Erratum: Growth of E. coli BL21 in minimal media with different gluconeogenic carbon sources and salt contents (Applied Microbiology and Biotechnology DOI: 10.1007/s00253-006-0554-8);Growth of E. coli BL21 in minimal media with different gluconeogenic carbon sources and salt contents

Applied Microbiology and Biotechnology

Volumn 73, Issue 5, 2007, Pages 1169-1172

  Paliy, Oleg ^a   Gunasekera, Thusitha S ^a  

^a WRIGHT STATE UNIVERSITY   (United States)

Author keywords

Acetate; BL21; Escherichia coli; Gluconeogenesis; Minimal medium; Succinate

Indexed keywords

CARBON; CELL CULTURE; DEUTERIUM COMPOUNDS; ISOTOPES; PROTEINS; PURIFICATION;

ACETATE; BL21; GLUCONEOGENESIS; MINIMAL MEDIUM; SUCCINATE;

ESCHERICHIA COLI;

ACETIC ACID; CARBON; FERROUS SULFATE; FUMARIC ACID; GLYCEROL; PYRUVIC ACID; SODIUM CHLORIDE; SUCCINIC ACID;

ACETATE; COLIFORM BACTERIUM; GROWTH CURVE; GROWTH RATE; NUTRITION; ORGANIC ACID; SALT; SUBSTRATE;

ARTICLE; BACTERIAL CELL; BACTERIAL GROWTH; BACTERIAL STRAIN; BACTERIUM CULTURE; CELL DENSITY; CHEMICAL COMPOSITION; CONTROLLED STUDY; CULTURE MEDIUM; ESCHERICHIA COLI; GLUCONEOGENESIS; GROWTH RATE; NONHUMAN; WILD TYPE;

ESCHERICHIA COLI;

EID: 33845779493     PISSN: 01757598     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00253-006-0683-0     Document Type: Erratum

References (22)

1. Andersen KB, von Meyenburg K (1980) Are growth rates of Escherichia coli in batch cultures limited by respiration? J Bacteriol 144(1):114-123
2. Bhandari P, Gowrishankar J (1997) An Escherichia coli host strain useful for efficient overproduction of cloned gene products with NaCl as the inducer. J Bacteriol 179(13):4403-4406
3. Boogerd FC, Boe L, Michelsen O, Jensen PR (1998) atp mutants of Escherichia coli fail to grow on succinate due to a transport deficiency. J Bacteriol 180(22):5855-5859
4. Gardner KH, Kay LE (1998) The use of 2H, 13C, 15N multidimensional NMR to study the structure and dynamics of proteins. Annu Rev Biophys Biomol Struct 27:357-406
5. Gilsdorf J, Gul N, Smith LA (2006) Expression, purification, and characterization of Clostridium botulinum type B light chain. Protein Expr Purif 46(2):256-267
6. Gutnick D, Calvo JM, Klopotowski T, Ames BN (1969) Compounds which serve as the sole source of carbon or nitrogen for Salmonella typhimurium LT-2. J Bacteriol 100(1):215-219
7. Gyaneshwar P, Paliy O, McAuliffe J, Popham DL, Jordan MI, Kustu S (2005) Sulfur and nitrogen limitation in Escherichia coli K-12: specific homeostatic responses. J Bacteriol 187(3):1074-1090
8. Lee SK, Keasling JD (2006) Propionate-regulated high-yield protein production in Escherichia coli. Biotechnol Bioeng 93(5):912-918
9. LeMaster DM (1990) Deuterium labelling in NMR structural analysis of larger proteins. Q Rev Biophys 23(2):133-174
10. LeMaster DM, Richards FM (1982) Preparative-scale isolation of isotopically labeled amino acids. Anal Biochem 122(2):238-247
11. LeMaster DM, Richards FM (1988) NMR sequential assignment of Escherichia coli thioredoxin utilizing random fractional deuteriation. Biochemistry 27(1):142-150
12. Paliy O, Bloor D, Brockwell D, Gilbert P, Barber J (2003) Improved methods of cultivation and production of deuteriated proteins from E. coli strains grown on fully deuteriated minimal medium. J Appl Microbiol 94(4):580-586
13. Phue JN, Shiloach J (2004) Transcription levels of key metabolic genes are the cause for different glucose utilization pathways in E. coli B (BL21) and E. coli K (JM109). J Biotechnol 109(1-2):21-30
14. Phue JN, Noronha SB, Hattacharyya R, Wolfe AJ, Shiloach J (2005) Glucose metabolism at high density growth of E. coli B and E. coli K: differences in metabolic pathways are responsible for efficient glucose utilization in E. coli B as determined by microarrays and Northern blot analyses. Biotechnol Bioeng 90(7):805-820
15. Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
16. Sosa-Peinado A, Mustafi D, Makinen MW (2000) Overexpression and biosynthetic deuterium enrichment of TEM-1 beta-lactamase for structural characterization by magnetic resonance methods. Protein Expr Purif 19(2):235-245
17. Soupene E, van Heeswijk WC, Plumbridge J, Stewart V, Bertenthal D, Lee H, Prasad G, Paliy O, Charernnoppakul P, Kustu S (2003) Physiological studies of Escherichia coli strain MG1655: growth defects and apparent cross-regulation of gene expression. J Bacteriol 185(18):5611-5626
18. Tuominen VU, Myles DA, Dauvergne MT, Lahti R, Heikinheimo P, Goldman A (2004) Production and preliminary analysis of perdeuterated yeast inorganic pyrophosphatase crystals suitable for neutron diffraction. Acta Crystallogr D Biol Crystallogr 60(Pt 3):606-609
19. Vanatalu K, Paalme T, Vilu R, Burkhardt N, Junemann R, May R, Ruhl M, Wadzack J, Nierhaus KH (1993) Large-scale preparation of fully deuterated cell components. Ribosomes from Escherichia coli with high biological activity. Eur J Biochem 216(1):315-321
20. Yadava RS, Kumar R, Yadava PK (2005) Expression of lexA targeted ribozyme in Escherichia coli BL-21 (DE3) cells. Mol Cell Biochem 271(1-2):197-203
21. Zhang Z, Gosset G, Barabote R, Gonzalez CS, Cuevas WA, Saier MH Jr (2005) Functional interactions between the carbon and iron utilization regulators, Crp and Fur, in Escherichia coli. J Bacteriol 187(3):980-990
22. Zhong Z, Xu Z, Peng L, Huang L, Fang X, Cen P (2005) Tandem repeat mhBD2 gene enhance the soluble fusion expression of hBD2 in Escherichia coli. Appl Microbiol Biotechnol 1-7 (in press) DOI http://dx.doi.org/10.1007/s00253-005- 0212-6