## Abstract Two nucleoside transport systems have been verified and separated by mating and recombination experiments. The recipient strain was a mutant which is negative for transport of all nucleosides. The two systems differ in specificity and in regulation. One system transports pyrimidine and
Expression and regulation of protein K, an Escherichia coli K1 porin, in Escherichia coli K-12
β Scribed by Joyce A. Sutcliffe; John D. Foulds
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 576 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
β¦ Synopsis
Using a modified lambda phage as a vector and a procedure developed in Dr. C. Schnaitman's laboratory, we have cloned the structural gene for protein K from an Escherichia coli K1 strain to an E coli K-12 strain. The cloned inserts consist of two HindIII fragments, 4 kb and 6.5 kb in size. The protein produced by the insert is nearly identical to "authentic" protein K when chymotryptic peptides of 125I-labeled proteins are compared. Protein K was found to respond to changes in the osmolarity of the medium, being favored in trypticase soy broth (high osmolarity). This fluctuation was not dependent on a functional ompR gene. However, protein K was not expressed in strains carrying the envZ-473 mutation. Thus, protein K appears to be within a class of exported proteins whose expression is regulated by the envZ gene independent of the ompR gene.
π SIMILAR VOLUMES
Streptothricin acetyl transferase coded for byplasmidspIE636 andpIE637 in Escherichia coli K-12 was found to be located at the inner side of the cytoplasmic membrane.
## Cell immobilization induces changes in the protein response of Escherichia coli K-12 to a cold shock We have compared the protein expression of gel-entrapped Escherichia coli cells submitted to a cold shock at 47C with those of exponential-and stationary-phase freefloating counterparts. Autorad