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1.
ORGYN ; (4): 2-5, 1994.
Article in English | MEDLINE | ID: mdl-12288144

ABSTRACT

PIP: The Alan Guttmacher Institute emerged from the Planned Parenthood of America's Center for Family Planning Program Development in 1968. It split from Planned Parenthood in 1977 because some foundations would not fund an entity linked to Planned Parenthood. The Institute originally focused on women and contraception but has expanded to include abortion, sexually transmitted diseases, and the changing family. Its mission is to influence public policy to work towards reproductive freedom and to be an unimpeachable source of accurate data on reproductive and sexual health. Its 55-member staff works out of New York City and Washington D.C. Its 1993 budget was only $4.7 million. Its 3 divisions cover public policy, research, and publishing. The Institute determines what research projects to undertake based on what question it wants to answer. The goal of research revolves around changing public policy or public opinion. It obtains funding from a foundation or the government for each research project. Possible donors are not always willing to fund projects, however. For example, the Institute wanted to examine funding of reproductive health care by private medical insurance and first went to possible donors 5 years ago. It was finally funded in 1994 because of the interest in health care reform. Much of staff time is spent writing proposals rather than on research. The Institute does not accept money from any organization that may gain financially from the outcome of the research. Its research activities allow the Institute to achieve its goal of providing thorough information on reproductive health. The Institute has 2 staff members who deal only with requests for information, which they can usually provide or help to provide. The Institute is becoming more international. The staff is rather young and has high morale and a high energy level.^ieng


Subject(s)
Health Planning , Organizations , Public Policy , Reproductive Medicine , Americas , Developed Countries , Family Planning Services , Health , North America , United States
2.
Orig Life Evol Biosph ; 15: 77-88, 1985.
Article in English | MEDLINE | ID: mdl-11539613

ABSTRACT

The effect of adsorbed ions and pH on the adsorption of several purine and pyrimidine nucleotides on montmorillonite was studied. The cations used to prepare homoionic montmorillonite was Na+, Mn2+, Fe3+, Co2+, Ni+, Cu2+, and Zn2+. The nucleotides studied were 5'-,3'-, and 2'-AMP, and 5'-CMP in the pH range 2 through 12. The results show that preferential adsorption amongst nucleotides and similar molecules is dependent upon pH and the nature of the substituted metal cation in the clay. At neutral pH, it was observed that 5'-AMP was more strongly adsorbed than 2'AMP, 3'-AMP, and 5'-CMP. Cu2+ and Zn2+ clays showed enhanced adsorption of 5'-AMP compared to the other cation clays studied in the pH range 4-8. Below pH 4, the adsorption is attributed to cation and anion exchange adsorption mechanisms: above pH 4, anion exchange may also occur, but the adsorption (when it occurs) likely depends on a complexation mechanism occurring between metal cation in the clay exchange site the biomolecule. It is thus proposed that homoionic clays may have played a significant role in the concentration mechanism of biomonomers in the prebiotic environment, a prerequisite step necessary for the formation of biopolymers in the remaining steps leading to the origin of life.


Subject(s)
Adenosine Monophosphate/chemistry , Bentonite/chemistry , Cytidine Monophosphate/chemistry , Evolution, Chemical , Zinc/chemistry , Adsorption , Cations, Monovalent , Copper , Hydrogen-Ion Concentration , Metals
3.
J Mol Evol ; 17(2): 69-77, 1981.
Article in English | MEDLINE | ID: mdl-7253037

ABSTRACT

NMR spectral studies on the HCN oligomers suggest the presence of carboxamide and urea groupings. The release of CO2, H2O, HCN, CH3CN, HCONH2 and pyridine on pyrolysis is consistent with the presence of these groupings as well as carboxylic acid groups. No basic primary amine groupings could be detected with fluorescamine. Hydrazinolysis of the HCN oligomers releases 10% of the amino acids normally released by acid hydrolysis. The oligomers give a positive biuret test but this is not due to the presence of peptide bonds. There is no conclusive evidence for the presence of peptide bonds in the HCN oligomers. No diglycine was detected on partial hydrolysis of the HCN oligomers at pH 8.5 suggesting that HCN oligomers were not a source of prebiotic peptides.


