Abstract

BackgroundIt is well known that peptides play a vital role in the nutrition and health of dairy cows. Bovine oligopeptide transporter 1 (bPepT1) is involved in the peptide transport process in the gastrointestinal tracts of dairy cows. However, little information is known in the characteristics of bPepT1. Therefore, the purpose of this study was to characterize bPepT1 functionally using a mammalian cell expression system. The uptake of radiolabeled dipeptide glycyl-sarcosine ([3H]-Gly-Sar) into the bPepT1-transfected Chinese hamster ovary cells was measured at various pH and substrate concentrations and with or without 15 other small peptides that contained Met or Lys.ResultsWestern blot results showed that the abundance of bPepT1 protein in the jejunum and ileum are the highest in the gastrointestinal tract of dairy cows. The uptake of [3H]-Gly-Sar by bPepT1-Chinese hamster ovary cells was dependent on time, pH, and substrate concentration, with a low Km value of 0.94 ± 0.06 mmol/L and a maximum velocity of 20.80 ± 1.74 nmol/(mg protein • 5 min). Most of the di- and tripeptides were the substrates of bPepT1, based on substrate-competitive studies. However, bPepT1 has a higher affinity to the peptides with shorter chains, greater hydrophobicity, and negative or neutral charges.ConclusionsThese results demonstrated for the first time the functional characteristics of bPepT1, and they provide a new insight and better understanding into its vital role in absorbing a wide range of peptides from the digestive tract of dairy cows.

Highlights

  • It is well known that peptides play a vital role in the nutrition and health of dairy cows

  • These results demonstrated for the first time the functional characteristics of Bovine oligopeptide transporter 1 (bPepT1), and they provide a new insight and better understanding into its vital role in absorbing a wide range of peptides from the digestive tract of dairy cows

  • The hydropathy analysis predicted that bPepT1 has 12 potential transmembrane domains (TMD), with a large extracellular loop between TMD 9 and 10 (Fig. 1)

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Summary

Introduction

It is well known that peptides play a vital role in the nutrition and health of dairy cows. Bovine oligopeptide transporter 1 (bPepT1) is involved in the peptide transport process in the gastrointestinal tracts of dairy cows. The uptake of radiolabeled dipeptide glycyl-sarcosine ([3H]-Gly-Sar) into the bPepT1-transfected Chinese hamster ovary cells was measured at various pH and substrate concentrations and with or without 15 other small peptides that contained Met or Lys. Peptide absorption from gastrointestinal lumen plays an important role in protein nutrition and health of animals [1, 2]. The oligopeptide transporter 1 (PepT1) plays a vital role in mediating the uptake of a fraction of dietary AA in the form of small peptides [1, 2]. There are few reports on the PepT1 expression profile and kinetics in dairy cows

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