References
- Sawabe, T., H. Takahashi, Y. Ezura, and P. Gacesa (2001) Cloning, sequence analysis and expression of Pseudoalteromonas elyakovii IAM 14594 gene (alyPEEC) encoding the extracellular alginate lyase. Carbohydr. Res. 335: 11-21 https://doi.org/10.1016/S0008-6215(01)00198-7
- Preiss, J. and G. Ashwell (1962) Alginic acid metabolism in bacteria. J. Biol. Chem. 237: 309-316
- Yoon, H. J., W. Hashimoto, O. Miyake, M. Okamoto, B. Mikami, and K. Murata (2000) Overexpression in Escherichia coli, purification, and characterization of Sphin-gomonas sp. Al alginate lyases. Protein Expr. Purif. 19: 84-90 https://doi.org/10.1006/prep.2000.1226
- Onsoyen, E. (1996) Commercial applications of alginates. Carbohydr. Eur. 14: 26-31
- Renn, D. (1997) Biotechnology and the red seaweed polysaccharide industry: status, needs and prospects. Trends Biotechnol. 15: 9-14 https://doi.org/10.1016/S0167-7799(96)10069-X
- Murata, K, T. Inose, T. Hisano, S. Abe, Y. Yonemoto, T. Yamashita, M. Takagi, K. Sakaguchi, A. Kimura, and T. Imanaka (1993) Bacterial alginate lyase: enzymology, genetics and application. J. Ferment. Bioeng. 76: 427-437 https://doi.org/10.1016/0922-338X(93)90040-F
- Kim, J. E., E. J. Kim, W. J. Rhee, and T. H. Park (2005) Enhanced production of recombinant protein in Escherichia coli using silkworm hemolymph. Biotechnol. Bioprocess Eng. 10:353-356 https://doi.org/10.1007/BF02931854
- Jin, H. H., N. S. Han, D. K. Kweon, Y. C. Park, and J. H. Seo (2001) Effects of environmental factors on in vivo folding of Bacillus macerans cyclodextrin glycosyltrans-ferase in recombinant Escherichia coli. J. Microbiol. Biotechnol. 11:92-96
- Kim, C. I., M. D. Kim, Y. C. Park, N. S. Han, and J. H. Seo (2000) Refolding of Bacillus macerans cyclodextrin glucanotransferase expressed as inclusion bodies in recombinant Escherichia coli. J. Microbiol. Biotechnol. 10: 632-637
- Kondo, A., J. Kohda, Y. Endo, T. Shiromizu, Y. Kurokawa, K. Nishihara, H. Yanagi, T. Yura, and H. Fukuda (2000) Improvement of productivity of active horseradish peroxidase in Escherichia coli by coexpression of Dsb proteins. J. Biosci. Bioeng. 90: 600-606 https://doi.org/10.1263/jbb.90.600
- Thomas, J. G., A. Ayling, and F. Baneyx (1997) Molecular chaperones, folding catalysts, and the recovery of active recombinant proteins from E. coli. Appl. Biochem. Biotechnol. 66: 197-238 https://doi.org/10.1007/BF02785589
- Kim, H. and I. H. Kim (2005) Refolding of fusion ferritin by gel filtration chromatography (GFC). Biotechnol. Bioprocess Eng. 10: 500-504 https://doi.org/10.1007/BF02932284
- Guan, Y.-X., H.-X. Pan, Y.-G. Gao, S.-J. Yao, and M.-G. Cho (2005) Refolding and purification of recombinant human interferon-y expressed as inclusion bodies in Escherichia coli using size exclusion chromatography. Biotechnol. Bioprocess Eng. 10: 122-127 https://doi.org/10.1007/BF02932581
- Kwon, M. J., S. L. Park, S. K. Kim, and S. W. Nam (2002) Overproduction of Bacillus macerans cyclodextrin glucanotransferase in E. coli by coexpression of GroEL/ES chaperone. J. Microbiol. Biotechnol. 12: 1002-1005
- Lamark, T., M. Ingebrigtsen, C. Bjornstad, T. Melkko, T. E. Mollnes, and E. W. Nielsen (2001) Expression of active human C1 inhibitor serpin domain in Escherichia coli. Protein Expr. Purif. 22: 349-358 https://doi.org/10.1006/prep.2001.1445
- Park, S. L., M. J. Kwon, S. K. Kim, and S. W. Nam (2004) GroEL/ES chaperone and low culture temperature synergistically enhanced the soluble expression of CGTase in E. coli. J. Microbiol. Biotechnol. 14: 216-219
- Sareen, D., R. Sharma, and R. M. Vohra (2001) Chaper-one-assisted overexpression of an active D-carbamoylase from Agrobacterium tumefaciens AM 10. Protein Expr. Purif. 23: 374-379 https://doi.org/10.1006/prep.2001.1532
- Hoshino, K., A. Eda, Y. Kurokawa, and N. Shimizu (2002) Production of brain-derived neurotrophic factor in Escherichia coli by coexpression of Dsb proteins. Biosci. Biotechnol. Biochem. 66: 344-350 https://doi.org/10.1271/bbb.66.344
