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球形红杆菌捕光B800 - 850-α和B800 - 850-β基因的克隆、DNA序列及表达

Cloning, DNA sequence, and expression of the Rhodobacter sphaeroides light-harvesting B800-850-alpha and B800-850-beta genes.

作者信息

Kiley P J, Kaplan S

出版信息

J Bacteriol. 1987 Jul;169(7):3268-75. doi: 10.1128/jb.169.7.3268-3275.1987.

Abstract

Two deoxyoligonucleotide probes were synthesized in accordance with the available amino acid sequence of the B800-850-beta polypeptide from Rhodobacter sphaeroides and were used to isolate a 2.6-kilobase PstI fragment from R. sphaeroides 2.4.1 chromosomal DNA. Identification of the B800-850-beta and B800-850-alpha structural genes, pucB and pucA, was confirmed by DNA sequencing. Northern (RNA) blot analysis, using restriction endonuclease fragments from the cloned genes as probes, revealed a single puc-operon-specific, highly stable transcript of approximately 640 bases present in photosynthetically grown cells. In vitro transcription-translation analysis of the puc operon revealed that the maximum synthesis of the puc operon gene products was achieved when the entire 2.6-kilobase PstI fragment was used as the template, although a 537-base-pair XmaIII fragment was sufficient to direct the synthesis of pucB and pucA fusion product.

摘要

根据球形红细菌B800 - 850-β多肽的可用氨基酸序列合成了两种脱氧寡核苷酸探针,并用于从球形红细菌2.4.1染色体DNA中分离出一个2.6千碱基的PstI片段。通过DNA测序证实了B800 - 850-β和B800 - 850-α结构基因pucB和pucA的鉴定。使用来自克隆基因的限制性内切酶片段作为探针进行的Northern(RNA)印迹分析显示,在光合生长的细胞中存在一个约640个碱基的单一puc操纵子特异性、高度稳定的转录本。对puc操纵子的体外转录-翻译分析表明,当使用整个2.6千碱基的PstI片段作为模板时,puc操纵子基因产物的合成量最大,尽管一个537碱基对的XmaIII片段足以指导pucB和pucA融合产物的合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3dd/212379/a97814c06353/jbacter00197-0370-a.jpg

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