Applications of the VHb Gene vgb for Improved Microbial Fermentation Processes

Methods in Enzymology

Volumn 436, Issue , 2008, Pages 273-287

  Wei, Xiao Xing ^a   Chen, Guo Qiang ^b  

^a TSINGHUA UNIVERSITY   (China)

^b SHANTOU UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GLOBIN; HEMOGLOBIN; OXYGEN; POLYHYDROXYALKANOIC ACID; ANTIINFECTIVE AGENT; BACTERIAL PROTEIN; HEMOGLOBIN PROTEIN, VITREOSCILLA; RECOMBINANT PROTEIN; TRUNCATED HEMOGLOBIN;

AEROBIC FERMENTATION; BIOREMEDIATION; CELL GROWTH; ENERGY METABOLISM; GLOBIN GENE; HOST; HYPOXIA; METABOLIC ENGINEERING; MICROBIAL RESPIRATION; NONHUMAN; OXYGEN TRANSPORT; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION; PROTEIN SYNTHESIS; REVIEW; VITREOSCILLA; ARTICLE; BACTERIAL GENE; BIOSYNTHESIS; BIOTECHNOLOGY; ESCHERICHIA COLI; FERMENTATION; GENETICS; METABOLISM;

VITREOSCILLA;

ANTI-BACTERIAL AGENTS; BACTERIAL PROTEINS; BIODEGRADATION, ENVIRONMENTAL; BIOTECHNOLOGY; ESCHERICHIA COLI; FERMENTATION; GENES, BACTERIAL; OXYGEN; POLYHYDROXYALKANOATES; PROMOTER REGIONS (GENETICS); RECOMBINANT PROTEINS; TRUNCATED HEMOGLOBINS; VITREOSCILLA;

EID: 42949144463     PISSN: 00766879     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0076-6879(08)36015-7     Document Type: Chapter

References (62)

