Active Transport Systems

Calcium is absorbed from the intestine by facilitated diffusion and active transport. In the former, Ca " moves from the mucosal to the serosal compartments along a concentration gradient. The active transport system requires a cation pump. In both processes, a calcium-binding protein (CaBP) is thought to be required for the transport. Synthesis of CaBP is activated by 1,25-DHCC. In the active transport, release of Ca " from the mucosal cell into... 

Biochemically, most quaternary ammonium compounds function as receptor-specific mediators. Because of their hydrophilic nature, small molecule quaternaries caimot penetrate the alkyl region of bdayer membranes and must activate receptors located at the cell surface. Quaternary ammonium compounds also function biochemically as messengers, which are generated at the inner surface of a plasma membrane or in a cytoplasm in response to a signal. They may also be transferred through the membrane by an active transport system. 

All Active Transport Systems Are Energy-Coupling Devices... 

Fructose is present outside a cell at 1 /iM concentration. An active transport system in the plasma membrane transports fructose into this cell, using the free energy of ATP hydrolysis to drive fructose uptake. Assume that one fructose is transported per ATP hydrolyzed, that ATP is hydrolyzed on the intracellular surface of the membrane, and that the concentrations of ATP, ADP, and Pi are 3 mM, 1 mM, and 0.5 mM, respectively. T = 298 K. What is the highest intracellular concentration of fructose that this transport system can generate Hint Kefer to Chapter 3 to recall the effects of concentration on free energy of ATP hydrolysis.)... 

In mimicking this type of function, noncyclic artificial carboxylic ionophores having two terminal groups of hydroxyl and carboxylic acid moieties were synthesized and the selective transport of alkali metal cations were examined by Yamazaki et al. 9 10). Noncyclic polyethers take on a pseudo-cyclic structure when coordinating cations and so it is possible to achieve the desired selectivity for specific cations by adjusting the length of the polyether chain 2). However, they were not able to observe any relationship between the selectivity and the structure of the host molecules in an active transport system using ionophores 1-3 10). (Table 1)... 

Fig. 9. Competitive transport of K+ and Na+ using ionophore 58 (Active transport system). (Cited from Ref.58>)...

A certain crown ether having additional coordination sites for a trasition metal cation (71) changes the transport property for alkali metal cations when it complexes with the transition metal cation 76) (Fig. 13). The fact that a carrier can be developed which has a reversible complexation property for a transition metal cation strongly suggests that this type of ionophore can be applied to the active transport system. 

This review surveys the types of host molecules that are applicable to the active transport system. It need scarcely be said that these results, which are based on selective transport in passive transport systems (see the Chaps. 3 and 5), strongly supports this consideration. From this point of view, a systematic investigation into the passive transport system as that by Izatt et al. is noted as one of the best approaches for clarifying the question of membrane transport77). 

Excretion via the kidney can be a straightforward question of glomerular filtration, followed by passage down the kidney tubules into the bladder. However, there can also be excretion and reabsorption across the tubular wall. This may happen if an ionized form within the tubule is converted into its nonpolar nonionized form because of a change in pH. The nonionized form can then diffuse across the tubular wall into plasma. Additionally, there are active transport systems for the excretion of lipophilic acids and bases across the wall of the proximal tubule. The antibiotic penicillin can be excreted in this way. 

Zhang EY, Phelps MA, Cheng C, Ekins S and Swaan PW. Modeling of active transport systems. Adv Drug Deliv Rev 2002 54 329-54. 

In the sarcoplasm of resting muscle, the concentration of Ca + is 10 to 10 mol/L. The resting state is achieved because Ca + is pumped into the sarcoplasmic reticulum through the action of an active transport system, called the Ca + ATPase (Figure 49-8), initiating relaxation. The sarcoplasmic reticulum is a network of fine membranous sacs. Inside the sarcoplasmic reticulum, Ca + is bound to a specific Ca -binding protein designated calsequestrin. The sarcomere is surrounded by an excitable membrane (the T tubule system) composed of transverse (T) channels closely associated with the sarcoplasmic reticulum. 

The galactose, arabinose and xylose transporters of E. coli The bacterium E. coli possesses at least 7 proton-linked, active transport systems for sugars (for a recent review see [212]). Three of these transporters, which catalyze the uptake of L-arabinose, D-xylose and D-galactose by symport with protons, are related in sequence to the sugar transporters discussed above. They probably represent the best-characterized of the non-mammalian transporters, and so are discussed here in some detail. 

Most biological reactions fall into the categories of first-order or second-order reactions, and we will discuss these in more detail below. In certain situations the rate of reaction is independent of reaction concentration hence the rate equation is simply v = k. Such reactions are said to be zero order. Systems for which the reaction rate can reach a maximum value under saturating reactant conditions become zero ordered at high reactant concentrations. Examples of such systems include enzyme-catalyzed reactions, receptor-ligand induced signal transduction, and cellular activated transport systems. Recall from Chapter 2, for example, that when [S] Ku for an enzyme-catalyzed reaction, the velocity is essentially constant and close to the value of Vmax. Under these substrate concentration conditions the enzyme reaction will appear to be zero order in the substrate. 

In microbes without a permeability barrier, or when the barrier fails, a mechanism must be in place to export metals from the cytoplasm. These active transport systems involve energy-dependent, membrane-bound efflux pumps that can be encoded by either chromosomal- or plasmid-borne genes. Active transport is the most well-studied metal resistance mechanism. Some of these include the ars operon for exporting arsenic from E. coli, the cad system for exporting cadmium from Staphylococcus aureus, and the cop operon for removing excess copper from Enterococcus hiraeP i9A0... 

Microbes that lack a specific active transport system for removing toxic metals may be able to sequester heavy metals either inside or outside of the cell. Intracellular sequestration occurs when cytoplasmic metal-binding molecules are produced in response to metal stress, preventing the metals from interacting with vital cell structures. The two most common molecules used for intracellular... 

Several active transport systems that are normally found in the small intestinal enterocytes have been characterized in the Caco-2 cell model [13]. These include transport systems for glucose [32, 33], amino acids [34-37], dipeptides [38-40], vitamins [41], and bile acids [42, 43]. 

The expression of the active transport systems is time-dependent and may vary with nutritional conditions [53, 54]. The culturing conditions, e.g., the passaging process, can dramatically alter the biological characteristics and transport properties of Caco-2 cell monolayers [55-58]. 

Mn2+ active transport system in Staphylococcus aureus. These metal-microbe interactions result in decrease microbial growth, abnormal morphological changes, and inhibition of biochemical processes in individual (Akmal et al. 2005a,b). The toxic effects of metals can be seen on a community level as well. In response to metal toxicity, overall community numbers and diversity decrease. Soil is a living system where all biochemical activities proceed through enzymatic processes. Heavy metals have also adverse effects on enzyme activities (Fig. 1). 

The answers are 333-c, 334-a, 335-d. (Katzung, pp 77-80. Hardman, pp 116, 132, 147—148.) Acetylcholine is synthesized from acetyl-CoA and choline. Choline is taken up into the neurons by an active transport system. Ilemicholinium blocks this uptake, depleting cellular choline, so that synthesis of ACh no longer occurs. 

Cells accumulate arsenic using an active transport system normally used in phosphate transport. 

Decreases Ca transport into cells, interferes with Ca -Na active transport system, increases renal tubular reabsorption of Ca and increases serum Ca and parathyroid concentrations ... 

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