- Kurokawa, Y., H. Yanagi, and T. Yura (2000) Overexpression of protein disulfide isomerase DsbD stabilize multiple-disulfide-bonded recombinant protein produced and transported to the periplasm in Escherichia coli. Appl. Environ. Microbiol. 66: 3960-3965 https://doi.org/10.1128/AEM.66.9.3960-3965.2000
- Han, M. J., S. J. Park, T. J. Park, and S. Y. Lee (2004) Roles and applications of small heat shock proteins in the production of recombinant proteins in Escherichia coli. Biotechnol. Bioeng. 88: 426-436 https://doi.org/10.1002/bit.20227
- Chung, K. T., T. H. Lee, and G. S. Kang (2003) Isolation of proteins that specifically interact with the ATPase domain of mammalian ER chaperone, BiP. Biotechnol. Bioprocess Eng. 8: 192-198 https://doi.org/10.1007/BF02935896
- Dumitru, G. L., Y. Groemping, D. Klostermeier, T. Restle, E. Deuerling, and J. Reinstein (2004) DafA cycles between the DnaK chaperone system and translationalmachinery. J. Mol.Biol. 339: 1179-1189 https://doi.org/10.1016/j.jmb.2004.04.052
- Diamant, S., A. P. Ben-Zvi, B. Bukau, and P. Goloubinoff (2000) Size-dependent disaggregation for stable protein aggregates by the DnaK chaperone machinery. J. Biol. Chem. 275:21107-21113 https://doi.org/10.1074/jbc.M001293200
- Gragerov, A., E. Nudler, N. Komissarova, G. A. Gaitanaris, M. E. Gottesman, and V. Nikiforov (1992) Cooperation of GroEL/GroES and DnaK/DnaJ heat shock proteins in preventing protein misfolding in Escherichia coli. Proc. Natl. Acad. Sci. USA 89: 10341-10344
- Szabo, A., T. Langer, H. Schroder, J. Flanagan, B. Bukau, and F. U. Hartl (1994) The ATP hydrolysis-dependent reaction cycle of the Escherichia coli Hsp70 system-DnaK, DnaJ, and GrpE. Proc. Natl. Acad. Sci. USA 91: 10345-. 10349
- Weissman, J. S., H. S. Rye, W. A. Fenton, J. M. Beechem, and A. L. Horwich (1996) Characterization of the active intermediate of a GroEL-GroES-mediated protein folding reaction. Cell 84: 481-490 https://doi.org/10.1016/S0092-8674(00)81293-3
- Ying, B. W., H. Taguchi, H. Ueda, and T. Ueda (2004) Chaperone-assisted folding of a single-chain antibody in a reconstituted translation system. Biochem. Biophys. Res. Commun. 320: 1359-1364 https://doi.org/10.1016/j.bbrc.2004.06.095
- Nishihara, K., M. Kanemori, M. Kitagawa, H. Yanagi, and T. Yura (1998) Chaperone coexpression plasmids: differential and synergistic roles of DnaK-DnaJ-GrpE and GroEL-GroES in assisting folding of an allergen of Japanese cedar pollen Cryj2, in Escherichia coli. Appl. Environ. Microbiol. 64: 1694-1699
- Yoon, H. J., Y. J. Choi, O. Miyake, W. Hashimoto, K. Murata, and B. Mikami (2001) Effect of Hisl92 mutation on the activity of alginate lyase A1 -III from Sphingomonas species A1. J. Microbiol. Biotechnol. 11: 118-123
- Hicks, S. J. and P. Gacesa (1996) Heterologous expression of full-length and truncated forms of the recombinant guluronate-specific alginate lyase of Klebsiella pneumoniae. Enzyme Microb. Technol. 19: 68-73 https://doi.org/10.1016/0141-0229(95)00175-1
- Gonzalez-Montalban, N., M. M. Carrio, S. Cuatrecasas, A. Aris, and A. Villaverde (2005) Bacterial inclusion bodies are cytotoxic in vivo in absence of functional chaperones DnaK or GroEL. J. Biotechnol. 118: 406-412 https://doi.org/10.1016/j.jbiotec.2005.05.024
- Park, S. L., E. J. Shin, S. P. Hong, S. J. Jeon, and S. W. Nam (2004) Production of soluble human granulocyte colony stimulating factor in E. coli by molecular chaperones. J. Microbiol. Biotechnol. 14: 216-219
- Chen, Y., J. Song, S. F. Sui, and D. N. Wang (2003) DnaK and DnaJ facilitated the folding process and reduced inclusion body formation of magnesium transporter CorA overexpressed in Escherichia coli. Protein Expr. Purif. 32:221-231 https://doi.org/10.1016/S1046-5928(03)00233-X
- Kwak, Y. H., S. J. Kim, K. Y Lee, and H. B. Kim (2000) Stress responses of the Escherichia coli groE promoter. J. Microbiol. Biotechnol. 10: 63-68