Characterization and Molecular Mechanism of AroP as an Aromatic Amino Acid and Histidine Transporter in Corynebacterium glutamicum

• Published in: Journal of Bacteriology Vol. 195; no. 23; pp. 5334 - 5342
• Main Authors: Shang, Xiuling, Zhang, Yun, Zhang, Guoqiang, Chai, Xin, Deng, Aihua, Liang, Yong, Wen, Tingyi
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.12.2013
• Subjects: Amino Acid Transport Systems - genetics; Amino Acid Transport Systems - metabolism; amino acid transporters; Amino acids; Amino Acids - metabolism; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacteriology; Binding sites; Biosynthesis; Correlation analysis; Corynebacterium glutamicum; Corynebacterium glutamicum - genetics; Corynebacterium glutamicum - metabolism; energy; Gene Expression Regulation, Bacterial - physiology; Gram-positive bacteria; histidine; hydrophobic bonding; missense mutation; Models, Molecular; phenylalanine; Phylogeny; Protein Binding; Protein Conformation; Substrates; tryptophan; tyrosine
• ISSN: 0021-9193; 1098-5530; 1067-8832
• DOI: 10.1128/jb.00971-13

Corynebacterium glutamicum is equipped with abundant membrane transporters to adapt to a changing environment. Many amino acid transporters have been identified in C. glutamicum, but histidine uptake has not been investigated in detail. Here, we identified the aromatic amino acid transporter encoded by aroP as a histidine transporter in C. glutamicum by a combination of the growth and histidine uptake features. Characterization of histidine uptake showed that AroP has a moderate affinity for histidine, with a Km value of 11.40 ± 2.03 μM, and histidine uptake by AroP is competitively inhibited by the aromatic amino acids. Among the four substrates, AroP exhibits a stronger preference for tryptophan than for tyrosine, phenylalanine, and histidine. Homology structure modeling and molecular docking were performed to predict the substrate binding modes and conformational changes during substrate transport. These results suggested that tryptophan is best accommodated in the binding pocket due to shape compatibility, strong hydrophobic interactions, and the lowest binding energy, which is consistent with the observed substrate preference of AroP. Furthermore, the missense mutations of the putative substrate binding sites verified that Ser24, Ala28, and Gly29 play crucial roles in substrate binding and are highly conserved in the Gram-positive bacteria. Finally, the expression of aroP is not significantly affected by extracellular histidine or aromatic amino acids, indicating that the physiological role of AroP may be correlated with the increased fitness of C. glutamicum to assimilate extracellular amino acid for avoiding the high energy cost of amino acid biosynthesis.