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Bacteria analysis

Reschiglian, P. Zattoni, A. Cinque, L. Roda, B. Dal Piaz, F. Roda, A. Moon, M. H. Min, B. R. Hollow-fiber flow field-flow fractionation for whole bacteria analysis by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Anal. Chem. 2004, 76,2103-2111. [Pg.149]

Rondon, M. R., Raffel, S. J., Goodman, R. M., Handelsman, J. Toward functional genomics in bacteria Analysis of gene expression in Escherichia coli from a bacterial artificial chromosome library of Bacillus cereus. Proc. Natl. Acad. Sci. USA 1999, 96, 6451-6455. [Pg.186]

Marti nez-Garcia, E. and de Lorenzo, V. (2011) Engineering multiple genomic deletions in gram-negative bacteria analysis of the multi-resistant antibiotic profile of Pseudomonas putida KT2440. Environ. Microbiol., 13 (10), 2702 - 2716. [Pg.319]

Hayes JM, Murray KK. Ambient laser ablation sample transfer with nanostructure-assisted laser desorption ionization mass spectrometry for bacteria analysis. Rapid Commun Mass Spectrom. [Pg.10]

Abdelhamid HN, Gopal J, Wu HF. Synthesis and application of ionic liquid matrices (ILMs) for effective pathogenic bacteria analysis in matrix assisted laser desorption/ionization (MALDl-MS). Analytica Chimica Acta. 2013 767 104-11. doi 10.1016/j.aca.2012.12.054. [Pg.65]

Abdelliamid HN, Bhaisare ML, Wu HF. Ceria nanocubic-ultiasonication assisted dispersive liquid-liquid microextraction coupled with matrix assisted laser desorption/ionizalion mass spectrometry for pathogenic bacteria analysis. Talanta. 2014 120 208-17. [Pg.170]

Gedda G, Abdelhamid HN, Khan MS, Wu HF. ZnO nanoparticle-modified polymethyl methacrylate-assisted dispersive liquid-liquid microextraction coupled with MALDI-MS for rapid pathogenic bacteria analysis. Rsc Adv. 2014 4(86) 45973-83. [Pg.173]

False positive results cf fecal coliform bacteria analysis have been obtained that may be caused by a variety cf different organisms including Klebsiella and coliforms from sources other than humans and animals. [Pg.106]

Nutritional dependence on pterinoid antimetabolites is a fascinating phenomenon and part of the problem of resistance to the antifolics in cancer therapy. Law (1958) noted that some strains of mouse leukemia have become dependent on antifolics. Is the explanation like that for Neurospora If one had antifolio-dependent strains of protozoa and bacteria, analysis of their growth requirements might uncover new metabolites, as happened for streptomycin-dependent bacteria. [Pg.43]

By changing the enzyme and mediator, the amperometric sensor in Figure 11.39 is easily extended to the analysis of other substrates. Other bioselective materials may be incorporated into amperometric sensors. For example, a CO2 sensor has been developed using an amperometric O2 sensor with a two-layer membrane, one of which contains an immobilized preparation of autotrophic bacteria. As CO2 diffuses through the membranes, it is converted to O2 by the bacteria, increasing the concentration of O2 at the Pt cathode. [Pg.520]

After a desired clone is obtained and mapped with restriction enzymes, further analysis usually depends on the deterrnination of its nucleotide sequence. The nucleotide sequence of a new gene often provides clues to its function and the stmcture of the gene product. Additionally, the DNA sequence of a gene provides a guidepost for further manipulation of the sequence, for example, lea ding to the production of a recombinant protein in bacteria. [Pg.233]