1. Allocatelli C.T., Cutruzzola F., Brancaccio A., Vallone B., and Brunori M. Engineering Ascaris hemoglobin oxygen-affinity in sperm whale myoglobin: Role of tyrosine B10. FEBS Lett. 352 (1994) 63-66
2. Aydin S., Webster D.A., and Stark B.C. Nitrite inhibition of Vitreoscilla hemoglobin (VHb) in recombinant E. coli: Direct evidence that VHb enhances recombinant protein production. Biotechnol. Prog. 16 (2000) 917-921
3. Bailey J.E. Chemical engineering of cellular processes. Chemical Engineering Science 50 (1995) 4091-4108
4. Bhave S.L., and Chattoo B.B. Expression of Vitreoscilla hemoglobin improves growth and levels of extracellular enzyme in Yarrowia lipolytica. Biotech. Bioeng. 84 (2003) 658-666
5. Bogusz D., Appleby C.A., Landsmann J., Dennis E.S., Trinick M.J., and Peacock W.J. Functioning haemoglobin genes in non-nodulating plants. Nature 331 (1988) 178-180
6. Brunker P., Minas W., Kallio P.T., and Bailey J.E. Genetic engineering of an industrial strain of Saccharopolyspora erythraea for stable expression of the Vitreoscilla haemoglobin gene (vhb). Microbiology-UK 144 (1998) 2441-2448
7. Bulow L., Holmberg N., Lilius G., and Bailey J.E. The metabolic effects of native and transgenic hemoglobins on plants. Trends Biotechnol. 17 (1999) 21-24
8. Chen W., Hughes D.E., and Bailey J.E. Intracellular expression of Vitreoscilla hemoglobin alters the aerobic metabolism of Saccharomyces cerevisiae. Biotechnol. Prog. 10 (1994) 308-313
9. Chien L.J., Chen H.T., Yang P.F., and Lee C.K. Enhancement of cellulose pellicle production by constitutively expressing Vitreoscilla hemoglobin in Acetobacter xylinum. Biotechnol. Prog. 22 (2006) 1598-1603
10. Chung J.W., Webster D.A., Pagilla K.R., and Stark B.C. Chromosomal integration of the Vitreoscilla hemoglobin gene in Burkholderia and Pseudomonas for the purpose of producing stable engineered strains with enhanced bioremediating ability. J. Ind. Microbiol. Biotechnol. 27 (2001) 27-33
11. Dikshit K.L., and Webster D.A. Cloning, characterization and expression of the bacterial globin gene from Vitreoscilla in Escherichia coli. Gene 70 (1988) 377-386
12. Dogan I., Pagilla K.R., Webster D.A., and Stark B.C. Expression of Vitreoscilla hemoglobin in Gordonia amarae enhances biosurfactant production. J. Ind. Microbiol. Biotechnol. 33 (2006) 693-700
13. Erenler S.O., Gencer S., Geckil H., Stark B.C., and Webster D.A. Cloning and expression of the Vitreoscilla hemoglobin gene in Enterobacter aerogenes: Effect on cell growth and oxygen uptake. Applied Biochemistry and Microbiology 40 (2004) 241-248
14. Farres J., and Kallio P.T. Improved cell growth in tobacco suspension cultures expressing Vitreoscilla hemoglobin. Biotechnol. Prog. 18 (2002) 229-233
15. Favey S., Labesse G., Vouille V., and Boccara M. Flavohaemoglobin Hmpx: A new pathogenicity determinant in Erwinia chrysanthemi strain-3937. Microbiology-UK 141 (1995) 863-871
16. Frey A.D., Farres J., Bollinger C.J.T., and Kallio P.T. Bacterial hemoglobins and flavohemoglobins for alleviation of nitrosative stress in Escherichia coli. Appl. Environ. Microbiol. 68 (2002) 4835-4840
17. Geckil H., Arman A., Gencer S., Ates B., and Yilmaz H.R. Vitreoscilla hemoglobin renders Enterobacter aerogenes highly susceptible to heavy metals. Biometals 17 (2004) 715-723
18. Geckil H., Barak Z., Chipman D.M., Erenler S.O., Webster D.A., and Stark B.C. Enhanced production of acetoin and butanediol in recombinant Enterobacter aerogenes carrying Vitreoscilla hemoglobin gene. Bioprocess Biosyst. Eng. 26 (2004) 325-330
19. Geckil H., Gencer S., Ates B., Ozer U., Uckun M., and Yilmaz I. Effect of Vitreoscilla hemoglobin on production of a chemotherapeutic enzyme, L-asparaginase, by Pseudomonas aeruginosa. Biotechnol. J. 1 (2006) 203-208
20. Gibson Q.H., and Smith M.H. Rates of reaction of Ascaris haemoglobins with ligands. Proc. R. Soc. Lond. B Biol. Sci. 163 (1965) 206-214
21. Gibson Q.H., Wittenberg J.B., Wittenberg B.A., Bogusz D., and Appleby C.A. The kinetics of ligand binding to plant hemoglobins: Structural implications. J. Biol. Chem. 264 (1989) 100-107