Subject(s)
Biological Evolution , Cyanates , Amino Acids , Chemical Phenomena , Chemistry , Magnetic Resonance Spectroscopy , Purines , Pyrimidines , Urea
4.
J Mol Evol ; 13(4): 317-30, 1979 Nov.
Article in English | MEDLINE | ID: mdl-229235

ABSTRACT

The reaction of 0.1 M HCN and dilute solutions of diaminomaleonitrile (DAMN) at pH 8--9 and 25 degrees C in the presence of suspensions of montmorillonite (bentonite) clays were investigated. Montmorillonite clays inhibit the oligomerization of aqueous solutions of HCN. Yields of colored oligomers, ura, and DAMN, are all diminished by clays, but the rate of loss of cyanide is not significantly decreased. The inhibition of oligomer formation is due to the clay-catalyzed decomposition of DAMN. The absence of strong binding of DAMN to clays was suggested by our failure to detect DAMN when a clay that had been incubated with DAMN was washed with spermidine (6 x 10(-3) g/liter). It was established that DAMN does not simply bind to the clays by the observation that the bulk of the radioactivity was recovered from the supernatant in the reaction of 14C-DAMN with montmorillonite. The clay-catalyzed decomposition of DAMN was observed when montmorillonite from two different sources was used and with a variety of homoinic montmorillonites and bentonites. A modification of the established procedure for using the cyanide electrode for cyanide analyses was used to follow the release of HCN from DAMN. This new method can be used in both the acidic and basic pH range and it does not result in the destruction of DAMN by the reagents used for the analysis. Quantitative analyses of the reaction solution from the clay-catalyzed decomposition of DAMN revealed the formation of 1--2 equivalents of HCN per mole of DAMN. The possible significance of these clay-catalyzed reactions in chemical evolution is discussed.


Subject(s)
Bentonite , Hydrogen Cyanide , Chemical Phenomena , Chemistry , Cyanides/analysis , Diamines , Nitriles , Urea
5.
J Chromatogr ; 174(2): 409-19, 1979 Jul 01.
Article in English | MEDLINE | ID: mdl-546898

ABSTRACT

The high-performance liquid chromatographic separation of a large variety of nucleic acid constituents on a silica-based, weak-anion exchange column was accomplished. Using this technique it was possible to achieve some relatively difficult separations, such as the separation of 2'-, 3'-, and 5'-AMP, and the separation of a mixture of ribo- and deoxyribo-nucleosides and -nucleotides. A number of other separations are demonstrated by isocratic or gradient elution. These include the separation of a mixture of nucleoside monophosphates, the separation of a mixture of nucleoside mono-, di-, and triphosphates, the separation of a mixture of nucleosides and bases, and the separation of a mixture of nucleotide oligomers. These chromatographic separations were accomplished using relatively simple experimental procedures at ambient temperatures and involved relatively short analysis times. Excellent separations were obtained, in most cases, by adjustment of buffer concentration and pH, or by addition of an organic modifier. In some cases, it was necessary to use gradient elution to achieve optimum resolution.


Subject(s)
Nucleic Acids/analysis , Animals , Chromatography, High Pressure Liquid , Chromatography, Ion Exchange , Liver/analysis , Mice , Mice, Inbred BALB C , Nucleosides/isolation & purification , Nucleotides/isolation & purification , Purines/isolation & purification , Pyrimidines/isolation & purification
6.
J Mol Evol ; 11(4): 293-311, 1978 Oct 06.
Article in English | MEDLINE | ID: mdl-31491

ABSTRACT

Dilute (0.1 M) solutions of HCN condense to oligomers at pH 9.2. Hydrolysis of these oligomers yields 4,5-dihydroxypyrimidine, orotic acid, 5-hydroxyuracil, adenine, 4-aminoimidazole-5-carboxamide and amino acids. These results, together with the earlier data, demonstrate that the three main classes of nitrogen-containing biomolecules, purines, pyrimidines and amino acids may have originated from HCN on the primitive earth. The observation of orotic acid and 4-aminoimidazole-5-carboxyamide suggests that the contemporary biosynthetic pathways for nucleotides may have evolved from the compounds released on hydrolysis of HCN oligomers.


Subject(s)
Amino Acids/chemical synthesis , Hydrogen Cyanide , Purines/chemical synthesis , Pyrimidines/chemical synthesis , Hydrogen-Ion Concentration , Hydrolysis , Orotic Acid , Oxygen , Water
8.
Science ; 181(4096): 248-9, 1973 Jul 20.
Article in English | MEDLINE | ID: mdl-17730933

ABSTRACT

This summer, in cooperation with the Mexican government's National Council of Science and Technology, the AAAS marked its 125th anniversary with a special meeting in Mexico City, the association's first in Latin America. For the occasion, News and Comment asked Edward Edelson, a science writer for the New York Daily News who has covered previous AAAS meetings, to review the Mexico City gathering from a reporter's point of view. A second article by Robert Gillette of the News and Comment staff will elaborate on the objectives of the meeting and on the difficulties of organizing a major international conference.

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