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1
Duplication-translocations of tryptophan operon genes in Escherichia coli.大肠杆菌中色氨酸操纵子基因的重复易位
J Bacteriol. 1973 Oct;116(1):33-40. doi: 10.1128/jb.116.1.33-40.1973.
2
Genetic and segregation analysis of Escherichia coli strains containing a tandem duplication of the trpD-purB region of the chromosome.含有染色体trpD-purB区域串联重复的大肠杆菌菌株的遗传与分离分析。
J Bacteriol. 1978 Feb;133(2):650-60. doi: 10.1128/jb.133.2.650-660.1978.
3
Isolation and characterization of mutations creating high-efficiency transcription initiation signals within the trp operon of Escherichia coli.大肠杆菌色氨酸操纵子内产生高效转录起始信号的突变的分离与鉴定。
J Bacteriol. 1976 Nov;128(2):557-72. doi: 10.1128/jb.128.2.557-572.1976.
4
Mutant strains of Escherichia coli K-12 exhibiting enhanced sensitivity to 5-methyltryptophan.对5-甲基色氨酸表现出增强敏感性的大肠杆菌K-12突变菌株。
J Bacteriol. 1972 Oct;112(1):93-101. doi: 10.1128/jb.112.1.93-101.1972.
5
Restoration of phosphoribosyl transferase activity by partially deleting the trpB gene in the tryptophan operon of Salmonella typhimurium.通过部分缺失鼠伤寒沙门氏菌色氨酸操纵子中的trpB基因来恢复磷酸核糖转移酶活性。
J Bacteriol. 1972 Nov;112(2):877-85. doi: 10.1128/jb.112.2.877-885.1972.
6
Naturally occurring sites within the Shigella dysenteriae tryptophan operon severely limit tryptophan biosynthesis.痢疾志贺氏菌色氨酸操纵子内的天然存在位点严重限制色氨酸的生物合成。
J Bacteriol. 1976 May;126(2):668-78. doi: 10.1128/jb.126.2.668-678.1976.
7
Modelling the evolution of the archeal tryptophan synthase.古菌色氨酸合成酶进化的建模
BMC Evol Biol. 2007 Apr 10;7:59. doi: 10.1186/1471-2148-7-59.
8
Independent expression of the A gene of the tryptophan operon of Escherichia coli during tryptophan starvation.大肠杆菌色氨酸操纵子A基因在色氨酸饥饿期间的独立表达。
J Gen Microbiol. 1973 Jun;76(2):395-405. doi: 10.1099/00221287-76-2-395.
9
Expression of the tryptophan operon in merodiploids of Escherichia coli. II. Effects of polar mutations in the trpE gene.色氨酸操纵子在大肠杆菌部分二倍体中的表达。II. trpE基因中极性突变的影响。
Mol Gen Genet. 1974;131(3):247-61. doi: 10.1007/BF00267964.
10
Dual transcription of the tryptophan operon translocated into the early region of gamma.
Biochim Biophys Acta. 1976 May 3;432(2):199-211. doi: 10.1016/0005-2787(76)90162-3.

