metabolic transport
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Planta ◽  
2018 ◽  
Vol 249 (2) ◽  
pp. 377-391 ◽  
Author(s):  
Claudia Birkemeyer ◽  
Natalia Osmolovskaya ◽  
Ludmila Kuchaeva ◽  
Elena Tarakhovskaya

Microbiology ◽  
2017 ◽  
Vol 163 (11) ◽  
pp. 1720-1734 ◽  
Author(s):  
Susanne Bauer ◽  
Jonas Helmreich ◽  
Marie Zachary ◽  
Marc Kaethner ◽  
Elisabeth Heinrichs ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e100963 ◽  
Author(s):  
Xiao Cui ◽  
Lars Geffers ◽  
Gregor Eichele ◽  
Jun Yan

2010 ◽  
Vol 192 (22) ◽  
pp. 5962-5971 ◽  
Author(s):  
Ryan C. Hunter ◽  
Dianne K. Newman

ABSTRACT Pyomelanin overproduction is a common phenotype among Pseudomonas aeruginosa isolates recovered from cystic fibrosis and urinary tract infections. Its prevalence suggests that it contributes to the persistence of the producing microbial community, yet little is known about the mechanisms of its production. Using transposon mutagenesis, we identified factors that contribute to melanogenesis in a clinical isolate of P. aeruginosa. In addition to two enzymes already known to be involved in its biosynthesis (homogentisate dioxygenase and hydroxyphenylpyruvate dioxygenase), we identified 26 genes that encode regulatory, metabolic, transport, and hypothetical proteins that contribute to the production of homogentisic acid (HGA), the monomeric precursor of pyomelanin. One of these, PA14_57880, was independently identified four times and is predicted to encode the ATP-binding cassette of an ABC transporter homologous to proteins in Pseudomonas putida responsible for the extrusion of organic solvents from the cytosol. Quantification of HGA production by P. aeruginosa PA14 strains missing the predicted subcomponents of this transporter confirmed its role in HGA production: mutants unable to produce the ATP-binding cassette (PA14_57880) or the permease (PA14_57870) produced substantially less extracellular HGA after growth for 20 h than the parental strain. In these mutants, concurrent accumulation of intracellular HGA was observed. In addition, quantitative real-time PCR revealed that intracellular accumulation of HGA elicits upregulation of these transport genes. Based on their involvement in h omogentisic a cid t ransport, we rename the genes of this operon hatABCDE.


2008 ◽  
Vol 58 (3) ◽  
pp. 313-319
Author(s):  
Lonneke Eeuwes ◽  
Robert Peters ◽  
Franklin Bretschneider

AbstractAdministration of the cell impermeant fluorescent K+ and Na+ probes potassium-binding fluorescent indicator (PBFI) and sodium-binding fluorescent indicator (SBFI) to the lumina of ampullary electroreceptor organs in the transparent catfish Kryptopterus bicirrhis (Valenciennes 1840), demonstrated an unexpected high concentration of K+ ions: 50 mM. Since the lumina of the ampullary organs are in open contact with the surrounding water, such a high K+ concentration inside the lumen can be maintained only by heavy metabolic transport. The implications of this finding for stimulus transduction in freshwater ampullary electroreceptor cells are discussed.


BMC Genomics ◽  
2008 ◽  
Vol 9 (1) ◽  
pp. 490 ◽  
Author(s):  
Olga Martínez-Augustin ◽  
Manel Merlos ◽  
Antonio Zarzuelo ◽  
María Suárez ◽  
Fermín de Medina

2004 ◽  
Vol 287 (6) ◽  
pp. G1150-G1157 ◽  
Author(s):  
Aliye Uc ◽  
John B. Stokes ◽  
Bradley E. Britigan

Heme prosthetic groups are vital for all living organisms, but they can also promote cellular injury by generating reactive oxygen species. Therefore, intestinal heme absorption and distribution should be carefully regulated. Although a human intestine brush-border heme receptor/transporter has been suggested, the mechanism by which heme crosses the apical membrane is unknown. After it enters the cell, heme is degraded by heme oxygenase-1 (HO-1), and iron is released. We hypothesized that heme transport is actively regulated in Caco-2 cells. Cells exposed to hemin from the basolateral side demonstrated a higher HO-1 induction than cells exposed to hemin from the apical surface. Hemin secretion was more rapid than absorption, and net secretion occurred against a concentration gradient. Treatment of the apical membrane with trypsin increased hemin absorption by threefold, but basolateral treatment with trypsin had no effect on hemin secretion. Neither apical nor basolateral trypsin changed the paracellular pathway. We conclude that heme is acquired and transported in both absorptive and secretory directions in polarized Caco-2 cells. Secretion is via an active metabolic/transport process. Trypsin applied to the apical surface increased hemin absorption, suggesting that protease activity can uncover a process for heme uptake that is otherwise quiescent. These processes may be involved in preventing iron overload in humans.


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