Metabolic
engineering and synthetic biology have been applied for the discovery and
redesign of the potentials of microorganisms for numerous desired purposes.
Both model hosting strains and microorganisms with highly-specific functionshave been engineered to improve feedstock utilization, target fuel and chemical
production, as well as regulate cellular physiology. For instance, the baker’s
yeast, Saccharomyces cerevisiae, which was first used by the human society
thousands of years ago, has been genetically engineered to ferment otherwise
non-fermentable carbon sources. Indeed, C5 sugars such as xylose cannot
natively be catabolized by S. cerevisiae.
However, the engineered S. cerevisiae
strains are able to metabolize xylose efficiently and to produce ethanol. Theengineered microbes could simultatneously co-ferment carbon in the hydrolysateof lignocellulosic biomass such as hemicellulose- and cellulose-derived C5/C6
sugars and lignin-derived aromatics and produce fuels and value-added chemicals
such as ethanol, n-butanol, sesquiterpenes, polyhydroxyalkanoates (PHA), and
fatty acid ethyl esters. These advances are not limited to model hosts, such as
S. cerevisiae and Escherichia coli, but have also been demonstrated in
Clostridium acetobutylicum, Bacillus subtilis, Pseudomonas putida, and
Synechococcus elongatus.
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