Immobilized multi

Thermal biosensors have attracted less consideration. Moreover, adverse comments like complicated thermostating, very weak sensitivity or non-specific heating effects have resulted in a poor reputation. Actually, this trend is surprising because thermal biosensors have influenced the whole of biosensor research over and over again (Mosbach, 1991). Especially the enzyme thermistor (ET) has enriched our knowledge about immobilized multi-enzyme systems for signal amplification, the use of immobilized coenzymes and different immobilization techniques. Moreover, ET basic research was decisive for immunosenso-rics or concanavalin-A-based reversible biosensors. Thermal biosensors have multiple advantages ... 

Murakami Y, Takeuchi T, Yokoyama K, Tamiya E, Karube I and Suda M 1993 Integration of enzyme-immobilized column with electrochemical flow cell using micromachining techniques for a glucose detection system Anal. Chem. 65 2731-5 Olson B, Stalbom B and Johansson G 1986 Determination of sucrose in the presence of glucose in a flow Injection system with immobilized multi-enzyme reactors Anal. Chim. Acta 179 203-8... 

B. Olsson, B. Stalbom, and G. Johansson, Determination of Sucrose in the Presence of Glucose in a Flow-Injection System with Immobilized Multi-Enzyme Reactors. Anal. Chim. Acta, 179 (1986) 203. 

Immobilization. Enzymes, as individual water-soluble molecules, are generally efficient catalysts. In biological systems they are predorninandy intracellular or associated with cell membranes, ie, in a type of immobilized state. This enables them to perform their activity in a specific environment, be stored and protected in stable form, take part in multi-enzyme reactions, acquire cofactors, etc. Unfortunately, this optimization of enzyme use and performance in nature may not be directiy transferable to the laboratory. 

Another approach, developed in our laboratory, consists of the compartmentalization of the sensing layer25"27. This concept, only applicable for multi-enzyme based sensors, consist in immobilizing the luminescence enzymes and the auxiliary enzymes on different membranes and then in stacking these membranes at the sensing tip of the optical fibre sensor. This configuration results in an enhancement of the sensor response, compared with the case where all the enzymes are co-immobilized on the same membrane. This was due to an hyperconcentration of the common intermediate, i.e. the final product of the auxiliary enzymatic system, which is also the substrate of the luminescence reaction, in the microcompartment existing between the two stacked membranes. 

Poly(dimethylsiloxane) (PDMS) as an immobilization matrix has been successfully used to design multi-purpose biochips i.e., for either nucleic... 

A.L. Crumbliss, J.Z. Stonehuerner, R.W. Henkens, J. Zhao, and J.P. O Daly, A carrageenan hydrogel stabilized colloidal gold multi-enzyme biosensor electrode utilizing immobilized horseradish peroxidase and cholesterol oxidase/cholesterol esterase to detect cholesterol in serum and whole blood. Biosens. Bioelectron. 8, 331-337 (1993). 

EIA systems take advantage of the extreme specificity and affinity with which antibodies bind antigens which stimulated their initial production, coupled to the catalytic efficiency of enzymes, which facilitates signal amplification as well as straightforward detection and quantification. In most such systems, the antibody is immobilized on the internal walls of the wells in a multi-well microtitre plate, which therefore serves as collection of reaction mini-test tubes. 

Storer RI, Takemoto T, Jackson PS, Brown DS, Baxendale IR, Ley SV (2004) Multi-step application of immobilized reagents and scavengers a total synthesis of epothilone C. Chem Eur J 10 2529-2547... 

Once an enzyme-catalysed reaction has occurred the product is released and its engagement with the next enzyme in the sequence is a somewhat random event. Only rarely is the product from one reaction passed directly onto the next enzyme in the sequence. In such cases, enzymes which catalyse consecutive reactions, are physically associated or aggregated with each other to form what is called a multi enzyme complex (MEC). An example of this arrangement is evident in the biosynthesis of saturated fatty acids (described in Section 6.30). Another example of an organized arrangement is one in which the individual enzyme proteins are bound to membrane, as for example with the ATP-generating mitochondrial electron transfer chain (ETC) mechanism. Intermediate substrates (or electrons in the case of the ETC) are passed directly from one immobilized protein to the next in sequence. 

The one-pot dynamic kinetic resolution (DKR) of ( )-l-phenylethanol lipase esterification in the presence of zeolite beta followed by saponification leads to (R)-l phenylethanol in 70 % isolated yield at a multi-gram scale. The DKR consists of two parallel reactions kinetic resolution by transesterification with an immobilized biocatalyst (lipase B from Candida antarctica) and in situ racemization over a zeolite beta (Si/Al = 150). With vinyl octanoate as the acyl donor, the desired ester of (R)-l-phenylethanol was obtained with a yield of 80 % and an ee of 98 %. The chiral secondary alcohol can be regenerated from the ester without loss of optical purity. The advantages of this method are that it uses a single liquid phase and both catalysts are solids which can be easily removed by filtration. This makes the method suitable for scale-up. The examples given here describe the multi-gram synthesis of (R)-l-phenylethyl octanoate and the hydrolysis of the ester to obtain pure (R)-l-phenylethanol. 

The use of SCCO2 either alone [135-137] or in multi-phase systems [138-140] offers interesting process alternatives to other methods of catalyst immobilization such as heterogenization on solid supports [126-128], aqueous... 

Kaldor [49 i, 55] demonstrated the advantages of applying solid-supported scavengers to the preparation of parallel arrays in a multi-step fashion. In these studies he examined the clean-up of multiple amine alkylation and acylation reactions using a variety of immobilized electrophilic and nucleophilic scavenger reagents including an amine, isocyanate, aldehyde and acid chloride (Tab. 2.1). 

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