Synthesis and Characterization of Poly-8-Methylamino-Adenylic.

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dc.contributor.authorElekwa, Iheanyichukwu
dc.contributor.otherFalayan, J.O.
dc.date.accessioned2014-08-25T10:46:55Z
dc.date.accessioned2018-10-29T10:56:07Z
dc.date.available2014-08-25T10:46:55Z
dc.date.available2018-10-29T10:56:07Z
dc.date.issued1987
dc.degree.awardM.Sc. Biochemistryen_US
dc.departmentBiochemistryen_US
dc.description.abstractA polynucleotide, poly-8-methylamino adenylic acid, was synthesized and hybridized with poly U. Adenosine-5-monophosphate purchased from BDN Chemical Corporation was brominated with bromine in Na-acetate buffer pH 3.9, stirred for 24 hours. The excess bromine was removed with some drops of concentrated sodium sulphite solution. It was then evaporated to dryness, on a rotatory evaporator at 37 oC and characterised. The product 8-Bromo-adenosine-5-Monphosphate, was methylaminated with methylamine in water, and refluxed for 48 hours at 65oC on an oil bath. Excess methylamine was removed with dilute sulphuric acid, while the product was evaporated to dryness and characterized. The synthesized methylamino adenosine-5-monophosphate was converted to its diphosphate analogue by the phophoro-morpholidate process. Orthophosphoric acid was used to introduce the phosphate group. The converted methylamino-adenosine-5-diphosphate was polymerized with the enzyme polynucleotide phophorylase PNPase, (EC 2.7.7.8) from Micrococcus luteus that was purchased from Boehringner Chemical Corporation. This enzyme PNPase is only specific for the diphosphate form. The polymerization was carried out in a reaction medium of MgCl2.6H2O EDTA (Ethylene diaminetetra-acetic acid) and tris buffer pH 9.0. It was incubated for 21 hours at 36oC, and characterized. The Poly-8-methyamino adenylic acid so synthesized was hybridized with poly U purchased from BDH- Chemical Corporation. The Job’s continuous variation method in KH2PO4 + K2HPO4 buffer pH 7.00 at 37oC was adopted. The polymer formed at 1:1 hybrid with Poly U. This satisfies some of the requirements for synthetic polynucleotide inducers. Some physico-chemical methods used in the characterization, included infra-red, ultra-violet, proton nuclear magnestic resonance and chromatographic methods. Complete UV spectra were recorded in the range of 200-400nm on Sp 8-400 (uv/vis) spectrophotometer. The infra-red spectra recorded using a sodium chloride cell in the range of 200-4000 cm-1 on Sp 3 -300 infra-red spectrophotometer. And, the Proton Nuclear Magnetic Resonance was recorded on Perkin Elmer Spectrophometer. The spots on the paper chromatography were detected and developed under UV light (at 254 nm wavelength).en_US
dc.facultiesScienceen_US
dc.format.filetypepdfen_US
dc.identifier.citationAPAen_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3299
dc.language.isoenen_US
dc.pages.totalpages134pen_US
dc.publisherObafemi Awolowo Universityen_US
dc.subjectPolynucleotideen_US
dc.subjectpoly Uen_US
dc.subjectbromineen_US
dc.subjectevaporationen_US
dc.subjectpolymerizationen_US
dc.subjectenzyme PNPaseen_US
dc.subjectchromatographyen_US
dc.subjectspectrometeren_US
dc.titleSynthesis and Characterization of Poly-8-Methylamino-Adenylic.en_US
dc.typeThesisen_US
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