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Free Cells

The cells primarily engaged in phagocytosis are the freely movable macrophages (true wandering cells) and reticulum cells (fixed macrophages, resting [Pg.421]

Mast cells with their metachromatic granules (0.3 to 1.0 [xm in diameter) as their hallmarks produce histamine, which has marked vasoactive effects and also seems to enhance oxygen radical formation by phagocytes (Friedl et al. 1989). [Pg.421]

As the injection of CaCh (0.1 M) into individual rat peritoneal mast cells elicited secretory granule extrusion (Kanno et al. 1973), calcium might be involved in some stage of the secretion process (Goth 1978). M-benzhydryl-hT-p-hydroxybenzyl-piperazine, a potent anti-histaminic and anti-sero-toninergic calcium blocker, prevented mast cells from degranulation (Fig. 195), while the introduction of particulate matter into the body induced mast cell degranulation (Fig. 196). [Pg.421]


Identify which of the following statements are true for immobilised biocatalysts, when compared to free enzyme or free cell systems. [Pg.17]

Process B Genetic instability Poor enzyme stability Cofactor requirement Product (non-polar) inhibition Biocatalyst Free enzyme Free cells Immobilised enzyme Immobilised cells... [Pg.33]

It would seem that immobilisation looks very promising, but remember that the costs of immobilisation and the addition of cofactor have to be compared with the cost of production by free cells. [Pg.268]

Cell immobilisation is costly in comparison to the production of free cells. [Pg.268]

True Hie concentration of immobilised biocatalyst in a reactor can be much greater than for systems using soluble of free cells. [Pg.341]

The economics of an immobilised cell process depend on the lifetime of the microorganism and a continued level of clean product delivered by the fixed cells. It is important to eliminate the free cells from the downstream product without the use of any units such as centrifuge or filtration processes. Since the cells are retained in the ICR, the activity of intracellular enzymes may play a major role. It is assumed that the deactivation of the enzyme at constant temperature follows a first-order equation as shown below 17... [Pg.218]

Significant differences are also apparent for the effect of pH on the fermentation rate. The narrow pH optimum characteristic of a free cell system is replaced by an extremely broad range upon immobilisation. This effect stems from the gradient pH that exists within the bead. [Pg.227]

Substrates other than free cells were also examined for luminescence activity in the presence of tin and flavonol. For example, glass slides covered with a well-developed but uncharacterized biofllm growth were exposed to 4.5 x 10 H n-butyltin trichloride in ethanol for 60 min. The slides were subsequently rinsed with ethanol and exposed to 1.4 x H... [Pg.88]

Another attribute of CA dynamics is the average size of clusters of cells. This is certainly influenced by the choice of J and Pb rules and should parallel some physical properties. Other attributes that can be measured and used to link with physical properties include the average number of joined faces of a molecule and the number of free cell faces. Each of these attributes has been exploited for their ability to relate to the physical properties. The choice of J and Pb rules, therefore, must be made with some attention to their attributes produced and their ability to mirror physical properties as a function of systematic rule changes. [Pg.46]

Xylose-rich pectic polysaccharide was extracted from defatted and protein-free cell wall preparation (5) using HCl solution (pH 1.6) at 85° C for 4 h. The extract was adjusted to pH 5.0 with ammonia, concentrated on a rotary evaporator under reduced pressure at 40°C, and precipitated with 5 volumes of 96% ethanol. After washing twice with 80% ethanol and drying in an air circulated oven at 40°C for 2 h, the pellet was ledissolved with distilled water and then precipitated with 4 vols 96% ethanol. Before the pellet was gently ground, the precipitated pellet was washed twice with 70% ethanol and dried at 40 ° in an air circulated oven for 16 h. The resultant white powder was labelled "xylose-rich pectic polysaccharide" and stored in a refrigerator. [Pg.638]

During the maceration, three products were distinguished (1) residual parenchyma, (2) pulp which consisted of free cells, and (3) juice which containted soluble pectins and oligouronides. Each of these products was estimated by its content of Alcohol Insoluble Solid (AIS). [Pg.957]

M, C, P and O are the weights of parenchyma, free cells, soluble pectin and oligouronides,... [Pg.960]