22. Holmberg N., Lilius G., Bailey J.E., and Bulow L. Transgenic tobacco expressing Vitreoscilla hemoglobin exhibits enhanced growth and altered metabolite production. Nature Biotechnol. 15 (1997) 244-247
23. Ingledew W.J., and Poole R.K. The respiratory chains of Escherichia coli. Microbiol. Rev. 48 (1984) 222-271
24. Kallio P.T., and Bailey J.E. Intracellular expression of Vitreoscilla hemoglobin (VHb) enhances total protein secretion and improves the production of alpha-amylase and neutral protease in Bacillus subtilis. Biotechnol. Prog. 12 (1996) 31-39
25. Kallio P.T., Kim D.J., Tsai P.S., and Bailey J.E. Intracellular expression of Vitreoscilla hemoglobin alters Escherichia coli energy-metabolism under oxygen-limited conditions. Eur. J. Biochem. 219 (1994) 201-208
26. Kang D.G., Kim Y.K., and Cha H.J. Comparison of green fluorescent protein expression in two industrial Escherichia coli strains, BL21 and W3110, under co-expression of bacterial hemoglobin. Appl. Microbiol. Biotechnol. 59 (2002) 523-528
27. Khleifat K.M. Correlation between bacterial hemoglobin and carbon sources: Their effect on copper uptake by transformed E. coli strain alpha DH5. Curr. Microbiol. 52 (2006) 64-68
28. Khosla C., and Bailey J.E. Heterologous expression of a bacterial haemoglobin improves the growth properties of recombinant Escherichia coli. Nature 331 (1988) 633-635
29. Khosla C., and Bailey J.E. The Vitreoscilla hemoglobin gene: Molecular cloning, nucleotide sequence and genetic expression in Escherichia coli. Mol. Gen. Genet. 214 (1988) 158-161
30. Khosla C., and Bailey J.E. Characterization of the oxygen-dependent promoter of the Vitreoscilla hemoglobin gene in Escherichia coli. J. Bacteriol. 171 (1989) 5995-6004
31. Khosla C., Curtis J.E., DeModena J., Rinas U., and Bailey J.E. Expression of intracellular hemoglobin improves protein synthesis in oxygen-limited Escherichia coli. Biotechnology (NY) 8 (1990) 849-853
32. Khosravi M., Webster D.A., and Stark B.C. Presence of the bacterial hemoglobin gene improves alpha-amylase production of a recombinant Escherichia coli strain. Plasmid 24 (1990) 190-194
33. Konz J.O., King J., and Cooney C.L. Effects of oxygen on recombinant protein expression. Biotechnol. Prog. 14 (1998) 393-409
34. Lin J.M., Stark B.C., and Webster D.A. Effects of Vitreoscilla hemoglobin on the 2,4-dinitrotoluene (2,4-DNT) dioxygenase activity of Burkholderia and on 2,4-DNT degradation in two-phase bioreactors. J. Ind. Microbiol. Biotechnol. 30 (2003) 362-368
35. Liu T., Chen J.Y., Zheng Z., Wang T.H., and Chen G.Q. Construction of highly efficient E. coli expression systems containing low oxygen induced promoter and partition region. Appl. Microbiol. Biotechnol. 68 (2005) 346-354
36. Minas W., Brunker P., Kallio P.T., and Bailey J.E. Improved erythromycin production in a genetically engineered industrial strain of Saccharopolyspora erythraea. Biotechnol. Prog. 14 (1998) 561-566
37. Orii Y., and Webster D.A. Photodissociation of oxygenated cytochrome o(s) (Vitreoscilla) and kinetic studies of reassociation. J. Biol. Chem. 261 (1986) 3544-3547
38. Ouyang S.P., Han J., Qiu Y.Z., Qin L.F., Chen S., Wu Q., Leski M.L., and Chen G.Q. Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) production in recombinant Aeromonas hydrophila 4AK4 harboring phbA, phbB and vgb genes. Macromolecular Symposia 224 (2005) 21-34
39. Patel S.M., Stark B.C., Hwang K.W., Dikshit K.L., and Webster D.A. Cloning and expression of Vitreoscilla hemoglobin gene in Burkholderia sp strain DNT for enhancement of 2,4-dinitrotoluene degradation. Biotechnol. Prog. 16 (2000) 26-30
40. Pendse G.J., and Bailey J.E. Effect of Vitreoscilla hemoglobin expression on growth and specific tissue: Plasminogen activator productivity in recombinant Chinese-hamster ovary cells. Biotechnol. Bioengin. 44 (1994) 1367-1370
41. Schubert P., Steinbuchel A., and Schlegel H.G. Cloning of the Alcaligenes eutrophus genes for synthesis of poly-beta-hydroxybutyric acid (PHB) and synthesis of PHB in Escherichia coli. J. Bacteriol. 170 (1988) 5837-5847
42. So J.H., Webster D.A., Stark B.C., and Pagilla K.R. Enhancement of 2,4-dinitrotoluene biodegradation by Burkholderia sp. in sand bioreactors using bacterial hemoglobin technology. Biodegradation 15 (2004) 161-171
