Sequence-specific DNA modification in Acetobacter xylinum.

Two cryptic plasmids have been discovered in Acetobacter xylinum B42 and in its derivative PEA-1, a cellulose defective mutant. These two plasmids were designated pAX1 and pAX2 (50 and 105 kb in size, respectively). A restriction map was constructed for pAX1. Attempts to cure these plasmids were uns...

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Autores principales: Petroni, E.A., Bocca, S.N., Ielpi, L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_01455680_v42_n5_p759_Petroni
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spelling todo:paper_01455680_v42_n5_p759_Petroni2023-10-03T14:59:58Z Sequence-specific DNA modification in Acetobacter xylinum. Petroni, E.A. Bocca, S.N. Ielpi, L. bacterial DNA endodeoxyribonuclease ApoI type II site specific deoxyribonuclease article genetics Gluconacetobacter xylinus isolation and purification mutation nucleotide sequence plasmid restriction mapping Base Sequence Deoxyribonuclease EcoRI Deoxyribonucleases, Type II Site-Specific DNA, Bacterial Gluconacetobacter xylinus Mutation Plasmids Restriction Mapping Two cryptic plasmids have been discovered in Acetobacter xylinum B42 and in its derivative PEA-1, a cellulose defective mutant. These two plasmids were designated pAX1 and pAX2 (50 and 105 kb in size, respectively). A restriction map was constructed for pAX1. Attempts to cure these plasmids were unsuccessful. Enzyme restriction analysis showed that these plasmids contain protected EcoRI and ApoI sites. Using Southern blot and hybridization techniques, the protection was extended to chromosomal DNA. Enzyme restriction analysis of several plasmids, from different origins and containing different incompatibility groups, isolated from strain PEA-1 also showed EcoRI and ApoI protection. The presence of modifications on specific sequences was not found in A. xylinum 8747. These results strongly suggest the presence of a modification system in A. xylinum B42 that recognizes the tetranucleotide 5'-AATT. Fil:Petroni, E.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bocca, S.N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Ielpi, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01455680_v42_n5_p759_Petroni
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic bacterial DNA
endodeoxyribonuclease ApoI
type II site specific deoxyribonuclease
article
genetics
Gluconacetobacter xylinus
isolation and purification
mutation
nucleotide sequence
plasmid
restriction mapping
Base Sequence
Deoxyribonuclease EcoRI
Deoxyribonucleases, Type II Site-Specific
DNA, Bacterial
Gluconacetobacter xylinus
Mutation
Plasmids
Restriction Mapping
spellingShingle bacterial DNA
endodeoxyribonuclease ApoI
type II site specific deoxyribonuclease
article
genetics
Gluconacetobacter xylinus
isolation and purification
mutation
nucleotide sequence
plasmid
restriction mapping
Base Sequence
Deoxyribonuclease EcoRI
Deoxyribonucleases, Type II Site-Specific
DNA, Bacterial
Gluconacetobacter xylinus
Mutation
Plasmids
Restriction Mapping
Petroni, E.A.
Bocca, S.N.
Ielpi, L.
Sequence-specific DNA modification in Acetobacter xylinum.
topic_facet bacterial DNA
endodeoxyribonuclease ApoI
type II site specific deoxyribonuclease
article
genetics
Gluconacetobacter xylinus
isolation and purification
mutation
nucleotide sequence
plasmid
restriction mapping
Base Sequence
Deoxyribonuclease EcoRI
Deoxyribonucleases, Type II Site-Specific
DNA, Bacterial
Gluconacetobacter xylinus
Mutation
Plasmids
Restriction Mapping
description Two cryptic plasmids have been discovered in Acetobacter xylinum B42 and in its derivative PEA-1, a cellulose defective mutant. These two plasmids were designated pAX1 and pAX2 (50 and 105 kb in size, respectively). A restriction map was constructed for pAX1. Attempts to cure these plasmids were unsuccessful. Enzyme restriction analysis showed that these plasmids contain protected EcoRI and ApoI sites. Using Southern blot and hybridization techniques, the protection was extended to chromosomal DNA. Enzyme restriction analysis of several plasmids, from different origins and containing different incompatibility groups, isolated from strain PEA-1 also showed EcoRI and ApoI protection. The presence of modifications on specific sequences was not found in A. xylinum 8747. These results strongly suggest the presence of a modification system in A. xylinum B42 that recognizes the tetranucleotide 5'-AATT.
format JOUR
author Petroni, E.A.
Bocca, S.N.
Ielpi, L.
author_facet Petroni, E.A.
Bocca, S.N.
Ielpi, L.
author_sort Petroni, E.A.
title Sequence-specific DNA modification in Acetobacter xylinum.
title_short Sequence-specific DNA modification in Acetobacter xylinum.
title_full Sequence-specific DNA modification in Acetobacter xylinum.
title_fullStr Sequence-specific DNA modification in Acetobacter xylinum.
title_full_unstemmed Sequence-specific DNA modification in Acetobacter xylinum.
title_sort sequence-specific dna modification in acetobacter xylinum.
url http://hdl.handle.net/20.500.12110/paper_01455680_v42_n5_p759_Petroni
work_keys_str_mv AT petroniea sequencespecificdnamodificationinacetobacterxylinum
AT boccasn sequencespecificdnamodificationinacetobacterxylinum
AT ielpil sequencespecificdnamodificationinacetobacterxylinum
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