Emergent properties of reduced-genome Escherichia coli

被引:522
作者
Pósfai, G
Plunkett, G
Fehér, T
Frisch, D
Keil, GM
Umenhoffer, K
Kolisnychenko, V
Stahl, B
Sharma, SS
de Arruda, M
Burland, V
Harcum, SW
Blattner, FR
机构
[1] Biol Res Ctr, Inst Biochem, H-6726 Szeged, Hungary
[2] Scarab Genom LLC, Madison, WI 53713 USA
[3] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
[4] Univ Wisconsin, Genome Ctr Wisconsin, Madison, WI 53706 USA
[5] Friedrich Loeffler Inst, Inst Mol Biol, Fed Res Ctr Virus Dis Anim, D-17493 Greifswald, Germany
[6] Clemson Univ, Dept Chem & Biomol Engn, Clemson, SC 29634 USA
[7] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
关键词
D O I
10.1126/science.1126439
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the use of synthetic biology, we reduced the Escherichia coli K-12 genome by making planned, precise deletions. The multiple-deletion series (MDS) strains, with genome reductions up to 15%, were designed by identifying nonessential genes and sequences for elimination, including recombinogenic or mobile DNA and cryptic virulence genes, while preserving good growth profiles and protein production. Genome reduction also led to unanticipated beneficial properties: high electroporation efficiency and accurate propagation of recombinant genes and plasmids that were unstable in other strains. Eradication of stress-induced transposition evidently stabilized the MDS genomes and provided some of the new properties.
引用
收藏
页码:1044 / 1046
页数:3
相关论文
共 19 条
[11]   Engineering a reduced Escherichia coli genome [J].
Kolisnychenko, V ;
Plunkett, G ;
Herring, CD ;
Fehér, T ;
Pósfai, J ;
Blattner, FR ;
Pósfai, G .
GENOME RESEARCH, 2002, 12 (04) :640-647
[12]   RABBIT HEMORRHAGIC-DISEASE VIRUS - MOLECULAR-CLONING AND NUCLEOTIDE SEQUENCING OF A CALICIVIRUS GENOME [J].
MEYERS, G ;
WIRBLICH, C ;
THIEL, HJ .
VIROLOGY, 1991, 184 (02) :664-676
[13]   Escherichia coli K-12:: a cooperatively developed annotation snapshot -: 2005 [J].
Riley, M ;
Abe, T ;
Arnaud, MB ;
Berlyn, MKB ;
Blattner, FR ;
Chaudhuri, RR ;
Glasner, JD ;
Horiuchi, T ;
Keseler, IM ;
Kosuge, T ;
Mori, H ;
Perna, NT ;
Plunkett, G ;
Rudd, KE ;
Serres, MH ;
Thomas, GH ;
Thomson, NR ;
Wishart, D ;
Wanner, BL .
NUCLEIC ACIDS RESEARCH, 2006, 34 (01) :1-9
[14]   MAPPING OF A D-CYCLOSERINE RESISTANCE LOCUS IN ESCHERICHIA-COLI K-12 [J].
RUSSELL, RRB .
JOURNAL OF BACTERIOLOGY, 1972, 111 (02) :622-&
[15]   Recombinant AAV2 transduction of primitive human hematopoietic stem cells capable of serial engraftment in immune-deficient mice [J].
Santat, L ;
Paz, H ;
Wong, C ;
Li, LJ ;
Macer, J ;
Forman, S ;
Wong, KK ;
Chatterjee, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (31) :11053-11058
[16]   Isolation and characterization of IS1 circles [J].
Sekine, Y ;
Eisaki, N ;
Kobayashi, K ;
Ohtsubo, E .
GENE, 1997, 191 (02) :183-190
[17]   GenProtEC:: an updated and improved analysis of functions of Escherichia coli K-12 proteins [J].
Serres, MH ;
Goswami, S ;
Riley, M .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D300-D302
[18]   MECHANISM OF D-CYCLOSERINE ACTION - TRANSPORT MUTANTS FOR D-ALANINE, D-CYCLOSERINE, AND GLYCINE [J].
WARGEL, RJ ;
SHADUR, CA ;
NEUHAUS, FC .
JOURNAL OF BACTERIOLOGY, 1971, 105 (03) :1028-&
[19]   Minimization of the Escherichia coli genome using a Tn5-targeted Cre/loxP excision system [J].
Yu, BJ ;
Sung, BH ;
Koob, MD ;
Lee, CH ;
Lee, JH ;
Lee, WS ;
Kim, MS ;
Kim, SC .
NATURE BIOTECHNOLOGY, 2002, 20 (10) :1018-1023