[The interaction of alkylating derivatives of oligodeoxyribonucleotides and their methylphosphonate analogs with Mycoplasma cells]. 1991

L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'

Alkylating derivatives of decathymidylates and methylphosphonate analogs of oligodeoxyribonucleotides (MPAO) were studied for their interaction with cells of Acholeplasma laidlawii PG-8, Mycoplasma capricolum California Kid, M. pneumoniae FH and phytopathogenic strain (St. 118). It is shown that MPAO of octa- and hexadecathymidylates as well as decathymidylates 3'-terminal modified by phenazine and cholesterol groupings are sorbed by mycoplasma cells and can penetrate inside the cells. Efficiency of binding of alkylating derivatives and MPAO with mycoplasma cells depends on interaction time of reagents, their concentration in the reaction mixture and temperature.

UI MeSH Term Description Entries
D009174 Mycoplasma A genus of gram-negative, mostly facultatively anaerobic bacteria in the family MYCOPLASMATACEAE. The cells are bounded by a PLASMA MEMBRANE and lack a true CELL WALL. Its organisms are pathogens found on the MUCOUS MEMBRANES of humans, ANIMALS, and BIRDS. Eperythrozoon,Haemobartonella,Mycoplasma putrefaciens,PPLO,Pleuropneumonia-Like Organisms,Pleuropneumonia Like Organisms
D009177 Mycoplasma pneumoniae Short filamentous organism of the genus Mycoplasma, which binds firmly to the cells of the respiratory epithelium. It is one of the etiologic agents of non-viral primary atypical pneumonia in man. Eaton Agent
D009838 Oligodeoxyribonucleotides A group of deoxyribonucleotides (up to 12) in which the phosphate residues of each deoxyribonucleotide act as bridges in forming diester linkages between the deoxyribose moieties. Oligodeoxynucleotide,Oligodeoxyribonucleotide,Oligodeoxynucleotides
D009943 Organophosphorus Compounds Organic compounds that contain phosphorus as an integral part of the molecule. Included under this heading is broad array of synthetic compounds that are used as PESTICIDES and DRUGS. Organophosphorus Compound,Organopyrophosphorus Compound,Organopyrophosphorus Compounds,Compound, Organophosphorus,Compound, Organopyrophosphorus,Compounds, Organophosphorus,Compounds, Organopyrophosphorus
D010619 Phenazines
D002784 Cholesterol The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils. Epicholesterol
D004305 Dose-Response Relationship, Drug The relationship between the dose of an administered drug and the response of the organism to the drug. Dose Response Relationship, Drug,Dose-Response Relationships, Drug,Drug Dose-Response Relationship,Drug Dose-Response Relationships,Relationship, Drug Dose-Response,Relationships, Drug Dose-Response
D000128 Acholeplasma laidlawii An organism originally isolated from sewage, manure, humus, and soil, but recently found as a parasite in mammals and birds. Mycoplasma laidlawii
D000477 Alkylating Agents Highly reactive chemicals that introduce alkyl radicals into biologically active molecules and thereby prevent their proper functioning. Many are used as antineoplastic agents, but most are very toxic, with carcinogenic, mutagenic, teratogenic, and immunosuppressant actions. They have also been used as components in poison gases. Alkylating Agent,Alkylator,Alkylators,Agent, Alkylating,Agents, Alkylating
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships

Related Publications

L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
January 1989, Molekuliarnaia biologiia,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
March 1993, The Journal of biological chemistry,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
August 1989, FEBS letters,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
December 1990, Bioorganicheskaia khimiia,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
January 1989, Molekuliarnaia biologiia,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
January 1991, Nucleic acids symposium series,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
January 1995, Nucleic acids symposium series,
L P Panchenko, and O V Egorov, and A S Raĭt, and E M Ivanova, and N V Amirkhanov, and V F Zarytova, and V V Vlasov, and I G Skripal'
March 1992, FEBS letters,
Copied contents to your clipboard!