引用本文的文献

1
Genetic factors affecting recovery of nonpoint mutations in the region of a gene coding for ornithine transcarbamylase: involvement of both the F factor in its chromosomal state and the recA gene.影响鸟氨酸转氨甲酰酶编码基因区域中非点突变恢复的遗传因素:F 因子的染色体状态和 recA 基因的参与
Genetics. 1980 Dec;96(4):779-99. doi: 10.1093/genetics/96.4.779.
2
Arginine gene duplications in recombination proficient and deficient strains of Escherichia coli K 12.大肠杆菌K12重组 proficient和 deficient菌株中的精氨酸基因重复。 (这里 proficient和deficient不太明确准确含义,需结合专业知识进一步确定,推测可能是“ proficient( proficient可能有误,准确词或许是proficiently相关词比如efficient等之类准确表达‘有效、高效等意思’,这里按原文翻译)”是“有效、高效”,“deficient”是“缺陷、不足” ) 建议确认下proficient和deficient这两个词准确的专业意思表述,以便得到更精准译文 。整体准确译文大概是:大肠杆菌K12中具有有效重组能力和重组缺陷能力的菌株中的精氨酸基因重复 。 但还是以实际专业准确意思为准 。
Mol Gen Genet. 1974;132(3):241-53. doi: 10.1007/BF00269397.
3
Peptide transport in Salmonella typhimurium: molecular cloning and characterization of the oligopeptide permease genes.鼠伤寒沙门氏菌中的肽转运:寡肽通透酶基因的分子克隆与特性分析
Mol Gen Genet. 1987 Jan;206(1):101-9. doi: 10.1007/BF00326543.
4
Increased loss of duplicated genes in streptomycin-resistant (strA) mutants of Escherichia coli k-12.大肠杆菌K-12链霉素抗性(strA)突变体中重复基因的丢失增加。
J Bacteriol. 1976 Jan;125(1):382-4. doi: 10.1128/jb.125.1.382-384.1976.
5
Gene rearrangements in the evolution of the tryptophan synthetic pathway.色氨酸合成途径进化中的基因重排。
Bacteriol Rev. 1975 Jun;39(2):87-120. doi: 10.1128/br.39.2.87-120.1975.
6
Extrachromosomal elements as possible agents of adaptation and development.作为适应与发育潜在因子的染色体外元件
Bacteriol Rev. 1976 Sep;40(3):552-90. doi: 10.1128/br.40.3.552-590.1976.
7
Promoter-like mutants with increased expression of the Escherichia coli uridine phosphorylase structural gene.具有增加的大肠杆菌尿苷磷酸化酶结构基因表达的启动子样突变体。
J Bacteriol. 1979 Feb;137(2):802-10. doi: 10.1128/jb.137.2.802-810.1979.
8
Genetic instability in auxotrophs of Salmonella typhimurium requiring cysteine or methionine and resistant to inhibition by 1,2,4-triazole.鼠伤寒沙门氏菌营养缺陷型的遗传不稳定性,这些营养缺陷型需要半胱氨酸或甲硫氨酸,并对1,2,4-三唑的抑制具有抗性。
Genetics. 1978 Jul;89(3):419-37. doi: 10.1093/genetics/89.3.419.
9
Re-initiation of tryptophan operon expression in a promoter deletion strain of Salmonella typhimurium.鼠伤寒沙门氏菌启动子缺失菌株中色氨酸操纵子表达的重新起始
Mol Gen Genet. 1978 Jan 17;158(3):239-50. doi: 10.1007/BF00267195.
10
Genetic and segregation analysis of Escherichia coli strains containing a tandem duplication of the trpD-purB region of the chromosome.含有染色体trpD-purB区域串联重复的大肠杆菌菌株的遗传与分离分析。
J Bacteriol. 1978 Feb;133(2):650-60. doi: 10.1128/jb.133.2.650-660.1978.

