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Plant and animal cells

D-ribose, CjHioOj. M.p. 87 0. The sugar of ribonucleic acid it is therefore present in all plant and animal cells. It has the furanose structure shown. [Pg.346]

Plant and animal cells have numerous chromosomes. Growth rates are relatively slow. A typical nutrient medium will contain a large number of vitamins and growth factors in addition to complex nitrogen sources, because other specialized cells in the original structures supply these needs. A plant or animal cell is not hke a microbial cell in its ability to function independently. [Pg.2132]

All K channels are tetrameric molecules. There are two closely related varieties of subunits for K channels, those containing two membrane-spanning helices and those containing six. However, residues that build up the ion channel. Including the pore helix and the inner helix, show a strong sequence similarity among all K+ channels. Consequently, the structural features and the mechanism for ion selectivity and conductance described for the bacterial K+ channel in all probability also apply for K+ channels in plant and animal cells. [Pg.234]

Microbial cells, rather than plant and animal cells, are generally preferred for the production of organic chemicals. There are several reasons for this. [Pg.13]

Although it is possible to obtain cells from whole animals or plants and to cultivate them in suitable nutrient solutions, in general they are not as easy to handle as microbes. Nevertheless, plant and animal cells are a valuable genetic resource for biotechnology and many newly developed bioprocesses rely on transfer of their genes to micro-organisms. [Pg.14]

In low shear, there is low mixing which means the bioreactor can be used for growing plant and animal cells. [Pg.145]

Why Do We Need to Know This Material Chapter 9 developed the concepts of chemical equilibria in gaseous systems this chapter extends those ideas to aqueous systems, which are important throughout chemistry and biology. Equilibria between acids, bases, and water in plant and animal cells are vital for the survival of individual organisms. To sustain human societies and protect our ecosystems, we also need these ideas to understand the acidity of rain, natural waters such as lakes and rivers, and municipal water supplies. [Pg.515]

Three major intellectual frontiers for chemical engineers in bioprocessing are the design of bioreactors for the culture of plant and animal cells, the development of control systems along with the needed biosensors and analytical instraments, and the development of processes for separating and purifying products. A critical component in each of these three research areas is the need to relate the micro-scale to the mesoscale. [Pg.41]

One problem mentioned earlier is that certain animal cells are anchorage-dependent. Also, plant and animal cells are easily raptured by mechanical shear. Bioreactors for handhng such cells must be designed so that the contents of the reactor can be mixed without disrupting the cells. A similar problem exists in the design of systems to transfer the cells from one vessel to another. [Pg.41]

Special reactors are required to conduct biochemical reactions for the transformation and production of chemical and biological substances involving the use of biocatalysts (enzymes, immobilised enzymes, microorganisms, plant and animal cells). These bioreactors have to be designed so that the enzymes or living organisms can be used under defined, optimal conditions. The bioreactors which are mainly used on laboratory scale and industrially are roller bottles, shake flasks, stirred tanks and bubble columns (see Table 1). [Pg.41]

Jervis L, Robertson ER (1987) In Webb C, Mavituna E (eds) Plant and animal cells process possibilities. Ellis Horwood, Chichester, p 216... [Pg.175]

Large-scale plant and animal cell culture... [Pg.337]

Some non-silica sol-gel materials have also been developed to immobilize bioactive molecules for the construction of biosensors and to synthesize new catalysts for the functional devices. Liu et al. [33] proved that alumina sol-gel was a suitable matrix to improve the immobilization of tyrosinase for detection of trace phenols. Titania is another kind of non-silica material easily obtained from the sol-gel process [34, 35], Luckarift et al. [36] introduced a new method for enzyme immobilization in a bio-mimetic silica support. In this biosilicification process precipitation was catalyzed by the R5 peptide, the repeat unit of the silaffin, which was identified from the diatom Cylindrotheca fusiformis. During the enzyme immobilization in biosilicification the reaction mixture consisted of silicic acid (hydrolyzed tetramethyl orthosilicate) and R5 peptide and enzyme. In the process of precipitation the reaction enzyme was entrapped and nm-sized biosilica-immobilized spheres were formed. Carturan et al. [11] developed a biosil method for the encapsulation of plant and animal cells. [Pg.530]

Relatively less work has been done on immobilization of plant and animal cells and spores of microbes in silica matrixes. The main drawback is less viability of the cells in sol-gel matrices. Thus more refined methods are required to utilize harness of the whole cells entrapped in sol-gel matrices and biosensing applications. At the same time studies such as interactions between sol-gel matrices and whole cells and metabolic changes during immobilization have to be closely monitored for the exploration of new matrices and methods. [Pg.546]

Fig. 2.2 Stability of IgCi monoclonal antibody added to sterile plant and animal cell culture media. ( ) Murashige and Skoog (MS) medium (A) Dulbecco s minimal essential medium (DMEM) with 10% serum and (A) serum-free Ex-cell 302 medium. The error bars indicate standard errors from triplicate flasks. (Reproduced with permission, from B. M. -Y. Tsoi and P. M. Doran, Biotechnol. Appi. Bio-chem. 2002, 35, 171-180. Portland Press on behalf of the IUBMB.)... Fig. 2.2 Stability of IgCi monoclonal antibody added to sterile plant and animal cell culture media. ( ) Murashige and Skoog (MS) medium (A) Dulbecco s minimal essential medium (DMEM) with 10% serum and (A) serum-free Ex-cell 302 medium. The error bars indicate standard errors from triplicate flasks. (Reproduced with permission, from B. M. -Y. Tsoi and P. M. Doran, Biotechnol. Appi. Bio-chem. 2002, 35, 171-180. Portland Press on behalf of the IUBMB.)...
Hexokinase is of great biological interest since it would appear that not only in yeast cells but in most, if not all, plant and animal cells phosphorylation at C6 of the common hexoses D-glucose, D-fructose and D-mannose initiates sugar utilization. Since on solution in water the crystalline hexoses quickly undergo mutarotation, resulting in an equilibrium mixture of various tautomeric modifications, the fermentability... [Pg.86]

Wohler. Synthesis of urea from ammonium cyanate. Microscopic examination of plant and animal cells by Dutrochet, Schlieden, and Schwann led to acceptance of the cellular origin of all tissues. ... [Pg.191]


See other pages where Plant and animal cells is mentioned: [Pg.473]    [Pg.2057]    [Pg.2129]    [Pg.2131]    [Pg.2132]    [Pg.2142]    [Pg.232]    [Pg.830]    [Pg.11]    [Pg.13]    [Pg.385]    [Pg.41]    [Pg.99]    [Pg.197]    [Pg.33]    [Pg.75]    [Pg.289]    [Pg.295]    [Pg.84]    [Pg.526]    [Pg.545]    [Pg.545]    [Pg.272]    [Pg.87]    [Pg.179]    [Pg.61]    [Pg.51]    [Pg.33]    [Pg.231]    [Pg.428]   


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Animal and Plant Cell Cultures

Cells and Animals

Cells, animal plant

Plant and animal whole cells, in sol-gel matrices

Plant cell

Plants and animals

Sol-gel matrices plant and animal cells

Whole-cell encapsulation, in sol-gels plant and animal cells

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