在cooktomeat培养基中保存的R12(CM, SM, SA)因子的自然消失和非传递性变异

隆勝 中嶋, 鈴木 ミツヱ, 三男 亀田, 賢治 原田, 進 三橋
{"title":"在cooktomeat培养基中保存的R12(CM, SM, SA)因子的自然消失和非传递性变异","authors":"隆勝 中嶋, 鈴木 ミツヱ, 三男 亀田, 賢治 原田, 進 三橋","doi":"10.3412/JSB.25.345","DOIUrl":null,"url":null,"abstract":"Escherichia coli K-12 F- harboring R12 (CM. SM. SA) factor was stored in cooked meat medium at room temperature. After 3 years, it was examined for loss of R factor, as well as the genetic properties of this factor. It was found that 90.5% of surviving cells had lost their R factor to be sensitive to chloramphenicol (CM), streptomycin (SM), and sulfanilamide (SA). In the other surviving cells retaining their R factor, no segregation was noticed among resistance markers, So long as examined. Two derivative R factors, R12-5 and R12-22, were proveed to be nontransferable by conjugation, indicating that transferable (tra+) R12 factor had mutated to tra- R factor by storage in cooked meat medium for along time. From the results of a curing experiment and transduction to the rec- strain, it was clarified that the tra- R factors, R12-5 and R12-22, existed extrachromosomally and were replicated (rep+) autonomously in their host. Genetic studies revealed that R12-5 and R12-22 factors were ifm+ (inhibition of F-mating) and irs+ (interference of R factor superinfection), as well as the original R12 factor was. Reversion took place from tra- to tra+ at a frequency of 8.0 to 8.8×10-10, indicating that these were point mutants of the tra loci. The E. coli K-12 strain carrying either tra- R12-5 or tra- R12-22 acquired an ability to transfer its nontransferable R factor by complementation in cooperation with F factor, chromosomal F of the Hfr strain, or with transferable R factor.","PeriodicalId":14812,"journal":{"name":"Japanese journal of bacteriology","volume":"34 1","pages":"345-349"},"PeriodicalIF":0.0000,"publicationDate":"1970-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"クックトミート培地に保存中に見られたR12(CM・SM・SA)因子の自然消失と非伝達性変異\",\"authors\":\"隆勝 中嶋, 鈴木 ミツヱ, 三男 亀田, 賢治 原田, 進 三橋\",\"doi\":\"10.3412/JSB.25.345\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Escherichia coli K-12 F- harboring R12 (CM. SM. SA) factor was stored in cooked meat medium at room temperature. After 3 years, it was examined for loss of R factor, as well as the genetic properties of this factor. It was found that 90.5% of surviving cells had lost their R factor to be sensitive to chloramphenicol (CM), streptomycin (SM), and sulfanilamide (SA). In the other surviving cells retaining their R factor, no segregation was noticed among resistance markers, So long as examined. Two derivative R factors, R12-5 and R12-22, were proveed to be nontransferable by conjugation, indicating that transferable (tra+) R12 factor had mutated to tra- R factor by storage in cooked meat medium for along time. From the results of a curing experiment and transduction to the rec- strain, it was clarified that the tra- R factors, R12-5 and R12-22, existed extrachromosomally and were replicated (rep+) autonomously in their host. Genetic studies revealed that R12-5 and R12-22 factors were ifm+ (inhibition of F-mating) and irs+ (interference of R factor superinfection), as well as the original R12 factor was. Reversion took place from tra- to tra+ at a frequency of 8.0 to 8.8×10-10, indicating that these were point mutants of the tra loci. The E. coli K-12 strain carrying either tra- R12-5 or tra- R12-22 acquired an ability to transfer its nontransferable R factor by complementation in cooperation with F factor, chromosomal F of the Hfr strain, or with transferable R factor.\",\"PeriodicalId\":14812,\"journal\":{\"name\":\"Japanese journal of bacteriology\",\"volume\":\"34 1\",\"pages\":\"345-349\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1970-07-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Japanese journal of bacteriology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3412/JSB.25.345\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese journal of bacteriology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3412/JSB.25.345","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

大肠杆菌k - 12f -携带R12 (CM)。SM。SA)因子在熟肉培养基中室温保存。3年后,检查R因子的丢失,以及该因子的遗传特性。90.5%的存活细胞失去R因子,对氯霉素(CM)、链霉素(SM)和磺胺(SA)敏感。在其他保留R因子的存活细胞中,没有发现抗性标记之间的分离。2个衍生R因子R12-5和R12-22经偶联证实是不可转移的,说明可转移(tra+) R12因子在熟肉培养基中长期储存已突变为tra- R因子。通过对rec-菌株的处理实验和转导结果,证实了R12-5和R12-22存在于染色体外,并在宿主体内自主复制(rep+)。遗传学研究表明,R12-5和R12-22因子为ifm+(抑制f -交配)和irs+(干扰R因子重叠感染),原始R12因子为ifm+(抑制f -交配)。从tra-到tra+以8.0到8.8×10-10的频率发生逆转,表明这些是tra位点的点突变体。携带tra- R12-5或tra- R12-22的大肠杆菌K-12菌株通过与Hfr菌株的F因子、染色体F或可转移R因子的互补,获得了转移其不可转移R因子的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
クックトミート培地に保存中に見られたR12(CM・SM・SA)因子の自然消失と非伝達性変異
Escherichia coli K-12 F- harboring R12 (CM. SM. SA) factor was stored in cooked meat medium at room temperature. After 3 years, it was examined for loss of R factor, as well as the genetic properties of this factor. It was found that 90.5% of surviving cells had lost their R factor to be sensitive to chloramphenicol (CM), streptomycin (SM), and sulfanilamide (SA). In the other surviving cells retaining their R factor, no segregation was noticed among resistance markers, So long as examined. Two derivative R factors, R12-5 and R12-22, were proveed to be nontransferable by conjugation, indicating that transferable (tra+) R12 factor had mutated to tra- R factor by storage in cooked meat medium for along time. From the results of a curing experiment and transduction to the rec- strain, it was clarified that the tra- R factors, R12-5 and R12-22, existed extrachromosomally and were replicated (rep+) autonomously in their host. Genetic studies revealed that R12-5 and R12-22 factors were ifm+ (inhibition of F-mating) and irs+ (interference of R factor superinfection), as well as the original R12 factor was. Reversion took place from tra- to tra+ at a frequency of 8.0 to 8.8×10-10, indicating that these were point mutants of the tra loci. The E. coli K-12 strain carrying either tra- R12-5 or tra- R12-22 acquired an ability to transfer its nontransferable R factor by complementation in cooperation with F factor, chromosomal F of the Hfr strain, or with transferable R factor.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
In memoriam of Dr. Yoshiro Terawaki Typings of Campylobacter jejuni isolated from patients of 2 outbreak cases by genotypic and phenotypic methods ベロ毒素産生 Escherichia coli O157:H7に対する Bicozamycin の抗菌作用 内毒素の活性中心(リピドA)の研究 Campylobacter infection in Japan.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1