun Cheng ◽  
...  

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