Figure 16.2. CV profiles for the oxidative desorption of by cycling the CeHe-modified Pt(lll) electrode in 0.05 M aq. HCIO4 (0.4-1.25 V range) after its transfer to the benzene-free cell (solid line 1st scan dotted line 5th scan dashed line unmodified Pt(l 11)) s = 20 mV s and T= 298 K. Figure 16.2. CV profiles for the oxidative desorption of by cycling the CeHe-modified Pt(lll) electrode in 0.05 M aq. HCIO4 (0.4-1.25 V range) after its transfer to the benzene-free cell (solid line 1st scan dotted line 5th scan dashed line unmodified Pt(l 11)) s = 20 mV s and T= 298 K.
In this case, there is a continuous supply of nutrients and a continuous withdrawal of the culture broth including the submerged free cells. The governing equations for continuous cultures are the same as the ones for fed-batch cultures (Equations 7.20-7.22). The only difference is that feed flowrate is normally equal to the effluent flowrate (Fm=Fout=F) and hence the volume. V, stays constant throughout the culture. [Pg.122]

Perfusion cultures of submerged free cells are essentially continuous cultures with a cell retention device so that no cells exit in the effluent stream. The governing ODEs are... [Pg.122]

Bleached (cholophyll free) cells without stigma but possesing paraflagellar body (PFB). [Pg.69]

The sol-gel-entrapped microbial cells have shown excellent tolerance to different alcohols [99], The immobilized E. coli cells followed the Michaelis-Menten equation when quantified with the (3-glucosidase activity via the hydrolysis of 4-nitrophenyl-(3-D-galactopyranosdie [142], The sol-gel matrices doped with gelatin prevented the cell lysis, which usually occurs during the initial gelation process [143], Microorganisms are now widely used in the biosorption of different pollutants and toxicants. Bacillus sphaericus JG-A12 isolated from uranium mining water has been entrapped in aqueous silica nanosol for the accumulation of copper and uranium [144], Premkumar et al. [145] immobilized recombinant luminous bacteria into TEOS sol-gel to study the effect of sol-gel conditions on the cell response (luminescence). The entrapped and free cells showed almost the same intensity of luminescence (little lower), but the entrapped cells were more stable than the free cells (4 weeks at 4°C). This kind of stable cell could be employed in biosensors in the near future. [Pg.545]

The assessment of reaction kinetics by means of batch tests may be strongly affected by dye adsorption on the biophase and supports. The relevance of the adsorption phenomena of dyes on biophase has been addressed in studies regarding free cells [41], granular support biofilm [24], entrapped cells [11, 18], anaerobic sludge [10,24,31,34] and biological activated carbon (BAC) [42,45,47,48]. They have pointed out that the kinetics may be overestimated if the assessment of the adsorption contribution to the dye removal is not taken into account. Under batch conditions, the dye is fastly split between the liquid phase and the biophase, resulting in a sharp reduction of the dye concentration in the liquid phase until adsorption equilibrium is approached. The rate of dye adsorption must be estimated and ruled out in the kinetic assessment. [Pg.113]

Aerobic phase. Technical air and liquid medium were continuously fed to the airlift during the aerobic phase. Gas flow rate was set at 5 nL/h corresponding to 0.64 vvm. The feeding rate of the phenol-bearing (200 mg/L) stream was set at 20 mL/h, that is D 0.15 h The dilution rate was set at a value larger than the maximum grow rate (wash-out conditions with respect to free cells), 0.14 h"1 [60]. [Pg.121]


See other pages where Free Cells is mentioned: [Pg.342]    [Pg.205]    [Pg.51]    [Pg.211]    [Pg.218]    [Pg.219]    [Pg.221]    [Pg.117]    [Pg.288]    [Pg.171]    [Pg.23]    [Pg.233]    [Pg.271]    [Pg.960]    [Pg.177]    [Pg.509]    [Pg.697]    [Pg.5]    [Pg.267]    [Pg.26]    [Pg.121]    [Pg.90]    [Pg.99]    [Pg.27]    [Pg.79]    [Pg.102]    [Pg.107]    [Pg.109]    [Pg.118]    [Pg.119]    [Pg.120]   


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Advantages of Free Radicals in the Cell

Amylases cell free

Animal cell lines serum-free medium

Biotransformations cell-free systems (isolated

Bubble-free liquid cell

Cancer cell-free nucleic acids

Carotene cell-free systems

Carotenoid biosynthesis cell-free systems

Cell Free diffusion

Cell Potential, Electrical Work, and Free Energy

Cell Potential, Free Energy, and the Equilibrium Constant

Cell free enzyme systems

Cell free preparations

Cell free systems mammalian cells

Cell free systems trypanosomes

Cell free systems yeast

Cell metabolism, free energy

Cell potential electrical work, and free

Cell potential reaction free energy

Cell voltage and free energy

Cell-Free Synthetic Systems for Metabolic Engineering and Biosynthetic Pathway Prototyping

