Loading…

A nucleoside triphosphate-dependent deoxyribonuclease from Bacillus laterosporus. The mode of action of the enzyme

The acid-soluble products of exhaustive digestion of native DNA with Bacillus laterosporus DNase consist of 6.5% of mononucleotides and 93.5% of oligonucleotides with an average chain length of 3.2. The results of viscometric studies and inactivation of transforming DNA indicate the existence of aci...

Full description

Saved in:
Bibliographic Details
Published in:Journal of biochemistry (Tokyo) 1975-07, Vol.78 (1), p.115-121
Main Authors: Anai, M, Yamanaka, M, Shibata, T, Mihara, T, Nishimoto, T
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 121
container_issue 1
container_start_page 115
container_title Journal of biochemistry (Tokyo)
container_volume 78
creator Anai, M
Yamanaka, M
Shibata, T
Mihara, T
Nishimoto, T
description The acid-soluble products of exhaustive digestion of native DNA with Bacillus laterosporus DNase consist of 6.5% of mononucleotides and 93.5% of oligonucleotides with an average chain length of 3.2. The results of viscometric studies and inactivation of transforming DNA indicate the existence of acid-insoluble intermediates and the selective degradation of the population of substrate molecules rather than a random nucleolytic action. Furthermore, sucrose density gradient analysis of partially digested DNA showed that the initial DNA added as a substrate disappeared progressively during the reaction, being replaced by much more slowly sedimenting acid-insoluble materials, which were eventually degraded into acid-soluble end products during the reaction; products intermediate in size between these two components were not detectable. Studies with DNA labeled at the 3'-terminus indicate that Bacillus laterosporus DNase does not attack DNA from 3'-hydroxyl ends to yeild acid-soluble or acid-insoluble materials in a random manner. The results presented in this paper indicate that the nature of the attack of B. laterosporus nuclease is similar to that previously proposed for Micrococcus luteus DNase. The possibility of the sequential release of acid-insoluble intermediate fragments as well as acid-soluble products from the terminal portion of DNA by the enzyme is discussed.
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_83079772</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>83079772</sourcerecordid><originalsourceid>FETCH-LOGICAL-p206t-bc30e05052d08f77ba2b7365e30a433d6cbc662472c963177aae66f676d516853</originalsourceid><addsrcrecordid>eNotkD1PwzAQhj2ASin8BCRPbEGOndjJWCqgSJVYisQWOfZFMXLi4A-J8OtJodO99-q5Z7gLtCaE5llNi48rdB3C52mljK3QKs_rghbVGvktHpOy4ILRgKM3U-_C1MsImYYJRg1jxBrc9-xN6_5QGQB33g34USpjbQrYLrhfzpxP4QEfe8CDW2yuw1JF48ZTiksL4888wA267KQNcHueG_T-_HTc7bPD28vrbnvIJkp4zFrFCJCSlFSTqhOilbQVjJfAiCwY01y1inNaCKpqznIhpATOOy64LnNelWyD7v-9k3dfCUJsBhMUWCtHcCk0FSOiFoIu4N0ZTO0Aupm8GaSfm_OT2C9c3WPS</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>83079772</pqid></control><display><type>article</type><title>A nucleoside triphosphate-dependent deoxyribonuclease from Bacillus laterosporus. The mode of action of the enzyme</title><source>J-STAGE (Japan Science &amp; Technology Information Aggregator, Electronic) Freely Available Titles - English</source><source>Oxford University Press:Jisc Collections:Oxford Journal Archive: Access period 2024-2025</source><creator>Anai, M ; Yamanaka, M ; Shibata, T ; Mihara, T ; Nishimoto, T</creator><creatorcontrib>Anai, M ; Yamanaka, M ; Shibata, T ; Mihara, T ; Nishimoto, T</creatorcontrib><description>The acid-soluble products of exhaustive digestion of native DNA with Bacillus laterosporus DNase consist of 6.5% of mononucleotides and 93.5% of oligonucleotides with an average chain length of 3.2. The results of viscometric studies and inactivation of transforming DNA indicate the existence of acid-insoluble intermediates and the selective degradation of the population of substrate molecules rather than a random nucleolytic action. Furthermore, sucrose density gradient analysis of partially digested DNA showed that the initial DNA added as a substrate disappeared progressively during the reaction, being replaced by much more slowly sedimenting acid-insoluble materials, which were eventually degraded into acid-soluble end products during the reaction; products intermediate in size between these two components were not detectable. Studies with DNA labeled at the 3'-terminus indicate that Bacillus laterosporus DNase does not attack DNA from 3'-hydroxyl ends to yeild acid-soluble or acid-insoluble materials in a random manner. The results presented in this paper indicate that the nature of the attack of B. laterosporus nuclease is similar to that previously proposed for Micrococcus luteus DNase. The possibility of the sequential release of acid-insoluble intermediate fragments as well as acid-soluble products from the terminal portion of DNA by the enzyme is discussed.