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1
Metabolic characterization of the viable, residually dividing and nondividing cell classes of recombination-deficient strains of Escherichia coli.大肠杆菌重组缺陷菌株中存活、仍在分裂和不再分裂细胞类别的代谢特征
J Bacteriol. 1977 Apr;130(1):160-6. doi: 10.1128/jb.130.1.160-166.1977.
2
The role of the rec genes in the viability of Escherichia coli K12.rec基因在大肠杆菌K12生存能力中的作用。
Basic Life Sci. 1975;5A:405-18. doi: 10.1007/978-1-4684-2895-7_56.
3
Analysis of the growth of recombination-deficient strains of Escherichia coli K-12.大肠杆菌K-12重组缺陷菌株生长情况分析。
J Bacteriol. 1974 Apr;118(1):242-9. doi: 10.1128/jb.118.1.242-249.1974.
4
Involvement of recombination genes in growth and viability of Escherichia coli K-12.重组基因与大肠杆菌K-12生长及生存能力的关系。
J Bacteriol. 1971 Apr;106(1):204-12. doi: 10.1128/jb.106.1.204-212.1971.
5
Biochemical and genetic studies of recombination proficiency in Escherichia coli. II. Rec+ revertants caused by indirect suppression of rec- mutations.大肠杆菌中重组能力的生化与遗传学研究。II. 由rec-突变的间接抑制导致的Rec+回复突变体
Proc Natl Acad Sci U S A. 1970 Sep;67(1):128-35. doi: 10.1073/pnas.67.1.128.
6
Isolation of the nonviable cells produced during normal growth of recombination-deficient strains of Escherichia coli K-12.大肠杆菌K-12重组缺陷菌株正常生长过程中产生的无活力细胞的分离。
J Bacteriol. 1973 Sep;115(3):928-36. doi: 10.1128/jb.115.3.928-936.1973.
7
Characteristics of some multiply recombination-deficient strains of Escherichia coli.一些多重重组缺陷型大肠杆菌菌株的特征
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8
Recombinant F' factors from Escherichia coli K-12 strains carrying recB or recC.来自携带recB或recC的大肠杆菌K-12菌株的重组F'因子。
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9
Phospholipase activity in bacteriophage-infected Escherichia coli. III. Phopholipase A involvement in lysis of T4-infected cells.噬菌体感染的大肠杆菌中的磷脂酶活性。III. 磷脂酶A参与T4感染细胞的裂解。
J Virol. 1975 Oct;16(4):867-71. doi: 10.1128/JVI.16.4.867-871.1975.
10
Dark-recovery processes in Escherichia coli irradiated with ultraviolet light. 3. Effect of rec mutations on recovery of excision-deficient mutants of Escherichia coli K-12.紫外线照射大肠杆菌后的暗修复过程。3. rec突变对大肠杆菌K-12切除缺陷型突变体恢复的影响。
J Bacteriol. 1970 May;102(2):404-10. doi: 10.1128/jb.102.2.404-410.1970.

引用本文的文献

1
Essential Role for an Isoform of Escherichia coli Translation Initiation Factor IF2 in Repair of Two-Ended DNA Double-Strand Breaks.大肠杆菌翻译起始因子 IF2 同工型在修复双链 DNA 末端断裂中的重要作用。
J Bacteriol. 2022 Apr 19;204(4):e0057121. doi: 10.1128/jb.00571-21. Epub 2022 Mar 28.
2
Isolation of a recombination-deficient mutant of Rhodopseudomonas capsulata.荚膜红假单胞菌重组缺陷突变体的分离。
J Bacteriol. 1984 Dec;160(3):971-5. doi: 10.1128/jb.160.3.971-975.1984.
3
Recombinant levels of Escherichia coli K-12 mutants deficient in various replication, recombination, or repair genes.缺乏各种复制、重组或修复基因的大肠杆菌K-12突变体的重组水平。
J Bacteriol. 1978 Jun;134(3):958-66. doi: 10.1128/jb.134.3.958-966.1978.
4
Inactivation of prophage in ultraviolet-irradiated Escherichia coli: dependence on recA gene activity.紫外线照射的大肠杆菌中前噬菌体的失活:对recA基因活性的依赖性。
J Bacteriol. 1979 Dec;140(3):848-51. doi: 10.1128/jb.140.3.848-851.1979.
5
Early events and mechanisms in the induction of bacterial SOS functions: analysis of the phage repressor inactivation process in vivo.细菌SOS功能诱导中的早期事件及机制:体内噬菌体阻遏物失活过程分析
Proc Natl Acad Sci U S A. 1978 Apr;75(4):1657-61. doi: 10.1073/pnas.75.4.1657.

