Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/392
DC FieldValueLanguage
dc.contributor.authorĐorđević, Markoen_US
dc.contributor.authorDjordjevic, Magdalenaen_US
dc.date.accessioned2019-07-01T20:29:49Z-
dc.date.available2019-07-01T20:29:49Z-
dc.date.issued2012-10-01-
dc.identifier.issn1478-3967-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/392-
dc.description.abstractA recently emerging discipline of synthetic biology has the aim of constructing new biosynthetic pathways with useful biological functions. A major application of these pathways is generating a large amount of the desired product. However, toxicity due to the possible presence of toxic precursors is one of the main problems for such production. We consider here the problem of generating a large amount of product from a potentially toxic substrate. To address this, we propose a simple biosynthetic pathway, which can be induced in order to produce a large number of the product molecules, by keeping the substrate amount at low levels. Surprisingly, we show that the large product generation crucially depends on fast non-specific degradation of the substrate molecules. We derive an optimal induction strategy, which allows as much as three orders of magnitude increase in the product amount through biologically realistic parameter values. We point to a recently discovered bacterial immune system (CRISPR/Cas in E. coli) as a putative example of the pathway analysed here. We also argue that the scheme proposed here can be used not only as a stand-alone pathway, but also as a strategy to produce a large amount of the desired molecules with small perturbations of endogenous biosynthetic pathways. © 2012 IOP Publishing Ltd.en_US
dc.language.isoenen_US
dc.relation.ispartofPhysical Biologyen_US
dc.titleA simple biosynthetic pathway for large product generation from small substrate amountsen_US
dc.typeArticleen_US
dc.identifier.doi10.1088/1478-3975/9/5/056004-
dc.identifier.pmid22931893-
dc.identifier.scopus2-s2.0-84866340877-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84866340877-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0002-2903-3119-
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