Application of affinity adsorption in thienamycin fermentation
dc.contributor.author | Wang, Henry Y. | en_US |
dc.contributor.author | Palanki, Srinivas | en_US |
dc.contributor.author | Hyatt, Gregory S. | en_US |
dc.date.accessioned | 2006-09-11T18:10:10Z | |
dc.date.available | 2006-09-11T18:10:10Z | |
dc.date.issued | 1989-02 | en_US |
dc.identifier.citation | Wang, Henry Y.; Palanki, Srinivas; Hyatt, Gregory S.; (1989). "Application of affinity adsorption in thienamycin fermentation." Applied Microbiology and Biotechnology 30(2): 115-119. <http://hdl.handle.net/2027.42/46759> | en_US |
dc.identifier.issn | 0175-7598 | en_US |
dc.identifier.issn | 1432-0614 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/46759 | |
dc.description.abstract | Many antibiotic fermentations are sensitive to high concentrations of their own product possibly due to product regulation and toxicity mechanisms. In this paper we discuss the feasibility of using affinity adsorption with biospecific ligands for in situ product removal to alleviate this problem. The concept of using whole cells containing the biospecific ligands is demonstrated in the case of thienamycin fermentation using whole cells of Bacillus stearothermophilus and immobilized β-lactamase. It is observed that thienamycin production continues for an extended period of time. | en_US |
dc.format.extent | 446046 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Springer-Verlag | en_US |
dc.subject.other | Chemistry | en_US |
dc.subject.other | Microbiology | en_US |
dc.subject.other | Biotechnology | en_US |
dc.subject.other | Microbial Genetics and Genomics | en_US |
dc.title | Application of affinity adsorption in thienamycin fermentation | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Chemical Engineering, The University of Michigan, 48109, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationum | Department of Chemical Engineering, The University of Michigan, 48109, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationum | Department of Chemical Engineering, The University of Michigan, 48109, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/46759/1/253_2004_Article_BF00263996.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1007/BF00263996 | en_US |
dc.identifier.source | Applied Microbiology and Biotechnology | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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