</description><identifier>ISSN: 0021-924X</identifier><identifier>PMID: 1194248</identifier><language>eng</language><publisher>England</publisher><subject>Bacillus - enzymology ; Deoxyribonucleases - analysis ; Deoxyribonucleases - metabolism ; DNA, Bacterial - isolation &amp; purification ; DNA, Bacterial - metabolism ; Nucleotides - pharmacology ; Oligodeoxyribonucleotides - analysis ; Viscosity</subject><ispartof>Journal of biochemistry (Tokyo), 1975-07, Vol.78 (1), p.115-121</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1194248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anai, M</creatorcontrib><creatorcontrib>Yamanaka, M</creatorcontrib><creatorcontrib>Shibata, T</creatorcontrib><creatorcontrib>Mihara, T</creatorcontrib><creatorcontrib>Nishimoto, T</creatorcontrib><title>A nucleoside triphosphate-dependent deoxyribonuclease from Bacillus laterosporus. The mode of action of the enzyme</title><title>Journal of biochemistry (Tokyo)</title><addtitle>J Biochem</addtitle><description>The acid-soluble products of exhaustive digestion of native DNA with Bacillus laterosporus DNase consist of 6.5% of mononucleotides and 93.5% of oligonucleotides with an average chain length of 3.2. The results of viscometric studies and inactivation of transforming DNA indicate the existence of acid-insoluble intermediates and the selective degradation of the population of substrate molecules rather than a random nucleolytic action. Furthermore, sucrose density gradient analysis of partially digested DNA showed that the initial DNA added as a substrate disappeared progressively during the reaction, being replaced by much more slowly sedimenting acid-insoluble materials, which were eventually degraded into acid-soluble end products during the reaction; products intermediate in size between these two components were not detectable. Studies with DNA labeled at the 3'-terminus indicate that Bacillus laterosporus DNase does not attack DNA from 3'-hydroxyl ends to yeild acid-soluble or acid-insoluble materials in a random manner. The results presented in this paper indicate that the nature of the attack of B. laterosporus nuclease is similar to that previously proposed for Micrococcus luteus DNase. The possibility of the sequential release of acid-insoluble intermediate fragments as well as acid-soluble products from the terminal portion of DNA by the enzyme is discussed.</description><subject>Bacillus - enzymology</subject><subject>Deoxyribonucleases - analysis</subject><subject>Deoxyribonucleases - metabolism</subject><subject>DNA, Bacterial - isolation &amp; purification</subject><subject>DNA, Bacterial - metabolism</subject><subject>Nucleotides - pharmacology</subject><subject>Oligodeoxyribonucleotides - analysis</subject><subject>Viscosity</subject><issn>0021-924X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1975</creationdate><recordtype>article</recordtype><recordid>eNotkD1PwzAQhj2ASin8BCRPbEGOndjJWCqgSJVYisQWOfZFMXLi4A-J8OtJodO99-q5Z7gLtCaE5llNi48rdB3C52mljK3QKs_rghbVGvktHpOy4ILRgKM3U-_C1MsImYYJRg1jxBrc9-xN6_5QGQB33g34USpjbQrYLrhfzpxP4QEfe8CDW2yuw1JF48ZTiksL4888wA267KQNcHueG_T-_HTc7bPD28vrbnvIJkp4zFrFCJCSlFSTqhOilbQVjJfAiCwY01y1inNaCKpqznIhpATOOy64LnNelWyD7v-9k3dfCUJsBhMUWCtHcCk0FSOiFoIu4N0ZTO0Aupm8GaSfm_OT2C9c3WPS</recordid><startdate>197507</startdate><enddate>197507</enddate><creator>Anai, M</creator><creator>Yamanaka, M</creator><creator>Shibata, T</creator><creator>Mihara, T</creator><creator>Nishimoto, T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>197507</creationdate><title>A nucleoside triphosphate-dependent deoxyribonuclease from Bacillus laterosporus. The mode of action of the enzyme</title><author>Anai, M ; Yamanaka, M ; Shibata, T ; Mihara, T ; Nishimoto, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p206t-bc30e05052d08f77ba2b7365e30a433d6cbc662472c963177aae66f676d516853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1975</creationdate><topic>Bacillus - enzymology</topic><topic>Deoxyribonucleases - analysis</topic><topic>Deoxyribonucleases - metabolism</topic><topic>DNA, Bacterial - isolation &amp; purification</topic><topic>DNA, Bacterial - metabolism</topic><topic>Nucleotides - pharmacology</topic><topic>Oligodeoxyribonucleotides - analysis</topic><topic>Viscosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anai, M</creatorcontrib><creatorcontrib>Yamanaka, M</creatorcontrib><creatorcontrib>Shibata, T</creatorcontrib><creatorcontrib>Mihara, T</creatorcontrib><creatorcontrib>Nishimoto, T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biochemistry (Tokyo)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anai, M</au><au>Yamanaka, M</au><au>Shibata, T</au><au>Mihara, T</au><au>Nishimoto, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A nucleoside triphosphate-dependent deoxyribonuclease from Bacillus laterosporus. The mode of action of the enzyme</atitle><jtitle>Journal of biochemistry (Tokyo)</jtitle><addtitle>J Biochem</addtitle><date>1975-07</date><risdate>1975</risdate><volume>78</volume><issue>1</issue><spage>115</spage><epage>121</epage><pages>115-121</pages><issn>0021-924X</issn><abstract>The acid-soluble products of exhaustive digestion of native DNA with Bacillus laterosporus DNase consist of 6.5% of mononucleotides and 93.5% of oligonucleotides with an average chain length of 3.2. The results of viscometric studies and inactivation of transforming DNA indicate the existence of acid-insoluble intermediates and the selective degradation of the population of substrate molecules rather than a random nucleolytic action. Furthermore, sucrose density gradient analysis of partially digested DNA showed that the initial DNA added as a substrate disappeared progressively during the reaction, being replaced by much more slowly sedimenting acid-insoluble materials, which were eventually degraded into acid-soluble end products during the reaction; products intermediate in size between these two components were not detectable. Studies with DNA labeled at the 3'-terminus indicate that Bacillus laterosporus DNase does not attack DNA from 3'-hydroxyl ends to yeild acid-soluble or acid-insoluble materials in a random manner. The results presented in this paper indicate that the nature of the attack of B. laterosporus nuclease is similar to that previously proposed for Micrococcus luteus DNase. The possibility of the sequential release of acid-insoluble intermediate fragments as well as acid-soluble products from the terminal portion of DNA by the enzyme is discussed.</abstract><cop>England</cop><pmid>1194248</pmid><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-924X
ispartof Journal of biochemistry (Tokyo), 1975-07, Vol.78 (1), p.115-121
issn 0021-924X
language eng
recordid cdi_proquest_miscellaneous_83079772
source J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - English; Oxford University Press:Jisc Collections:Oxford Journal Archive: Access period 2024-2025
subjects Bacillus - enzymology
Deoxyribonucleases - analysis
Deoxyribonucleases - metabolism
DNA, Bacterial - isolation & purification
DNA, Bacterial - metabolism
Nucleotides - pharmacology
Oligodeoxyribonucleotides - analysis
Viscosity
title A nucleoside triphosphate-dependent deoxyribonuclease from Bacillus laterosporus. The mode of action of the enzyme
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T09%3A41%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20nucleoside%20triphosphate-dependent%20deoxyribonuclease%20from%20Bacillus%20laterosporus.%20The%20mode%20of%20action%20of%20the%20enzyme&rft.jtitle=Journal%20of%20biochemistry%20(Tokyo)&rft.au=Anai,%20M&rft.date=1975-07&rft.volume=78&rft.issue=1&rft.spage=115&rft.epage=121&rft.pages=115-121&rft.issn=0021-924X&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E83079772%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p206t-bc30e05052d08f77ba2b7365e30a433d6cbc662472c963177aae66f676d516853%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=83079772&rft_id=info:pmid/1194248&rfr_iscdi=true