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Structure and regulation of genes encoding phycocyanin and allophycocyanin from Anabaena variabilis ATCC 29413.

机译:变异鱼腥藻ATCC 29413中编码藻蓝蛋白和别藻蓝蛋白的基因的结构和调控。

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摘要

Gene clones encoding phycocyanin and allophycocyanin were isolated from an Anabaena variabilis ATCC 29413-Charon 30 library by using the phycocyanin (cpc) genes of Agmenellum quadruplicatum and the allophycocyanin (apc) genes of Cyanophora paradoxa as heterologous probes. The A. variabilis cpcA and cpcB genes occur together in the genome, as do the apcA and apcB genes; the two sets of genes are not closely linked, however. The cpc and apc genes appear to be present in only one copy per genome. DNA-RNA hybridization analysis showed that expression of the cpc and apc genes is greatly decreased during nitrogen starvation; within 1 h no cpc or apc mRNA could be detected. The source of nitrogen for growth did not influence expression of the genes; vegetative cells from nitrogen-fixing and ammonia-grown cultures had approximately the same levels of cpc and apc mRNAs. Heterocysts had less than 5% as much cpc mRNA as vegetative cells from nitrogen-fixing cultures. Northern hybridization (RNA blot) analysis showed that the cpc genes are transcribed to give an abundant 1.4-kilobase (kb) RNA as well as two less prominent 3.8- and 2.6-kb species. The apc genes gave rise to two transcripts, a 1.4-kb predominant RNA and a minor 1.75-kb form.
机译:通过使用四倍体Agmenellum quadruplicatum的藻蓝蛋白(cpc)基因和Cyanophora paradoxa的藻蓝蛋白(apc)基因作为异源探针,从Anabaena variabilis ATCC 29413-Charon 30文库中分离出编码藻蓝蛋白和别藻蓝蛋白的基因克隆。变异曲霉的cpcA和cpcB基因在基因组中同时出现,apcA和apcB基因也是如此。但是,这两组基因并没有紧密联系。每个基因组中的cpc和apc基因似乎只存在一个拷贝。 DNA-RNA杂交分析表明,在氮饥饿期间,cpc和apc基因的表达大大降低。 1小时内未检测到cpc或apc mRNA。生长所需的氮源不影响基因的表达。来自固氮培养和氨生长培养的营养细胞的cpc和apc mRNA含量大致相同。与来自固氮培养物的营养细胞相比,异质囊的cpc mRNA少于5%。 Northern杂交(RNA印迹)分析表明,转录了cpc基因可提供丰富的1.4千碱基(kb)RNA以及两个不太显眼的3.8和2.6 KB物种。 apc基因产生两个转录本,一个是1.4 kb的优势RNA,另一个是1.75 kb的次要形式。

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