The phrase "adapt protein expression" is correct and usable in written English.
It can be used in scientific or research contexts, particularly in molecular biology or biochemistry, to refer to the modification or alteration of how proteins are produced in an organism or system.
Example: "Researchers are exploring ways to adapt protein expression in yeast to enhance the production of therapeutic proteins."
Alternatives: "modify protein expression" or "alter protein expression".
Hence, positive selection of the β-xylosidase gene could reflect functional optimization resulting in the expression of a biochemically better adapted protein, for example by altering its hydrolytic activity.
Unlike ICM cells however, ESCs are adapted to culture; protein expression is also interchangeable among cells in a given ESC culture and is associated with dynamic changes in histone modifications [7].
Many pathogens undergo significant changes in their gene and protein expression to adapt to growth in iron limiting conditions, including Francisella tularensis, Mycobacterium tuberculosis, and Streptococcus pneumoniae [12], [13], [14].
We adapted and optimized the protocol for protein expression by Y. lipolytica in 96-well microplates.
Attributed to the significant increase in mRNA abundance and protein expression level observed in adapted S. cerevisiae under stress challenge, the NADPH-dependent oxidoreductases ADH7p and YKL071Wp were found to be responsible for furfural detoxification [ 15, 16].
Another approach to obtain GFP-tagged protein expression is recombineering, a protocol adapted for C. elegans by Dolphin and Hope [48] and Sarov et al. [49].
Support for these statements is found in the observation that chronic consumption of alcohol induces long-term changes in brain gene and protein expression, which allow brain cells to adapt through homeostatic alterations in distinct signaling pathways [ 3, 4].
In this paper we look at the role of genetic determination versus plastic response by comparing the protein expression profiles between two sympatric ecotypes adapted to different shore levels and habitats using two-dimensional protein maps.
In addition to the direct effects of DCA on PDK inhibition, many changes in gene and protein expression could occurred in these time frames as the cells adapt to the presence of DCA over time.
Accordingly, in this study we report the use of synthetic genes designed from the published amino acid sequence of the mature bacteriocins SRCAM 602, OR-7, E-760, and L-1077 and with adapted codon usage for expression by P. pastoris, their cloning into the protein expression vector pPICZ αA, and their expression by recombinant P. pastoris X-33.
