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Cyclo(Phe-Pro) produced by Vibrio species passes through biological membranes by simple diffusion

Title
Cyclo(Phe-Pro) produced by Vibrio species passes through biological membranes by simple diffusion
Authors
Park N.-Y.Cho Y.B.Kim O.B.Kim K.-S.
Ewha Authors
김옥빈
SCOPUS Author ID
김옥빈scopus
Issue Date
2020
Journal Title
Applied Microbiology and Biotechnology
ISSN
0175-7598JCR Link
Citation
Applied Microbiology and Biotechnology vol. 104, no. 15, pp. 6791 - 6798
Keywords
Cyclic dipeptideCyclo(Phe-Pro)Simple diffusionVibrio vulnificus
Publisher
Springer
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Abstract: Cyclo(Phe-Pro) (cFP), produced by the Vibrio species, plays the dual roles of being a signaling molecule and a virulence factor. Acting modes of this compound have recently been characterized at the molecular level. Nevertheless, the method by which this compound passes across biological membranes remains obscure. Using radiolabeled cFP, we examined the kinetics of transport for this compound across membranes using V. vulnificus, Escherichia coli, and sheep red blood cells. We observed that cFP was taken up by these cells in a concentration-dependent manner and was not affected by the addition of the proton ionophore carbonyl cyanide m-chlorophenyl hydrazone (CCCP), suggesting that cFP is taken up by passive transport. The kinetics of uptake of cFP by the above three types of cells revealed no significant differences, indicating that no specific protein is involved in this process. When the intracellular accumulation of cFP in the tested cells was measured, the concentrations did not exhibit significant differences between the 1-min and 10-min time points after cFP was added to the culture. In contrast, the intracellular concentration of fumarate, which is well known to be taken up by cells via active transport, was significantly higher at the 10-min than at the 1-min time point after addition. Taken together, this study shows that cFP is a diffusible molecule that does not require energy for transportation across biological membranes, and that cFP does not need membrane machinery in order to cross membranes and consequently act as a virulence factor or signal. Key Points: • Kinetics of cFP uptake into cells of V. vulnificus, E. coli, or RBS was studied. • The uptake was not saturated and required no energy, indicating passive transport. • The lack of cell specificity in cFP uptake means no specific protein is needed. • Therefore, the cFP moves across the biological membrane by simple diffusion. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.
DOI
10.1007/s00253-020-10646-4
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자연과학대학 > 생명과학전공 > Journal papers
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