Related Experiment Video
Updated: Jan 2, 2026

A Protocol for Functional Assessment of Whole-Protein Saturation Mutagenesis Libraries Utilizing High-Throughput Sequencing
Published on: July 3, 2016
Mutations that improve efficiency of a weak-link enzyme are rare compared to adaptive mutations elsewhere in the
Andrew B Morgenthaler1,2, Wallis R Kinney1,2, Christopher C Ebmeier1
1Department of Molecular, Cellular, and Developmental Biology, University of Colorado Boulder, Boulder, United States.
Abstract:
New enzymes often evolve by gene amplification and divergence. Previous experimental studies have followed the evolutionary trajectory of an amplified gene, but have not considered mutations elsewhere in the genome when fitness is limited by an evolving gene. We have evolved a strain of Escherichia coli in which a secondary promiscuous activity has been recruited to serve an essential function. The gene encoding the 'weak-link' enzyme amplified in all eight populations, but mutations improving the newly needed activity occurred in only one. Most adaptive mutations occurred elsewhere in the genome. Some mutations increase expression of the enzyme upstream of the weak-link enzyme, pushing material through the dysfunctional metabolic pathway. Others enhance production of a co-substrate for a downstream enzyme, thereby pulling material through the pathway. Most of these latter mutations are detrimental in wild-type E. coli, and thus would require reversion or compensation once a sufficient new activity has evolved.
Related Concept Videos
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair
Mutations in Microorganisms
Gene Evolution - Fast or Slow?
In contrast, regions which code...
Genome Copying Errors
Catalytically Perfect Enzymes
Most enzymes...

