TY - JOUR
T1 - Adaptive evolution of a minimal organism with a synthetic genome
AU - Sandberg, Troy E.
AU - Wise, Kim S.
AU - Dalldorf, Christopher
AU - Szubin, Richard
AU - Feist, Adam M.
AU - Glass, John I.
AU - Palsson, Bernhard O.
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023
Y1 - 2023
N2 - The bacterial strain JCVI-syn3.0 stands as the first example of a living organism with a minimized synthetic genome, derived from the Mycoplasma mycoides genome and chemically synthesized in vitro.
Here, we report the experimental evolution of a syn3.0- derived strain.
Ten independent replicates were evolved for several hundred
generations, leading to growth rate improvements of > 15%. Endpoint
strains possessed an average of 8 mutations composed of indels and SNPs, with a pronounced C/G- > A/T transversion bias. Multiple genes were repeated mutational targets across the independent lineages, including phase variable lipoprotein activation, 5 distinct; nonsynonymous substitutions in the same membrane transporter protein, and inactivation of an uncharacterized gene. Transcriptomic analysis revealed an overall tradeoff reflected in upregulated ribosomal proteins and downregulated DNA and RNA
related proteins during adaptation. This work establishes the
suitability of synthetic, minimal strains for laboratory evolution,
providing a means to optimize strain growth characteristics and
elucidate gene functionality.
AB - The bacterial strain JCVI-syn3.0 stands as the first example of a living organism with a minimized synthetic genome, derived from the Mycoplasma mycoides genome and chemically synthesized in vitro.
Here, we report the experimental evolution of a syn3.0- derived strain.
Ten independent replicates were evolved for several hundred
generations, leading to growth rate improvements of > 15%. Endpoint
strains possessed an average of 8 mutations composed of indels and SNPs, with a pronounced C/G- > A/T transversion bias. Multiple genes were repeated mutational targets across the independent lineages, including phase variable lipoprotein activation, 5 distinct; nonsynonymous substitutions in the same membrane transporter protein, and inactivation of an uncharacterized gene. Transcriptomic analysis revealed an overall tradeoff reflected in upregulated ribosomal proteins and downregulated DNA and RNA
related proteins during adaptation. This work establishes the
suitability of synthetic, minimal strains for laboratory evolution,
providing a means to optimize strain growth characteristics and
elucidate gene functionality.
U2 - 10.1016/j.isci.2023.107500
DO - 10.1016/j.isci.2023.107500
M3 - Journal article
C2 - 37636038
AN - SCOPUS:85167810571
SN - 2589-0042
VL - 26
JO - iScience
JF - iScience
IS - 9
M1 - 107500
ER -