THE K-DRIVEN AMINO ACID COTRANSPORTER OF THE LARVAL MIDGUT OF LEPIDOPTERA: IS Na AN ALTERNATIVE SUBSTRATE?

نویسندگان

  • G. M. HANOZET
  • V. F. SACCHI
  • S. NEDERGAARD
  • P. BONFANTI
  • S. MAGAGNIN
چکیده

Amino acid accumulation within brush-border membrane vesicles (BBMV) from the larval midgut of Lepidoptera is driven by a K gradient. However, it can also be driven by a Na gradient, although with reduced efficiency. To examine the possibility that sodium and potassium ions are handled by the same amino acid transporter, glycine uptake into BBMV from Philosamia cynthia Drury was measured in the presence of a pH gradient and of a transmembrane electrical potential difference, i.e. in simulated 'physiological' conditions. The kinetics of glycine uptake at extravesicular saturating Na or K concentrations discloses a higher affinity of the cotransporter for the amino acid in the presence of Na but a maximum transport rate with K. Glycine uptake at a fixed concentration as a function of external Na or K concentration yields curves that show saturation but do not fit a rectangular hyperbola, with Hill coefficients less than 1 with Na and greater than 1 with K. These coefficients vary according to glycine concentration. Increasing the concentration of extravesicular Na at a saturating external K concentration reduced glycine uptake to 70% of the control value. This inhibition curve is compatible with competition between the two cations for the same cotransporter and with the presence of different kinetic constants with Na or K. The data are consistent with a steady-state random two-substrate mechanism for glycine transport, with Na and K as alternative substrates.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Molecular characteristics of mammalian and insect amino acid transporters: implications for amino acid homeostasis.

In mammalian cells, the uptake of amino acids is mediated by specialized, energy-dependent and passive transporters with overlapping substrate specificities. Most energy-dependent transporters are coupled either to the cotransport of Na+ or Cl- or to the countertransport of K+. Passive transporters are either facilitated transporters or channels. As a prelude to the molecular characterization o...

متن کامل

Cloning and characterization of a potassium-coupled amino acid transporter.

Active solute uptake in bacteria, fungi, plants, and animals is known to be mediated by cotransporters that are driven by Na+ or H+ gradients. The present work extends the Na+ and H+ dogma by including the H+ and K+ paradigm. Lepidopteran insect larvae have a high K+ and a low Na+ content, and their midgut cells lack Na+/K+ ATPase. Instead, an H+ translocating, vacuolar-type ATPase generates a ...

متن کامل

Anomalous glutamate/alkali cation symport in larval Manduca sexta midgut.

Rapid filtration assays were used to characterize glutamate/cation uptake in brush-border membrane vesicles from the larval midgut of the lepidopteran Manduca sexta. At pH 10.5, which is close to the physiological pH in the midgut of M. sexta, an inwardly directed K+ gradient stimulated glutamate uptake, suggesting that glutamate was symported. Gradients of Na+ or Li+ were less effective. Neith...

متن کامل

Cationic pathway of pH regulation in larvae of Anopheles gambiae.

Anopheles gambiae larvae (Diptera: Culicidae) live in freshwater with low Na(+) concentrations yet they use Na(+) for alkalinization of the alimentary canal, for electrophoretic amino acid uptake and for nerve function. The metabolic pathway by which larvae accomplish these functions has anionic and cationic components that interact and allow the larva to conserve Na(+) while excreting H(+) and...

متن کامل

K+ amino acid transporter KAAT1 mutant Y147F has increased transport activity and altered substrate selectivity.

KAAT1, a K(+)-coupled, neutral amino acid transporter from larval insect midgut, differs from other members of the Na(+):neurotransmitter transporter family (SNF) in two important ways: (1) it transports nutrient L-, alpha-amino acids, rather than neurotransmitters such as gamma-aminobutyric acid (GABA), and (2) it accepts K(+) as well as Na(+) as a co-substrate. To determine whether the restor...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2005