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• W1568276439 endingPage "9201" @default.
• W1568276439 startingPage "9194" @default.
• W1568276439 abstract "The Pseudomonas oleovorans alkane hydroxylase is an integral cytoplasmic membrane protein that is expressed and active in both Escherichia coli and P. oleovorans. Its primary sequence contains eight hydrophobic stretches that could span the membrane as alpha-helices. The topology of alkane hydroxylase was studied in E. coli using protein fusions linking different amino-terminal fragments of the alkane hydroxylase (AlkB) to alkaline phosphatase (PhoA) and to beta-galactosidase (LacZ). Four AlkB-PhoA fusions were constructed using transposon TnphoA. Site-directed mutagenesis was used to create PstI sites at 12 positions in AlkB. These sites were used to create AlkB-PhoA and AlkB-LacZ fusions. With respect to alkaline phosphatase and beta-galactosidase activity each set of AlkB-PhoA and AlkB-LacZ fusions revealed the expected complementary activities. At three positions, PhoA fusions were highly active, whereas the corresponding LacZ fusions were the least active. At all other positions the PhoA fusions were almost completely inactive, but the corresponding LacZ fusions were highly active. These data predict a model for alkane hydroxylase containing six transmembrane segments. In this model the amino terminus, two hydrophilic loops, and a large carboxyl-terminal domain are located in the cytoplasm. Only three very short loops near amino acid positions 52, 112, and 251 are exposed to the periplasm." @default.
• W1568276439 created "2016-06-24" @default.
• W1568276439 creator A5017919633 @default.
• W1568276439 creator A5050315364 @default.
• W1568276439 creator A5054688355 @default.
• W1568276439 date "1992-05-01" @default.
• W1568276439 modified "2023-10-13" @default.
• W1568276439 title "Topology of the membrane-bound alkane hydroxylase of Pseudomonas oleovorans." @default.
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• W1568276439 doi "https://doi.org/10.1016/s0021-9258(19)50407-0" @default.
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• W1568276439 hasPublicationYear "1992" @default.
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