TY - JOUR
T1 - Escherichia coli yjjPB genes encode a succinate transporter important for succinate production
AU - Fukui, Keita
AU - Nanatani, Kei
AU - Hara, Yoshihiko
AU - Yamakami, Suguru
AU - Yahagi, Daiki
AU - Chinen, Akito
AU - Tokura, Mitsunori
AU - Abe, Keietsu
N1 - Publisher Copyright:
© 2017 Japan Society for Bioscience, Biotechnology, and Agrochemistry.
PY - 2017
Y1 - 2017
N2 - Under anaerobic conditions, Escherichia coli produces succinate from glucose via the reductive tricarboxylic acid cycle. To date, however, no genes encoding succinate exporters have been established in E. coli. Therefore, we attempted to identify genes encoding succinate exporters by screening an E. coli MG1655 genome library. We identified the yjjPB genes as candidates encoding a succinate transporter, which enhanced succinate production in Pantoea ananatis under aerobic conditions. A complementation assay conducted in Corynebacterium glutamicum strain AJ110655ΔsucE1 demonstrated that both YjjP and YjjB are required for the restoration of succinate production. Furthermore, deletion of yjjPB decreased succinate production in E. coli by 70% under anaerobic conditions. Taken together, these results suggest that YjjPB constitutes a succinate transporter in E. coli and that the products of both genes are required for succinate export.
AB - Under anaerobic conditions, Escherichia coli produces succinate from glucose via the reductive tricarboxylic acid cycle. To date, however, no genes encoding succinate exporters have been established in E. coli. Therefore, we attempted to identify genes encoding succinate exporters by screening an E. coli MG1655 genome library. We identified the yjjPB genes as candidates encoding a succinate transporter, which enhanced succinate production in Pantoea ananatis under aerobic conditions. A complementation assay conducted in Corynebacterium glutamicum strain AJ110655ΔsucE1 demonstrated that both YjjP and YjjB are required for the restoration of succinate production. Furthermore, deletion of yjjPB decreased succinate production in E. coli by 70% under anaerobic conditions. Taken together, these results suggest that YjjPB constitutes a succinate transporter in E. coli and that the products of both genes are required for succinate export.
KW - Aerobic conditions
KW - Anaerobic conditions
KW - Escherichia coli
KW - Succinate production
KW - Succinate transporter
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U2 - 10.1080/09168451.2017.1345612
DO - 10.1080/09168451.2017.1345612
M3 - Article
C2 - 28673128
AN - SCOPUS:85026919270
SN - 0916-8451
VL - 81
SP - 1837
EP - 1844
JO - Bioscience, Biotechnology and Biochemistry
JF - Bioscience, Biotechnology and Biochemistry
IS - 9
ER -