Mass biological

The capital cost of most aqueous waste treatment operations is proportional to the total flow of wastewater, and the operating cost increases with decreasing concentration for a given mass of contaminant to be removed. Thus, if two streams require different treatment operations, it makes no sense to mix them and treat both streams in both treatment operations. This will increase both capital and operating costs. Rather, the streams should be segregated and treated separately in a distributed effluent treatment system. Indeed, effective primary treatment might mean that some streams do not need biological treatment at all. 

W. V. Ligon, Jr., Evaluating the Composition of Liquid Surfaces Using Mass Spectrometry, in Biological Mass Spectrometry, Elsevier, Amsterdam, 1990. 

Protein tertiary structure is also influenced by the environment In water a globu lar protein usually adopts a shape that places its hydrophobic groups toward the interior with Its polar groups on the surface where they are solvated by water molecules About 65% of the mass of most cells is water and the proteins present m cells are said to be m their native state—the tertiary structure m which they express their biological activ ity When the tertiary structure of a protein is disrupted by adding substances that cause the protein chain to unfold the protein becomes denatured and loses most if not all of Its activity Evidence that supports the view that the tertiary structure is dictated by the primary structure includes experiments m which proteins are denatured and allowed to stand whereupon they are observed to spontaneously readopt their native state confer matron with full recovery of biological activity... 

For mixture.s the picture is different. Unless the mixture is to be examined by MS/MS methods, usually it will be necessary to separate it into its individual components. This separation is most often done by gas or liquid chromatography. In the latter, small quantities of emerging mixture components dissolved in elution solvent would be laborious to deal with if each component had to be first isolated by evaporation of solvent before its introduction into the mass spectrometer. In such circumstances, the direct introduction, removal of solvent, and ionization provided by electrospray is a boon and puts LC/MS on a level with GC/MS for mixture analysis. Further, GC is normally concerned with volatile, relatively low-molecular-weight compounds and is of little or no use for the many polar, water soluble, high-molecular-mass substances such as the peptides, proteins, carbohydrates, nucleotides, and similar substances found in biological systems. LC/MS with an electrospray interface is frequently used in biochemical research and medical analysis. 

Dass, C., Principles and Practice of Biological Mass Spectrometry, Wiley, Chichester, U.K., 2000. 

Matsuo, T., Caprioli, R.M., Gross, M.L., and Seyama, Y, Biological Mass Spectrometry Present and Future, Wiley, New York, 1994. 

Analytical Biochemistry Analytical Chemistry Analytical Instrumentation Applied Spectroscopy Reviews Biological Mass Spectrometry... 

Apart from the well-known journals covering aspects of chemistry, physics, biology, medicine, geology, environmental science, electrical engineering, and forensic science, which all have occasional articles that use mass spectrometry for analytical purposes, the following journals frequently contain papers in which mass spectrometry plays a major role ... 

Monobasic acids are determined by gas chromatographic analysis of the free acids dibasic acids usually are derivatized by one of several methods prior to chromatographing (176,177). Methyl esters are prepared by treatment of the sample with BF.—methanol, H2SO4—methanol, or tetramethylammonium hydroxide. Gas chromatographic analysis of silylation products also has been used extensively. Liquid chromatographic analysis of free acids or of derivatives also has been used (178). More sophisticated hplc methods have been developed recentiy to meet the needs for trace analyses ia the environment, ia biological fluids, and other sources (179,180). Mass spectral identification of both dibasic and monobasic acids usually is done on gas chromatographicaHy resolved derivatives. 

R. H. Doi and M. McGloughlin, Biology of Bacilli Applications to Industry Butterworth-Heinemaim, Stoneham, Mass., 1992. 

A review pubHshed ia 1984 (79) discusses some of the methods employed for the determination of phenytoia ia biological fluids, including thermal methods, spectrophotometry, luminescence techniques, polarography, immunoassay, and chromatographic methods. More recent and sophisticated approaches iaclude positive and negative ion mass spectrometry (80), combiaed gas chromatography—mass spectrometry (81), and ftir immunoassay (82). 

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