Cell-Free System Stability

Cell-free assays

Cell-free assays 20-hydroxyecdysone activity

Cell-free assays 22-epz-ecdysone activity

Cell-free assays 5-deoxykaladasterone activity

Cell-free assays abutasterone activity

Cell-free assays activity

Cell-free assays ajugalactone activity

Cell-free assays ajugasterone C activity

Cell-free assays cyasterone activity

Cell-free assays ecdysone activity

Cell-free assays inokosterone activity

Cell-free assays makisterone A activity

Cell-free assays muristerone A activity

Cell-free assays ponasterone A activity

Cell-free assays poststerone activity

Cell-free assays systems

Cell-free assays turkesterone activity

Cell-free chromatin remodeling

Cell-free competition binding assay

Cell-free conversion

Cell-free enzyme synthesis

Cell-free experiments

Cell-free expression

Cell-free extracts

Cell-free extracts, experiments

Cell-free homogenates, preparation

Cell-free immunity

Cell-free layer

Cell-free nuclear assembly

Cell-free nuclear assembly proteins

Cell-free nuclear import

Cell-free nucleic acids

Cell-free oligosaccharide synthesis

Cell-free protein expression

Cell-free protein synthesis

Cell-free protein synthesis and

Cell-free screening

Cell-free synthesis

Cell-free systems

Cell-free systems amino acid dehydrogenases

Cell-free systems conjugation reactions

Cell-free systems properties

Cell-free systems redox reactions

Cell-free systems, vesicles studied

Cell-free transcription/translation system

Cell-free translation

Cell-free translation continuous flow system

Cell-free translation reticulocyte lysate

Cells cell-free scaffolds

Cells free amino acids

Challenges and Opportunities in Cell-Free Systems

Change of Free Enthalpy in Chemical Reactions Reversible Cell Voltage

Continuous-flow cell-free system

Cytoplasm-free cell envelopes

Doppler-free saturation cell

Drosophila cell-free extract

Drosophila cell-free nuclear assembly

Ergoline Biosynthesis in Cell-Free Extracts

Expression cell-free systems

Factors influencing the release of free radicals in cells and tissues

Fermentation, cell-free

Free Enthalpy and Cell Voltage

Free cell formation

Free energy cell potential, electrical work

Free energy cell voltage

Free energy change standard cell potential and

Free energy of cell reaction

Free space cell

Free-Radical Generation and Augmentation of Antioxidant Enzyme Activity in Vascular Endothelial Cells by Garlic

Fuel cell Gibbs free energy

How Much Free Arachidonate Is Produced in Cells

How do free radicals damage cells and tissues

Hyaluronic acid, cell-free synthesis

Initial Purification and Assay of Activities in Cell-Free

Kinase cell-free assay

Liquidlike cells free energy

Liquidlike cells free volume

Lysates, cell-free

Mercury-free cells

Mercury-free test cells

Method for adapting cells to serum-free medium

Microbial cell-free extracts

Microbial cell-free extracts enzymatic activity

NADPH oxidase cell-free activation system

Nuclear envelope cell-free systems

Oligosaccharides cell-free oligosaccharide synthesis

Patterns Cell-free Extracts

Poly -programmed cell-free systems

Prokaryotes cell wall-free

Protein synthesis cell-free systems

Protein synthesis fractionated cell-free systems

Protein synthesis in cell-free systems

Protein-free cell culture media

Proteus enzymes, cell-free

Recombinant protein cell-free system

Recombinant protein expression cell-free

Replication cell-free conditions

Sialyltransfer in Cells and Cell-Free Systems Cellular Location

Sperm cell-free systems

The Benefits of Cell-Free Systems

The Cell-Free Protein Expression Systems RTS

The Gibbs Free Energy and Cell Voltage

The Key to In Vitro Protein Evolution Cell-Free Translation

The Use of Cell-Free Protein Expression for NMR Analysis

The Use of Cell-Free Systems in Studying Saccharide Assembly Some Problems

Transcription Initiation on DNA Templates in Cell-Free Systems

Transcription and Translation in a Cell-Free System

Transcription cell-free

Translation in a cell-free system

Yeasts cell-free extract

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