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Sterilizing System

All additions such as the inoculums, nutrients, pH control solutions, or gases (carbon dioxide/nitrogen wherever required) and the source of oxygen must be completely sterile. Air as the source of oxygen has to be continuously fed. This must be filtered through a suitable hydrophobic, fuUy sterihzable filter to remove all types of bacteria/ vimses. Steam at 0.4-0.5 MPa abs is generally used as the sterilizing medium. [Pg.296]


Fermenter An industrial microbiological reactor in which the addition of nutrients, removal of products, and insertion of measuring sensors and control devices are maintained while accessories like heating, aeration, agitation, and sterilization systems are provided. [Pg.903]

Figure 1.1. Schematic diagram of instrumentation associated with a fermentor. The steam sterilization system and all sensors and transmitters are omitted for clarity. Solid lines represent process streams. Hairlines represent information flow. Figure 1.1. Schematic diagram of instrumentation associated with a fermentor. The steam sterilization system and all sensors and transmitters are omitted for clarity. Solid lines represent process streams. Hairlines represent information flow.
The certification activities include a series of process documentation and qualification studies that start with the initial installation of a sterilization system and continue as process engineering changes or new or revised product introductions are required. Qualification activities comprise installation, operational, change, and performance phases. [Pg.270]

All alarm features available on the sterilizer system under consideration,... [Pg.277]

Figure 10.2 Continuous sterilizing systems, (a) Heat exchanger and continuous steam injection and (b) heat exchanger and indirect heater. Figure 10.2 Continuous sterilizing systems, (a) Heat exchanger and continuous steam injection and (b) heat exchanger and indirect heater.
Rate Enhancement by Urease The enzyme urease enhances the rate of urea hydrolysis at pH 8.0 and 20 °C by a factor of 1014. If a given quantity of urease can completely hydrolyze a given quantity of urea in 5.0 min at 20 °C and pH 8.0, how long would it take for this amount of urea to be hydrolyzed under the same conditions in the absence of urease Assume that both reactions take place in sterile systems so that bacteria cannot attack the urea. [Pg.234]

Two types of dry-heat sterilization systems are utilized in the pharmaceutical industry today. They are the conventional hot air oven and the tunnel system. The major difference between the two systems, as far as validation is concerned, is the belt or line speed variable with the tunnel system. [Pg.142]

An automated machine has been developed for sterilization of medical, surgical, and dental instruments. It uses buffered peracetic acid liquid of 0.1-0.5% concentration. Peracetic acid sterilization systems have been adopted for hemodialyzers. The food processing and beverage industries use peracetic acid extensively because the breakdown products in high dilution do not produce objectionable odor, taste, or toxicity. Since rinsing is not necessary in this use, time and money are saved. [Pg.1165]

Matsunaga, T., Tomoda, T., Nakajima, T., Nakamura, N. and Komine, T. (1988) Continuous-sterilization system that uses photosemiconductor powders. Appl. Environ. Microbiol. 54, 1330-1333. [Pg.470]

The steam sterilization system (see Figures 5-9) used by S.G.D. Serail is designed with autoclave -type vessel construction to resist sterilization pressure combined with a control system permitting the validation of the sterilization cycles and eventual determination of the experimental FO sterilization value. [Pg.428]

The experimental data were examined to determine whether any correlation exists between variations in the experimental procedures and the efficiency of the ozone sterilization system. It can be concluded that there was no definite correlation among the flow rate of the gas stream, per cent concentration of ozone in the gas stream, and... [Pg.383]

It is possible that Gottschalk and Buehler (1912) carried out the oxidation with an excess of oxygen which would not occur in nature at the oxidation interface of a mineral deposit. Granger and Warren (1969) conducted experiments to investigate the oxidation of iron sulphides by an aerobic aqueous phase in a sterile system. The objective was to study the formation of unstable intermediate ions during the oxidation process. The intermediate sulphur species detected were sulphite and thiosulphate. In general these products are more easily oxidised than the metallic sulphides and are stable only if removed from the oxidising environment. [Pg.251]

It is instructive to calculate ASO - H20(%o), which is the difference between the 5 0 values of sol and H2O in mine water (Fig. 12.22). In the absence of isotope fractionation and with Fe as the oxidant, a zero difference would be expected. Taylor et al. (1984b) propose that Fe dominates pyrite oxidation in submersed environments. For such conditions ASO - H20(%o) values exceed zero due to isotope fractionation, ranging from about 4 to 6 in sterile systems to about 11 in the presence of T. ferrooxidans. Fractionation is caused by the greater reactivity of light 0 than heavy 0, with thus favored in product sulfate. Bacterial activity (in this case T. ferrooxidans) causes more fractionation than takes place in the abiotic oxidation reaction. ASO - H20(% ) values range up to about 18 when O2 is the chief oxidant in the presence of bacteria. S uch conditions are expected in aerated streams and in shallow unsaturated materials (Taylor et al. 1984a, 1984b). [Pg.463]

Since this early discovery there has been considerable appreciation for the role of the soil microbial community in pesticide transformations. In some cases the role of microorganisms has been stressed by comparison of degradation rates in natural and sterilized systems (32), while in others researchers have chosen to use isolation of pesticide-degrading microorganisms from soil sis evidence of microbial involvement (33). It has also been recognized that environmental conditions that influence microbial activity (temperature, moisture,...) affect the microbial degradation of pesticides in soil (34). The importance of microbial involvement is demonstrated by the many reviews of pesticide/microbe interactions that have appeared (35-41). [Pg.6]

Hinata, K., and N. Konno. 1979. Studies on a male sterile system having B. campestris nucleus and D. muralis cytoplasm. Breeding and some characteristics of this strain. Japanese Journal of Breeding 29 305-311. [Pg.59]

Riungu, T.C., and P.B.E. McVetty. 2003. Inheritance of maintenance and restoration of the Diplotaxis muralis (mur) cytoplasmic male sterility system in summer rape. Canadian Journal of Plant Science 83 515-518. [Pg.60]

Dealkylation appears to be a common transformation pathway for agrochemicals with the requisite functionality however, the reaction mechanisms for this process have not been thoroughly investigated. The lack of reactivity often observed in sterile systems has led to the general conclusion that reductive dealkylation requires the presence of viable microorganisms. Examples of N-dealkylation include the dealkylation of carbofuran (Equation 3.45) (Hassall, 1982) and atrazine, which may... [Pg.196]


See other pages where Sterilizing System is mentioned: [Pg.328]    [Pg.176]    [Pg.173]    [Pg.417]    [Pg.372]    [Pg.208]    [Pg.247]    [Pg.470]    [Pg.471]    [Pg.391]    [Pg.279]    [Pg.2454]    [Pg.3515]    [Pg.3523]    [Pg.77]    [Pg.80]    [Pg.268]    [Pg.215]    [Pg.222]    [Pg.53]    [Pg.54]    [Pg.75]    [Pg.90]    [Pg.676]    [Pg.159]    [Pg.59]    [Pg.67]    [Pg.518]    [Pg.179]    [Pg.182]    [Pg.293]   


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