Stress-induced evolution of Escherichia coli points to original concepts in respiratory cofactor selectivity

被引:38
作者
Auriol, Clement [1 ,2 ,3 ,4 ,5 ]
Bestel-Corre, Gwenaelle [6 ]
Claude, Jean-Baptiste [6 ]
Soucaille, Philippe [6 ]
Meynial-Salles, Isabelle [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Toulouse, F-31077 Toulouse, France
[2] Univ Toulouse 3, Inst Natl Sci Appl, Inst Natl Polytech, F-31077 Toulouse, France
[3] LISBP, F-31077 Toulouse, France
[4] Inst Natl Rech Agron, Ingn Syst Biol & Proc UMR792, F-31400 Toulouse, France
[5] Ctr Natl Rech Sci, UMR5504, F-31400 Toulouse, France
[6] Metab Explorer, Biopole Clermont Limagne, F-63360 St Beauzire, France
关键词
adaptive evolution; NADPH metabolism; complex I; OXIDOREDUCTASE COMPLEX-I; NADH DEHYDROGENASE FRAGMENT; LONG-TERM EXPERIMENT; TRANSHYDROGENASE; NUCLEOTIDES; METABOLISM; PATHWAY; SYSTEM; GROWTH; CHAIN;
D O I
10.1073/pnas.1010431108
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
Bacterial metabolism is characterized by a remarkable capacity to rapidly adapt to environmental changes. We restructured the central metabolic network in Escherichia coli to force a higher production of NADPH, and then grew this strain in conditions favoring adaptive evolution. A six-fold increase in growth capacity was attained that could be attributed in multiple clones, after whole genome mutation mapping, to a specific single mutation. Each clone had an evolved NuoF*(E183A) enzyme in the respiratory complex I that can now oxidize both NADH and NADPH. When a further strain was constructed with an even higher degree of NADPH stress such that growth was impossible on glucose mineral medium, a solid-state screening for mutations restoring growth, led to two different types of NuoF mutations in strains having recovered growth capacity. In addition to the previously seen E183A mutation other clones showed a E183G mutation, both having NADH and NADPH oxidizing ability. These results demonstrate the unique solution used by E. coli to overcome the NADPH stress problem. This solution creates a new function for NADPH that is no longer restricted to anabolic synthesis reactions but can now be also used to directly produce catabolic energy.
引用
收藏
页码:1278 / 1283
页数:6
相关论文
共 28 条
[1]   Characterization of the overproduced NADH dehydrogenase fragment of the NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli [J].
Braun, M ;
Bungert, S ;
Friedrich, T .
BIOCHEMISTRY, 1998, 37 (07) :1861-1867
[2]   One-step purification of the NADH dehydrogenase fragment of the Escherichia coli complex I by means of Strep-tag affinity chromatography [J].
Bungert, S ;
Krafft, B ;
Schlesinger, R ;
Friedrich, T .
FEBS LETTERS, 1999, 460 (02) :207-211
[3]  
Canonaco F, 2001, FEMS MICROBIOL LETT, V204, P247, DOI 10.1111/j.1574-6968.2001.tb10892.x
[4]   ANOMALOUS EFFECT OF UNCOUPLERS ON RESPIRATORY CHAIN-LINKED TRANSHYDROGENATION IN ESCHERICHIA-COLI MEMBRANES - EVIDENCE FOR A LOCALIZED PROTON PATHWAY [J].
CHANG, DYB ;
HOU, C ;
BRAGG, PD .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 293 (02) :246-253
[5]   Whole-genome resequencing of Escherichia coli K-12 MG1655 undergoing short-term laboratory evolution in lactate minimal media reveals flexible selection of adaptive mutations [J].
Conrad, Tom M. ;
Joyce, Andrew R. ;
Applebee, M. Kenyon ;
Barrett, Christian L. ;
Xie, Bin ;
Gao, Yuan ;
Palsson, Bernhard O. .
GENOME BIOLOGY, 2009, 10 (10)
[6]   One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products [J].
Datsenko, KA ;
Wanner, BL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6640-6645
[7]   Latent pathway activation and increased pathway capacity enable Escherichia coli adaptation to loss of key metabolic enzymes [J].
Fong, SS ;
Nanchen, A ;
Palsson, BO ;
Sauer, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (12) :8024-8033
[8]   A SMALL ISOFORM OF NADH-UBIQUINONE OXIDOREDUCTASE (COMPLEX-I) WITHOUT MITOCHONDRIALLY ENCODED SUBUNITS IS MADE IN CHLORAMPHENICOL-TREATED NEUROSPORA-CRASSA [J].
FRIEDRICH, T ;
HOFHAUS, G ;
ISE, W ;
NEHLS, U ;
SCHMITZ, B ;
WEISS, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 180 (01) :173-180
[9]   The NADH:ubiquinone oxidoreductase (complex I) from Escherichia coli [J].
Friedrich, T .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1364 (02) :134-146
[10]   Different Biochemical Mechanisms Ensure Network-Wide Balancing of Reducing Equivalents in Microbial Metabolism [J].
Fuhrer, Tobias ;
Sauer, Uwe .
JOURNAL OF BACTERIOLOGY, 2009, 191 (07) :2112-2121