本文引用的文献

1
The genetic basis of hyper-synthesis of beta-galactosidase.β-半乳糖苷酶过度合成的遗传基础。
Genetics. 1963 Feb;48(2):157-69. doi: 10.1093/genetics/48.2.157.
2
Acetylornithinase of Escherichia coli: partial purification and some properties.大肠杆菌的乙酰鸟氨酸酶:部分纯化及某些性质
J Biol Chem. 1956 Jan;218(1):97-106.
3
Polarity and enzyme functions in mutants of the first three genes of the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子前三个基因的突变体中的极性和酶功能。
Genetics. 1971 Dec;69(4):409-33. doi: 10.1093/genetics/69.4.409.
4
Duplication of the structural gene for glycyl-transfer RNA synthetase in Escherichia coli.大肠杆菌中甘氨酰 - 转移RNA合成酶结构基因的复制。
J Mol Biol. 1971 Jun 14;58(2):595-610. doi: 10.1016/0022-2836(71)90374-3.
5
Instability of a missense suppressor resulting from a duplication of genetic material.由遗传物质重复导致的错义抑制子的不稳定性。
J Mol Biol. 1969 Feb 14;39(3):563-81. doi: 10.1016/0022-2836(69)90146-6.
6
A transcription-initiating mutation within a structural gene of the tryptophan operon.色氨酸操纵子结构基因内的转录起始突变。
J Mol Biol. 1969 May 14;41(3):317-28. doi: 10.1016/0022-2836(69)90278-2.
7
The internal low-efficiency promoter of the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子的内部低效启动子。
J Mol Biol. 1968 Dec;38(3):447-51. doi: 10.1016/0022-2836(68)90401-4.
8
Internal deletions in the tryptophan operon of Escherichia coli.大肠杆菌色氨酸操纵子中的内部缺失
J Mol Biol. 1972 Nov 14;71(2):149-61. doi: 10.1016/0022-2836(72)90343-9.
9
Internal promoter of the tryptophan operon of Escherichia coli is located in a structural gene.大肠杆菌色氨酸操纵子的内部启动子位于一个结构基因中。
J Mol Biol. 1972 Aug 21;69(2):307-13. doi: 10.1016/0022-2836(72)90232-x.

大肠杆菌中色氨酸操纵子基因的重复易位

Duplication-translocations of tryptophan operon genes in Escherichia coli.

作者信息

Jackson E N, Yanofsky C

出版信息

J Bacteriol. 1973 Oct;116(1):33-40. doi: 10.1128/jb.116.1.33-40.1973.

DOI:10.1128/jb.116.1.33-40.1973
PMID:4583218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC246387/
Abstract

Mutants of Escherichia coli were selected in which a single mutational event had both relieved the polar effect of an early trpE mutation on trpB and simultaneously released the expression of trpB from tryptophan repression. The frequency at which these mutations appeared was roughly equal to the frequency of point mutations. In each of these mutants, the mutation increased the function of trpB and also increased the activity of some, but not all, of the other four tryptophan operon genes. Genetic analysis showed that the mutations were not located within the trp operon since in each case the parental trp operon could be recovered from the mutants. Each mutant was shown to carry a duplication of a trp operon segment translocated to a new position near the trp operon. Polarity is relieved since the trpB duplication-translocation is not in the same operon as the trpE polar mutation. The duplicated and translocated segments are fused to operons not regulated by tryptophan, so trpB function is no longer subject to tryptophan repression. The properties of the mutants indicate that the length of the duplicated segment and the position to which it is translocated differ in each of the seven mutants studied. The duplications are unstable, but the segregation pattern observed is not consistent with a single crossover model for segregation. That such duplication-translocation events generate a variety of new genetic arrangements at a frequency comparable with point mutations suggests they may play an important role in evolution.

摘要

挑选出了大肠杆菌的突变体,其中单个突变事件既能消除早期trpE突变对trpB的极性效应,又能同时使trpB的表达从色氨酸阻遏中释放出来。这些突变出现的频率大致与点突变的频率相等。在每一个这样的突变体中,该突变增强了trpB的功能,同时也增强了其他四个色氨酸操纵子基因中部分(而非全部)基因的活性。遗传分析表明,这些突变并不位于trp操纵子内,因为在每种情况下,亲代trp操纵子都可以从突变体中恢复。结果显示,每个突变体都携带了一个trp操纵子片段的重复,该片段易位到trp操纵子附近的一个新位置。由于trpB重复 - 易位与trpE极性突变不在同一个操纵子中,极性效应得以消除。重复并易位的片段与不受色氨酸调控的操纵子融合,因此trpB的功能不再受色氨酸阻遏。这些突变体的特性表明,在所研究的七个突变体中,每个突变体的重复片段长度及其易位的位置都有所不同。这些重复是不稳定的,但观察到的分离模式与用于分离的单交换模型不一致。这种重复 - 易位事件以与点突变相当的频率产生各种新的基因排列,这表明它们可能在进化中发挥重要作用。