Biochemistry papers

Biochemistry papers 1956 Bimonthly 500 American Institute of Biological Sciences (NSF)c 15 10 to libraries of academic institutions... 

Xanthopterin monohydrate (2-amino-4,6-dihydroxypteridine, 2-amino-pteridin-4,6(lff,5ff)-dione) [5979-01-1 (H2O), 119-48-8 (anhydr)] M 197.2, m <300", pK, 1.6 (basic), pKj 6.59 (acidic), PK3 9.31 (acidic)(anhydrous species), and pKj 1.6 (basic), pK2 8.65 (acidic), PK3 9.99 (acidic)(7,8-hydrated species). Purification as for isoxanthopterin. Crystd by acidifying an ammoniacal soln, and collecting by centrifugation followed by washing with EtOH, ether and drying at 100° in vacuo. Paper chromatography Rp 0.15 ( -PrOH, 1% aq NH3, 2 1), 0.36 ( -BuOH,AcOH, H2O, 4 1 1) and 0.47 (3% aq NH3). [Inoue and Perrin J Chem Soc 260 7962 Inoue Tetrahedron 20 243 I964 see also Blakley Biochemistry of Folic Acid and Related Pteridines North Holland Publ Co, Amsterdam 1969.]... 

Qnadroni, M., et al., 1996. Analy.sis of global re.spon.ses by protein and peptide fingerprinting of protein.s i.solated by two-dimensional electrophore-.sis. Application to snlfate-starvation re.sponse of Escherichia coli. European Journal of Biochemistry 239 773-781. This paper de.scribes the n.se of tandem MS in the analysis of protein.s in cell extracts. 

On the basis of the luciferin-luciferase reaction discovered by Dubois (1887), Michelson, Henry and their associates studied the biochemistry of the Pholas bioluminescence for several years beginning in 1970 (Michelson, 1978). They isolated, purified, and characterized the luciferin and the luciferase, and published about a dozen papers in which the luciferin isolated was referred to as Pholas luciferin. Since the luciferin is clearly a protein, later authors called it pholasin following the traditional way of naming a photoprotein... 

Schoenfeld-Tacher, R., Persichitte, K. A., Jones, L. L. (2001). Relation of student characteristics to learning of basic biochemistry concepts from a multimedia goal-based scenario. Paper presented at the annual meeting of the American Educational Research Association, New Orleans, LA (ERIC Document Reproduction Service No. ED 440 875). 

Methodological Surveys in Biochemistry and Analysis, vol. 20. Royal Society of Chemistry. Scientific American (1981) Issue on industrial microbiology, vol. 245, No. 3. (An excellent series of papers describing the manufacture by microorganisms or products useful to mankind.)... 

Following the adoption of azolides as valuable and versatile reagents in synthetic organic chemistry,[1] and also in the context of their potential role in biochemistry, a great many kinetic, mechanistic, and theoretical papers appeared concerning this group of compounds and their properties. Some of these papers[18],[20] are very useful for a better understanding of the reactivity of azolides. 

Presented below are brief descriptions of some of the applications to structure analysis to which each of the three advanced methods are making important contributions. For the reader who wishes to learn more about these methods and applications a list of recent reviews and other leading references to these applications is also included. The titles of the papers that we have referenced will make it clear that we have tried to include applications of relevance not only to organometallic chemistry but also to biochemistry and related fields. 

The cited papers in the field of biochemistry and microbiology can contribute to find better composing technology to reach higher decomposition rate using optimal temperature, time, and grinding the materials that help to reduce the survival of pathogens and ammonia loss. 

The title of a Nature paper by the Amory Houghton Professor of Chemistry and Biochemistry at Harvard University, Jeremy R. Knowles (Knowles, 1991). 

Kinoshita, T. and Okamoto, K. (1977). Paper presented at the 36th Annual Meeting of the Chemical Society of Japan, Osaka, April. Pre-prints, II, p. 847 Kirsh, J. F. and Hubbard, C. D. (1972). Biochemistry 11,2483... 

The use of isotopes in biochemistry, particularly radioisotopes, took off after World War II. Developments in electronics and nuclear energy, and the construction of piles in the U.S. and the U.K., enormously improved the production and detection of radioisotopes. At the same time the introduction of paper and ion-exchange chromatography (Chapter 10) revolutionized analytical methods for the separation of low molecular weight compounds, enabling intermediates to be separated rapidly, identified, and estimated. By 1945 strategies for the evaluation of metabolic pathways and cycles were familiar, thanks to the work of Krebs and the pre-war German schools. 

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