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Enzymes cofactor regeneration

For example, horse liver alcohol dehydrogenase (HLADH) was noncovalently immobihzed on a membrane and packed into a PBR [74] operated in a recirculated loop mode for the reduction of racemic 2-phenyl-tetrahydropyran-4-one 1 in the presence of NADH. The HLADH-reactor coupled with an enzymic cofactor regeneration system in the mobile phase could convert the substrate to the enantiopure (S,S)- and (R,S)-2. The immobilized HLADH reactor was stable over 6 months when stored at 5 °C. [Pg.204]

Because enzymes can be intraceUularly associated with cell membranes, whole microbial cells, viable or nonviable, can be used to exploit the activity of one or more types of enzyme and cofactor regeneration, eg, alcohol production from sugar with yeast cells. Viable cells may be further stabilized by entrapment in aqueous gel beads or attached to the surface of spherical particles. Otherwise cells are usually homogenized and cross-linked with glutaraldehyde [111-30-8] to form an insoluble yet penetrable matrix. This is the method upon which the principal industrial appHcations of immobilized enzymes is based. [Pg.291]

Coexpression of Genes for Carbonyl Reductase and Cofactor-Regenerating Enzymes... [Pg.203]

Figure 8.15 Coexpression of genes for carbonyl reductase and cofactor-regenerating enzymes [llc,dj. Figure 8.15 Coexpression of genes for carbonyl reductase and cofactor-regenerating enzymes [llc,dj.
In some cases it is more attractive to use whole microbial cells, rather than isolated enzymes, as biocatalysts. This is the case in many oxidative biotransformations where cofactor regeneration is required and/or the enzyme has low stability outside the cell. By performing the reaction as a fermentation, i.e. with growing microbial cells, the cofactor is continuously regenerated from the energy source, e.g. glucose. [Pg.50]

Kragl, 1J., Kruse, W., Hummel, W. and Wandrey, C. (1996) Enzyme engineering aspects of biocatalysis cofactor regeneration as example. Biotechnology and Bioengineering, 52, 309-319. [Pg.101]

Anaerobic bio-reduction of azo dye is a nonspecific and presumably extracellular process and comprises of three different mechanisms by researchers (Fig. 1), including the direct enzymatic reduction, indirect/mediated reduction, and chemical reduction. A direct enzymatic reaction or a mediated/indirect reaction is catalyzed by biologically regenerated enzyme cofactors or other electron carriers. Moreover, azo dye chemical reduction can result from purely chemical reactions with biogenic bulk reductants like sulfide. These azo dye reduction mechanisms have been shown to be greatly accelerated by the addition of many redox-mediating compounds, such as anthraquinone-sulfonate (AQS) and anthraquinone-disulfonate (AQDS) [13-15],... [Pg.88]

Cofactor regeneration is a necessary prerequisite for an in-vitro application of oxidoreductase enzymes, as the cofactors are too expensive to be used in stoichiometric amounts (Fig. 43.2) [17, 18]. [Pg.1471]

Scheme 43.2 Principal strategies of cofactor regeneration (En production enzyme E2 regeneration enzyme). Scheme 43.2 Principal strategies of cofactor regeneration (En production enzyme E2 regeneration enzyme).
Enzymatic cofactor regeneration can be subdivided into two categories the enzyme-coupled approach, where two different enzymes are used (one for the production reaction, and one for the regeneration reaction) and the substrate-coupled approach, where one and the same enzyme is used for both production and regeneration (E = E2). The most convenient and commonly used enzymatic regeneration systems are summarized in Table 43.1. [Pg.1474]

The use of redox enzymes in organic synthesis, while having a large potential for broad application in the selective formation of high-value compounds, has been limited by the necessity of cofactor regeneration or enzyme reactivation. Electrochemistry offers an attractive and, in principle, simple way to solve this problem because the mass-free electrons are used as regenerating agents. No... [Pg.91]

Therefore, for preparative applications of redox enzymes, effective and simple methods for the continuous recycling of the active cofactors have to be available. In addition, such systems must be stable over long time periods and the separation of the product must be simple to render technical processes economically feasible. Until now, this problem has generally been solved by the application of a second enzymatic reaction (enzyme-coupled regeneration, Fig. 2). [Pg.92]

Fig. 2, Principal of an enzyme-coupled cofactor regeneration system for an enzymatic reduction... Fig. 2, Principal of an enzyme-coupled cofactor regeneration system for an enzymatic reduction...
As most enzymes function under compatible ambient conditions, bio-bio cascades had already been successfully developed by the 1970s. By far, most examples have been reported in the field of carbohydrates, using combinations of enzymatic conversions (up to eight enzymes in one-pot), as well as for the in situ cofactor regeneration of enzymatic redox reactions towards amino and hydroxy acids. [Pg.277]

An impressive one-pot six-step enzymatic synthesis of riboflavine from glucose on the laboratory scale has been reported with an overall yield of 35-50%. Six different enzymes are involved in the various synthesis steps, while two other enzymes take care for the in situ cofactor regenerations [12]. This example again shows that many more multi-enzyme cascade conversions will be developed in the near future, as a much greater variety of enzymes in sufficient amounts for organic synthetic purposes will become available through rapid developments in genomics and proteomics. [Pg.280]

Unlike the whole-cell system, enzymatic reductions require the addition of a hydride donating cofactor to regenerate the reduced form of the enzyme. Depending on the chosen ADH, the cofactor is usually NADH or NADPH, both of which are prohibitively expensive for use in stoichiometric quantities at scale. Given the criticality of cofactor cost, numerous methods of in situ cofactor regeneration, both chemical and biocatalytic, have been investigated. However, only biocatalytic regeneration has so far proven to be sufficiently selective to provide the cofactor total turnover numbers of at least 10 required in production. [Pg.49]

Biocatalytic approaches to cofactor regeneration can be divided into coupled-enzyme methods and coupled-substrate methods.In the coupled-enzyme method, the oxidized cofactors (NAD+ and NADP+) are recycled in situ by performing an oxidation reaction using a second enzyme and an inexpensive auxiliary substrate. This second enzyme must employ the same cofactor, but neither enzyme should be able to accept the same substrate. [Pg.49]

In an extensive study, Okamoto and co-workers [76-86] introduced a biochemical switching device based on a cyclic enzyme system in which two enzymes share two cofactors in a cyclic manner. Cyclic enzyme systems have been used as biochemical amplitiers to improve the sensitivity of enzymatic analysis [87-89], and subsequently, this technique was introduced into biosensors [90-93], In addition, cyclic enzyme systems were also widely employed in enzymic reactors, in cases where cofactor regeneration is required [94-107], Using computer simulations, Okamoto and associates [77,80-83] investigated the characteristics of the cyclic enzyme system as a switching device, and their main model characteristics and simulation results are detailed in Table 1.1, as is a similar cyclic enzyme system introduced by Hjelmfelt et al. [109,116], which can be used as a logic element. [Pg.6]


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See also in sourсe #XX -- [ Pg.2 , Pg.456 ]

See also in sourсe #XX -- [ Pg.456 ]

See also in sourсe #XX -- [ Pg.456 ]

See also in sourсe #XX -- [ Pg.2 , Pg.456 ]

See also in sourсe #XX -- [ Pg.456 ]




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