43. Springer B.A., Egeberg K.D., Sligar S.G., Rohlfs R.J., Mathews A.J., and Olson J.S. Discrimination between oxygen and carbon monoxide and inhibition of autooxidation by myoglobin: Site-directed mutagenesis of the distal histidine. J. Biol. Chem. 264 (1989) 3057-3060
44. Suen W.C., and Spain J.C. Cloning and characterization of Pseudomonas sp. strain DNT genes for 2,4-dinitrotoluene degradation. J. Bacteriol. 175 (1993) 1831-1837
45. Suthar D.H., and Chattoo B.B. Expression of Vitreoscilla hemoglobin enhances growth and levels of alpha-amylase in Schwanniomyces occidentalis. Appl. Microbiol. Biotechnol. 72 (2006) 94-102
46. Tabakov V.Y., Emelyanova L.K., Antonova S.V., and Voeikova A. Effect of the bacterial hemoglobin vhb gene on the efficiency of intergeneric conjugation in Escherichia coli: Streptomyces and biosynthesis of antibiotics in Streptomyces. Russian Journal of Genetics 37 (2001) 332-334
47. Tarricone C., Calogero S., Galizzi A., Coda A., Ascenzi P., and Bolognesi M. Expression, purification, crystallization, and preliminary X-ray diffraction analysis of the homodimeric bacterial hemoglobin from Vitreoscilla stercoraria. Proteins 27 (1997) 154-156
48. Unden G., and Schirawski J. The oxygen-responsive transcriptional regulator FNR of Escherichia coli: The search for signals and reactions. Mol. Microbiol. 25 (1997) 205-210
49. Urgun-Demirtas M., Stark B., and Pagilla K. Use of genetically engineered microorganisms (GEMs) for the bioremediation of contaminants. Crit. Rev. Biotechnol. 26 (2006) 145-164
50. Urlacher V.B., Lutz-Wahl S., and Schmid R.D. Microbial P450 enzymes in biotechnology. Appl. Microbiol. Biotechnol. 64 (2004) 317-325
51. Wakabayashi S., Matsubara H., and Webster D.A. Primary sequence of a dimeric bacterial haemoglobin from Vitreoscilla. Nature 322 (1986) 481-483
52. Webster D.A. Structure and function of bacterial hemoglobin and related proteins. Adv. Inorg. Biochem. 7 (1988) 245-265
53. Webster D.A., and Hackett D.P. The purification and properties of cytochrome o from Vitreoscilla. J. Biol. Chem. 241 (1966) 3308-3315
54. Webster D.A., and Liu C.Y. Reduced nicotinamide adenine dinucleotide cytochrome o reductase associated with cytochrome o purified from Vitreoscilla: Evidence for an intermediate oxygenated form of cytochrome o. J. Biol. Chem. 249 (1974) 4257-4260
55. Wei M.L., Webster D.A., and Stark B.C. Genetic engineering of Serratia marcescens with bacterial hemoglobin gene: Effects on growth, oxygen utilization, and cell size. Biotechnol. Bioengin. 57 (1998) 477-483
56. Wen Y., Song Y., and Li J.L. [The effects of Vitreoscilla hemoglobin expression on growth and antibiotic production in Streptomyces cinnamonensis]. Sheng Wu Gong Cheng Xue Bao 17 (2001) 24-28
57. Wu J.M., Hsu T.A., and Lee C.K. Expression of the gene coding for bacterial hemoglobin improves beta-galactosidase production in a recombinant Pichia pastoris. Biotechnol. Lett. 25 (2003) 1457-1462
58. Yang J., Webster D.A., and Stark B.C. ArcA works with Fnr as a positive regulator of Vitreoscilla (bacterial) hemoglobin gene expression in Escherichia coli. Microbiol. Res. 160 (2005) 405-415
59. Yang Y.G., Zhang H.T., Tong Q., Yang Y.H., Wang Y., Yang S.L., and Gong Y. Construction of a novel engineering strain E-coli G830, which is adoptable to high-cell-density fermentation. Acta Biochim. Biophys. 33 (2001) 296-302
60. Yu H.M., Shi Y., Zhang Y.P., Yang S.L., and Shen Z.Y. Effect of Vitreoscilla hemoglobin biosynthesis in Escherichia coli on production of poly(beta-hydroxybutyrate) and fermentative parameters. FEMS Microbiol. Lett. 214 (2002) 223-227
61. Zhang L., Li Y., Wang Z., Xia Y., Chen W., and Tang K. Recent developments and future prospects of Vitreoscilla hemoglobin application in metabolic engineering. Biotechnol. Adv. 25 (2007) 123-136
62. Zhu H., Wang T.W., Sun S.J., Shen Y.L., and Wei D.Z. Chromosomal integration of the Vitreoscilla hemoglobin gene and its physiological actions in Tremella fuciformis. Appl. Microbiol. Biotechnol. 72 (2006) 770-776