Abstract

A comprehensive proteomic study was carried out to identify and characterize proteins expressed by Bifidobacterium longum NCC2705. A total of 708 spots representing 369 protein entries were identified by MALDI-TOF-MS and/or ESI-MS/MS. Isoelectric point values estimated by gel electrophoresis matched closely with their predicted ones, although some discrepancies exist suggesting that post-translational protein modifications might be common in B. longum. The identified proteins represent 21.4% of the predicted 1727 ORFs in the genome and correspond to 30% of the predicted proteome. Moreover 95 hypothetical proteins were experimentally identified. This is the first compilation of a proteomic reference map for the important probiotic organism B. longum NCC2705. The study aimed to define a number of cellular pathways related to important physiological processes at the proteomic level. Proteomic comparison of glucose- and fructose-grown cells revealed that fructose and glucose are catabolized via the same degradation pathway. Interestingly the sugar-binding protein specific to fructose (BL0033) and Frk showed higher levels of expression in cells grown on fructose than on glucose as determined by semiquantitative RT-PCR. BL0033 time course and concentration experiments showed that the induction time and fructose concentration correlates to increased expression of BL0033. At the same time, an ABC (ATP-binding cassette) transporter ATP-binding protein (BL0034) was slightly up-regulated in cells grown on fructose compared with glucose. All of the above results suggest that the uptake of fructose into the cell may be conducted by a specific transport system in which BL0033 might play an important role.

Highlights

  • A comprehensive proteomic study was carried out to identify and characterize proteins expressed by Bifidobacterium longum NCC2705

  • After analyzing homology to sequences in GenBankTM using the Basic Local Alignment Search Tool (BLAST) available on the National Center for Biotechnology Information server, we found that the xfp sequences from B. longum NCC2705 and ATCC15707 are very similar to the 10 xfp coding sequences from other bifidobacteria

  • To identify the catabolic route allowing D-fructose fermentation, we first compared the proteomic profile of B. longum strain NCC2705 grown on fructose or glucose

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Summary

Introduction

A comprehensive proteomic study was carried out to identify and characterize proteins expressed by Bifidobacterium longum NCC2705. In this study we focused on generating a base-line signature or cartographic reference of the B. longum strain NCC2705 proteome by identifying ORF expression and investigating the mechanism of fructose translocation, uptake, and utilization. To study the regulation and expression of the gene coding for the enzyme, we cloned and sequenced the ORF (2475 bp; 825 amino acids) from B. longum NCC2705 and ATCC15707.

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