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哈氏弧菌和费氏弧菌的荧光素酶在丝状蓝细菌中的表达

Expression of luciferases from Vibrio harveyi and Vibrio fischeri in filamentous cyanobacteria.

作者信息

Schmetterer G, Wolk C P, Elhai J

出版信息

J Bacteriol. 1986 Jul;167(1):411-4. doi: 10.1128/jb.167.1.411-414.1986.

DOI:10.1128/jb.167.1.411-414.1986
PMID:3087964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC212896/
Abstract

Shuttle vectors that had previously been shown to replicate both in Escherichia coli and in strains of Anabaena spp. were used to transfer the lux genes from Vibrio harveyi and Vibrio fischeri into Anabaena spp. The level of expression of luciferase in the cyanobacteria (up to 7,000 quanta cell-1 s-1) makes these genes good candidates for use as promoter probes during the differentiation of certain cells in a filament into heterocysts.

摘要

先前已证明能在大肠杆菌和鱼腥藻属菌株中复制的穿梭载体,被用于将哈维氏弧菌和费氏弧菌的荧光素酶基因转移到鱼腥藻属中。蓝细菌中荧光素酶的表达水平(高达7000光量子·细胞⁻¹·秒⁻¹)使得这些基因成为丝状藻丝中某些细胞分化为异形胞过程中用作启动子探针的良好候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be3f/212896/dca24b248fc2/jbacter00206-0423-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be3f/212896/dca24b248fc2/jbacter00206-0423-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be3f/212896/dca24b248fc2/jbacter00206-0423-a.jpg

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本文引用的文献

1
Isolation and sequence of the gene for the large subunit of ribulose-1,5-bisphosphate carboxylase from the cyanobacterium Anabaena 7120.从蓝藻鱼腥藻 7120 中分离并测定核酮糖-1,5-二磷酸羧化酶大亚基的基因序列。
Proc Natl Acad Sci U S A. 1983 Apr;80(7):1835-9. doi: 10.1073/pnas.80.7.1835.
2
Nucleotide sequence of a cyanobacterial nifH gene coding for nitrogenase reductase.蓝细菌 nifH 基因编码氮酶还原酶的核苷酸序列。
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6476-80. doi: 10.1073/pnas.77.11.6476.
3
Bacterial bioluminescence: isolation and expression of the luciferase genes from Vibrio harveyi.
用于革兰氏阳性菌的新型基于盒式的穿梭载体系统。
Appl Environ Microbiol. 2004 Oct;70(10):6076-85. doi: 10.1128/AEM.70.10.6076-6085.2004.
4
Use of bacterial luciferase to establish a promoter probe vehicle capable of nondestructive real-time analysis of gene expression in Bacillus spp.利用细菌荧光素酶构建一种启动子探针载体,用于对芽孢杆菌属基因表达进行无损实时分析。
J Bacteriol. 1987 May;169(5):2165-70. doi: 10.1128/jb.169.5.2165-2170.1987.
5
The use of the luxA gene of the bacterial luciferase operon as a reporter gene.
Mol Gen Genet. 1988 Dec;215(1):1-9. doi: 10.1007/BF00331295.
6
Expression of the Caulobacter heat shock gene dnaK is developmentally controlled during growth at normal temperatures.柄杆菌热休克基因dnaK的表达在正常温度下生长期间受到发育调控。
J Bacteriol. 1990 Jun;172(6):3051-9. doi: 10.1128/jb.172.6.3051-3059.1990.
7
Developmental regulation and spatial pattern of expression of the structural genes for nitrogenase in the cyanobacterium Anabaena.蓝藻鱼腥藻中固氮酶结构基因的表达发育调控及空间模式
EMBO J. 1990 Oct;9(10):3379-88. doi: 10.1002/j.1460-2075.1990.tb07539.x.
8
Characterization of cryptic plasmids from marine cyanobacteria and construction of a hybrid plasmid potentially capable of transformation of marine cyanobacterium, Synechococcus sp., and its transformation.海洋蓝藻中隐蔽质粒的特性分析以及构建一种可能能够转化海洋蓝藻聚球藻属(Synechococcus sp.)的杂种质粒及其转化
Appl Biochem Biotechnol. 1990 Spring-Summer;24-25:151-60. doi: 10.1007/BF02920241.
9
Identification and characterization of hetA, a gene that acts early in the process of morphological differentiation of heterocysts.异形胞形态分化过程早期起作用的基因hetA的鉴定与特性分析。
J Bacteriol. 1990 Jun;172(6):3131-7. doi: 10.1128/jb.172.6.3131-3137.1990.
10
Molecular biology of bacterial bioluminescence.细菌生物发光的分子生物学
Microbiol Rev. 1991 Mar;55(1):123-42. doi: 10.1128/mr.55.1.123-142.1991.
细菌生物发光:哈维弧菌荧光素酶基因的分离与表达
Science. 1982 Nov 19;218(4574):791-3. doi: 10.1126/science.10636771.
4
A rapid whole-cell assay for superoxide dismutase.
Anal Biochem. 1982 Mar 15;121(1):207-12. doi: 10.1016/0003-2697(82)90577-2.
5
Bacterial bioluminescence: isolation and genetic analysis of functions from Vibrio fischeri.细菌生物发光:费氏弧菌功能的分离与遗传分析
Cell. 1983 Mar;32(3):773-81. doi: 10.1016/0092-8674(83)90063-6.
6
Construction of shuttle vectors capable of conjugative transfer from Escherichia coli to nitrogen-fixing filamentous cyanobacteria.构建能够从大肠杆菌接合转移至固氮丝状蓝细菌的穿梭载体。
Proc Natl Acad Sci U S A. 1984 Mar;81(5):1561-5. doi: 10.1073/pnas.81.5.1561.
7
Nucleotide sequence and exact localization of the neomycin phosphotransferase gene from transposon Tn5.转座子Tn5中新霉素磷酸转移酶基因的核苷酸序列及精确定位。
Gene. 1982 Oct;19(3):327-36. doi: 10.1016/0378-1119(82)90023-3.
8
A physical map of plasmid pDU1 from the cyanobacterium Nostoc PCC 7524.
Plasmid. 1982 Jan;7(1):101-4. doi: 10.1016/0147-619x(82)90032-4.
9
The plasmid cloning vector pBR325 contains a 482 base-pair-long inverted duplication.质粒克隆载体pBR325含有一段长度为482个碱基对的反向重复序列。
Gene. 1981 Sep;14(4):289-99. doi: 10.1016/0378-1119(81)90161-x.
10
New Anabaena and Nostoc cyanophages from sewage settling ponds.来自污水沉淀池的新型鱼腥藻和念珠藻噬菌体。
Virology. 1981 Oct 15;114(1):236-46. doi: 10.1016/0042-6822(81)90269-5.