Engineering Transport Protein Function: Theoretical and Technical Considerations Using the Sugar-Transporting Phosphotransferase System of Escherichia coli as a Model System

2006 ◽  
Vol 11 (6) ◽  
pp. 302-307 ◽  
Author(s):  
Xavier Soberón ◽  
Milton H. Saier Jr.
Genetics ◽  
1987 ◽  
Vol 115 (3) ◽  
pp. 419-429
Author(s):  
Maja Kricker ◽  
Barry G Hall

ABSTRACT The cellobiose catabolic system of Escherichia coli K12 is being used to study the role of cryptic genes in microbial evolution. Wild-type E. coli K12 do not utilize the β-glucoside sugars, arbutin, salicin and cellobiose. A Cel+ (cellobiose utilizing) mutant which grows on cellobiose, arbutin, and salicin was isolated previously from wild-type E. coli K12. Biochemical assays indicate that a cel structural gene (celT) specifies a single transport protein that is a β-glucoside specific enzyme of the phosphoenolpyruvate-dependent phosphotransferase system. The transport protein phosphorylates β-glucosides at the expense of phosphoenolpyruvate. A single phosphoglucosidase, specified by celH, hydrolyzes phosphorylated cellobiose, arbutin, and salicin. The genes of the cel system are expressed constitutively in the Cel+ mutant, whereas they are not expressed at a detectable level in the wild-type strain. The transport and hydrolase genes are simultaneously silenced or simultaneously expressed and thus constitute an operon. Cel+ strains which fail to utilize one or more β-glucosides express the transport system at a lower level than do Cel+ strains which grow on all three β-glucosides. Other strains inducibly express a gene which specifies transport of arbutin but not the other β-glucosides. The arbutin transport gene, arbT, maps outside of the cel locus.


1991 ◽  
Vol 266 (31) ◽  
pp. 20922-20927 ◽  
Author(s):  
K. Kashiwagi ◽  
T. Suzuki ◽  
F. Suzuki ◽  
T. Furuchi ◽  
H. Kobayashi ◽  
...  

1991 ◽  
Vol 266 (11) ◽  
pp. 6690-6692
Author(s):  
H H Pas ◽  
G H Meyer ◽  
W H Kruizinga ◽  
K S Tamminga ◽  
R P van Weeghel ◽  
...  

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