Microscopists in every technical field use the microscope to characterize, compare, and identify a wide variety of substances, eg, protozoa, bacteria, vimses, and plant and animal tissue, as well as minerals, building materials, ceramics, metals, abrasives, pigments, foods, dmgs, explosives, fibers, hairs, and even single atoms. In addition, microscopists help to solve production and process problems, control quaUty, and handle trouble-shooting problems and customer complaints. Microscopists also do basic research in instmmentation, new techniques, specimen preparation, and appHcations of microscopy. The areas of appHcation include forensic trace evidence, contamination analysis, art conservation and authentication, and asbestos control, among others. [Pg.328]

In all antiseptic testing, it is recognized that skin and mucous membranes to which products ate appHed cannot be disinfected or sterilized but it is possible to significantly reduce the population of transient and resident pathogenic bacterial flora. AH in vivo test methods requite a deterrnination of the bacteria on the skin before and after treatment. Because of the normal variation in bacterial population of the skin of different people, a number of people must be tested in order to make a statistical analysis of the results. Different parts of the body are used for different tests. In aH of the tests the details of the protocol ate extremely important and must be strictly adhered to in order to obtain reproducible results. [Pg.140]

TABLE 6.3 Typical Microbiological Analysis at Outlet A Main Condenser Suffering No Significant Corrosion by Sulfate-Reducing Bacteria ... [Pg.129]

Clostridia frequently are found where sulfate-reducing bacteria are present, often in high numbers inside tubercles. A typical microbiological analysis of tubercular material removed from a troubled service water system main is given in Table 6.4. Clostridia counts above 10 /g of material are high enough to cause concern. When acid producers... [Pg.136]

Microbiological analysis of material removed from corroded areas showed high aerobic and relatively high anaerobic counts (Table 6.7). Fungi counts were also elevated, indicating relatively high die-off of aerobic bacteria that is, the coolant was approaching its useful life. [Pg.156]

The water analysis is incomplete unless the number of coliform bacteria present is determined as well. A multiple-tube fermentation technique can be used to enumerate positive presumptive, confirmed, and fecal coliform tests. Results of the tests are expressed in terms of the most probable number (MPN). That is, the count is based on a statistical analysis of sets of tubes in a series of serial dilutions. MPN is related to a sample volume of 100 ml. Thus, an MPN of 10 means 10 coliforms per 100 ml of water. [Pg.462]

Methoxatin, now known as coenzyme PQQ, was originally obtained from methylotrophic bacteria but is now known to be a mammalian cofactor, for example, for lysyl oxidase and dopamine p-hydroxylase. The first synthesis of this rare compound was accomplished by the route outlined below. In the retrosynthetic analysis both of the heterocyclic rings were disconnected using directly keyed transforms. [Pg.141]

In terms of amino acids bacterial protein is similar to fish protein. The yeast s protein is almost identical to soya protein fungal protein is lower than yeast protein. In addition, SCP is deficient in amino acids with a sulphur bridge, such as cystine, cysteine and methionine. SCP as a food may require supplements of cysteine and methionine whereas they have high levels of lysine vitamins and other amino acids. The vitamins of microorganisms are primarily of the B type. Vitamin B12 occurs mostly hi bacteria, whereas algae are usually rich in vitamin A. The most common vitamins in SCP are thiamine, riboflavin, niacin, pyridoxine, pantothenic acid, choline, folic acid, inositol, biotin, B12 and P-aminobenzoic acid. Table 14.4 shows the essential amino acid analysis of SCP compared with several sources of protein. [Pg.339]

Background current, 21, 65 Background subtraction, 40, 106 Bacteria electrode, 182 Band microelectrodes, 130, 135 Beryllium, 82 Bienzyme electrodes, 175 Biocatalytic devices, 172 Biological recognition, 171 Biosensors, 50, 171 Bipotentiostat, 106 Blood electrolyte, 165 Boltzmann equation, 19 Brain analysis, 40, 116 Butler-Volmer equation, 14... [Pg.205]


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See also in sourсe #XX -- [ Pg.258 , Pg.259 , Pg.260 , Pg.261 ]

See also in sourсe #XX -- [ Pg.247 ]




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