本文引用的文献

1
A proposal for a uniform nomenclature in bacterial genetics.细菌遗传学统一命名法的提议。
Genetics. 1966 Jul;54(1):61-76. doi: 10.1093/genetics/54.1.61.
2
Pleiotropic effect of the rec A gene of Escherichia coli: uncoupling of cell division from deoxyribonucleic acid replication.大肠杆菌rec A基因的多效性作用:细胞分裂与脱氧核糖核酸复制的解偶联
J Bacteriol. 1971 May;106(2):539-42. doi: 10.1128/jb.106.2.539-542.1971.
3
Involvement of recombination genes in growth and viability of Escherichia coli K-12.重组基因与大肠杆菌K-12生长及生存能力的关系。
J Bacteriol. 1971 Apr;106(1):204-12. doi: 10.1128/jb.106.1.204-212.1971.
4
An ATP-dependent deoxyribonuclease from Escherichia coli with a possible role in genetic recombination.一种来自大肠杆菌的依赖ATP的脱氧核糖核酸酶,可能在基因重组中发挥作用。
Proc Natl Acad Sci U S A. 1969 Dec;64(4):1292-9. doi: 10.1073/pnas.64.4.1292.
5
Biochemical and genetic studies of recombination proficiency in Escherichia coli. I. Enzymatic activity associated with recB+ and recC+ genes.大肠杆菌中重组能力的生化与遗传学研究。I. 与recB+和recC+基因相关的酶活性。
Proc Natl Acad Sci U S A. 1970 Apr;65(4):955-61. doi: 10.1073/pnas.65.4.955.
6
Genetic analysis of recombination-deficient mutants of Escherichia coli K-12 carrying rec mutations cotransducible with thyA.携带与thyA共转导的rec突变的大肠杆菌K-12重组缺陷型突变体的遗传分析。
J Bacteriol. 1969 Nov;100(2):923-34. doi: 10.1128/jb.100.2.923-934.1969.
7
Characteristics of some multiply recombination-deficient strains of Escherichia coli.一些多重重组缺陷型大肠杆菌菌株的特征
J Bacteriol. 1969 Oct;100(1):231-9. doi: 10.1128/jb.100.1.231-239.1969.
8
Spontaneous lethal sectoring, a further feature of Escherichia coli strains deficient in the function of rec and uvr genes.自发致死性扇形区形成,是rec和uvr基因功能缺陷的大肠杆菌菌株的另一个特征。
J Bacteriol. 1968 Sep;96(3):652-9. doi: 10.1128/jb.96.3.652-659.1968.
9
Genetic location of certain mutations conferring recombination deficiency in Escherichia coli.大肠杆菌中某些导致重组缺陷的突变的基因定位。
J Bacteriol. 1969 Jan;97(1):244-9. doi: 10.1128/jb.97.1.244-249.1969.
10
Formation of merodiploids in matings with a class of Rec- recipient strains of Escherichia coli K12.在与一类大肠杆菌K12 Rec-受体菌株交配时形成部分二倍体。
Proc Natl Acad Sci U S A. 1968 May;60(1):160-7. doi: 10.1073/pnas.60.1.160.

大肠杆菌重组缺陷菌株中存活、仍在分裂和不再分裂细胞类别的代谢特征

Metabolic characterization of the viable, residually dividing and nondividing cell classes of recombination-deficient strains of Escherichia coli.

作者信息

Miller J E, Barbour S D

出版信息

J Bacteriol. 1977 Apr;130(1):160-6. doi: 10.1128/jb.130.1.160-166.1977.

DOI:10.1128/jb.130.1.160-166.1977
PMID:323225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC235188/
Abstract

The abilities of rec+, recB- recC-, recA-, and recA- recB- rec C- strains to support growth of bacteriophage T4, to take up oxygen, and to maintain cell integrity have been measured. (i) With respect to bacteriophage T4 growth, T4 phage is produced with identical lysis time in single -step growth curves with all strains tested. rec- strains show reduced phage production (fewer infected centers), but the average burst size per infected center is the same for all strains tested. Some rec- cells are unable to produce any phage, whereas the remainder of the rec-cells produce phage as rapidly and as efficiently as rec+ cells. (ii) With respect to oxygen consumption, rec- strains are deficient relative to the rec+ control to the same extent as the deficiency in phage production by theculture. The reduction in oxygen consumption is coordinate with reduction in rate of mass increase of the rec- culture. (iii) With respect to cell integrity, rec- cultures show increased lysis as measured by release of beta-galactosidase into the medium. The kinetics of release suggest that rec- nondividing cells all eventually lyse. These results are most consistent with the idea that rec- residually dividing cells and viable cells are metabolically normal according to the parameters we have measured, whereas nondividing cells are metabolically inactive.

摘要

已测定rec⁺、recB⁻ recC⁻、recA⁻以及recA⁻ recB⁻ recC⁻菌株支持噬菌体T4生长、摄取氧气和维持细胞完整性的能力。(i) 关于噬菌体T4生长,在所有测试菌株的一步生长曲线中,T4噬菌体产生时的裂解时间相同。rec⁻菌株显示噬菌体产量降低(感染中心较少),但每个感染中心的平均爆发量对于所有测试菌株而言是相同的。一些rec⁻细胞无法产生任何噬菌体,而其余rec⁻细胞产生噬菌体的速度和效率与rec⁺细胞相同。(ii) 关于氧气消耗,rec⁻菌株相对于rec⁺对照的缺陷程度与培养物中噬菌体产量的缺陷程度相同。氧气消耗的减少与rec⁻培养物质量增加速率的降低是协同的。(iii) 关于细胞完整性,通过β-半乳糖苷酶释放到培养基中的量来衡量,rec⁻培养物显示出增加的裂解。释放动力学表明rec⁻非分裂细胞最终都会裂解。这些结果与以下观点最为一致:根据我们测量的参数,rec⁻残余分裂细胞和活细胞在代谢上是正常的,而非分裂细胞在代谢上是无活性的。