TY - JOUR
T1 - Vibrio natriegens as host for expression of multisubunit membrane protein complexes
AU - Schleicher, Lena
AU - Muras, Valentin
AU - Claussen, Björn
AU - Pfannstiel, Jens
AU - Blombach, Bastian
AU - Dibrov, Pavel
AU - Fritz, Günter
AU - Steuber, Julia
N1 - Publisher Copyright:
© 2018 Frontiers Media S.A. All rights reserved.
PY - 2018/10/25
Y1 - 2018/10/25
N2 - Escherichia coli is a convenient host for the expression of proteins, but the heterologous production of large membrane protein complexes often is hampered by the lack of specific accessory genes required for membrane insertion or cofactor assembly. In this study we introduce the non-pathogenic and fast-growing Vibrio natriegens as a suitable expression host for membrane-bound proteins from Vibrio cholerae. We achieved production of the primary Na+ pump, the NADH:quinone oxidoreductase (NQR), from V. cholerae in an active state, as indicated by increased overall NADH:quinone oxidoreduction activity of membranes from the transformed V. natriegens, and the sensitivity toward Ag+, a specific inhibitor of the NQR. Complete assembly of V. cholerae NQR expressed in V. natriegens was demonstrated by BN PAGE followed by activity staining. The secondary transport system Mrp from V. cholerae, another membrane-bound multisubunit complex, was also produced in V. natriegens in a functional state, as demonstrated by in vivo Li+ transport. V. natriegens is a promising expression host for the production of membrane protein complexes from Gram-negative pathogens.
AB - Escherichia coli is a convenient host for the expression of proteins, but the heterologous production of large membrane protein complexes often is hampered by the lack of specific accessory genes required for membrane insertion or cofactor assembly. In this study we introduce the non-pathogenic and fast-growing Vibrio natriegens as a suitable expression host for membrane-bound proteins from Vibrio cholerae. We achieved production of the primary Na+ pump, the NADH:quinone oxidoreductase (NQR), from V. cholerae in an active state, as indicated by increased overall NADH:quinone oxidoreduction activity of membranes from the transformed V. natriegens, and the sensitivity toward Ag+, a specific inhibitor of the NQR. Complete assembly of V. cholerae NQR expressed in V. natriegens was demonstrated by BN PAGE followed by activity staining. The secondary transport system Mrp from V. cholerae, another membrane-bound multisubunit complex, was also produced in V. natriegens in a functional state, as demonstrated by in vivo Li+ transport. V. natriegens is a promising expression host for the production of membrane protein complexes from Gram-negative pathogens.
KW - Expression
KW - Membrane proteins
KW - Multiple resistance and pH related antiporter
KW - Multisubunit complexes
KW - Na-translocating NADH:quinone oxidoreductase
KW - Strep-Tag
KW - Vibrio natriegens
UR - http://www.scopus.com/inward/record.url?scp=85055774723&partnerID=8YFLogxK
U2 - 10.3389/fmicb.2018.02537
DO - 10.3389/fmicb.2018.02537
M3 - Article
AN - SCOPUS:85055774723
SN - 1664-302X
VL - 9
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
IS - OCT
M1 - 2537
ER -