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Download PDF by Yuzaburo Ishida (auth.), Ronald P. Kiene, Pieter T.: Biological and Environmental Chemistry of DMSP and Related

By Yuzaburo Ishida (auth.), Ronald P. Kiene, Pieter T. Visscher, Maureen D. Keller, Gunter O. Kirst (eds.)

ISBN-10: 0306453061

ISBN-13: 9780306453069

ISBN-10: 146130377X

ISBN-13: 9781461303770

''An crucial ebook for individuals operating within the sector of sulfur compounds within the atmosphere and will be in all institutional libraries....Well listed, good presented.'' --- SGM Quarterly, November 1997 ''Extremely important and well-produced symposium quantity that are meant to be of curiosity to many environmental scientists, microbial and plant physiologists, and aquatic ecologists.'' The Quarterly evaluate of Biology, June 1998

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Extra info for Biological and Environmental Chemistry of DMSP and Related Sulfonium Compounds

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Rhodes. 1995. Identification of quaternary ammonium and tertiary sulfonium compounds by plasma desorption mass spectrometry. 1. Mass Spectrom. (in press) 4. Gorham, 1.. 1. Coughlan, R. G. Wyn-lones. 1981. Estimation of quaternary ammonium and tertiary sulfonium compounds by thin layer electrophoresis and scanning reflectance densitometry. 1. Chromatogr. 210: 550-554. 5. Grone, T. O. Kirst. 1992. The effect of nitrogen deficiency, methionine and inhibitors of methionine metabolism on the DMSP contents of Tetraselmis subcordiformis (Stein) Mar.

3 ng) produces a strong MH+ ion (Figure 6). A sodium adduct, [M+Nar, is also detected at mlz 157. Because carrier solvents containing high ionic strength buffers or salts can interfere with the electrospray ionization process, it is likely that some sample cleanup will always be necessary prior to analysis of DMSP samples. Detection limits for ESI-MS analysis of DMSP are remarkable; reasonable signals are obtained even from low fmoll/-ll solutions (data not shown). Thus, the sensitivity of ESI-MS is sufficient to detect DMSP directly in seawater, but it is likely that some microscale desalting procedure will have to developed before this mass spectrometric technique can be used for this purpose.

Methylthioadenosine. Adv. Enzymol. 54: 195-265. 70. , R. Chillemi, R. Morrone, A. Patti and M. Piattelli. 1989. Dragendorff-positive compounds in some Mediterranean red algae. Biochcm. System. Ecol. 17: 5-10. 71. Shapiro S. K. and A. J. Ferro. 1977. Metabolism of adenosylmethionine during the life cycles of Enterobacter aerogenes and Saccharomyces cerevisae, pp. 58-82. In F. Salvatore. E. Borek, V. Zappia. H. G. Williams-Ashman and F. Schlenk (cds), The Biochemistry of Adenosylmethionine. Columbia University Press, New York.

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Biological and Environmental Chemistry of DMSP and Related Sulfonium Compounds by Yuzaburo Ishida (auth.), Ronald P. Kiene, Pieter T. Visscher, Maureen D. Keller, Gunter O. Kirst (eds.)


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