Article ID Journal Published Year Pages File Type
10871387 FEBS Letters 2012 7 Pages PDF
Abstract
► We produced an improved system for production of recombinant phosphoproteins in Escherichia coli. ► Genome modification and strain engineering of E. coli enabled RF1 deletion. ► Single and double phosphoserine residues were incorporated into recombinant proteins at enhanced efficiency. ► Phosphoserine insertion at native UAG sites reduces cellular fitness and viability.
Related Topics
Life Sciences Agricultural and Biological Sciences Plant Science
Authors
, , , , , , , , , ,