Suppr超能文献

嗜热栖热放线菌中藻蓝蛋白α和β亚基基因的核苷酸序列及表达

Nucleotide sequence and expression of the genes for the alpha and beta subunits of phycocyanin in Cyanidium caldarium.

作者信息

Troxler R F, Yan Y, Jiang J W, Liu B

机构信息

Department of Biochemistry, Boston University School of Medicine, Massachusetts 02118.

出版信息

Plant Physiol. 1995 Mar;107(3):985-94. doi: 10.1104/pp.107.3.985.

Abstract

The nucleotide sequence of the plastid-encoded operon containing genes for the alpha (cpcA) and beta (cpcB) subunits of phycocyanin in the unicellular red alga Cyanidium caldarium is described. cpcB is located 5' to cpcA and the two genes are separated by a 102-bp spacer region. The transcription start site of cpcBA was mapped to 80 bp upstream of the ATG initiation codon of cpcB. Promoter-like elements similar to the -10 (TATAAT) and -35 (TTGACA) consensus promoters in bacteria were found 6 and 31 bp upstream of the transcription initiation site. Northern blotting revealed an abundant 1.3-kb cpcBA transcript in illuminated cells, but this transcript was undetectable in dark-grown cells. Expression levels of cpcBA in cells incubated with 10(-6) M heme in the dark were similar to those in cells illuminated for 24 h. Cells illuminated with 150 microM gabaculine (an inhibitor of delta-aminolevulinate synthesis) or 10 mM levulinic acid (an inhibitor of delta-aminolevulinate dehydrase) lacked detectable cpcBA transcripts. In cells illuminated with 200 microM N-methyl-mesoporphyrin IX (an inhibitor of ferrocheletase), inhibition of cpcBA expression and phycocyanin synthesis was similar. These results provide strong evidence that light induction of the cpcBA operon is dependent on synthesis of heme.

摘要

描述了单细胞红藻嗜热栖热菌中质体编码操纵子的核苷酸序列,该操纵子包含藻蓝蛋白α亚基(cpcA)和β亚基(cpcB)的基因。cpcB位于cpcA的5'端,两个基因被一个102 bp的间隔区隔开。cpcBA的转录起始位点被定位到cpcB的ATG起始密码子上游80 bp处。在转录起始位点上游6 bp和31 bp处发现了类似于细菌中-10(TATAAT)和-35(TTGACA)共有启动子的启动子样元件。Northern印迹显示,在光照细胞中有丰富的1.3 kb cpcBA转录本,但在黑暗生长的细胞中未检测到该转录本。在黑暗中用10^(-6) M血红素处理的细胞中,cpcBA的表达水平与光照24小时的细胞相似。用150 μM加巴喷丁(δ-氨基乙酰丙酸合成抑制剂)或10 mM乙酰丙酸(δ-氨基乙酰丙酸脱水酶抑制剂)处理的光照细胞缺乏可检测到的cpcBA转录本。在用200 μM N-甲基中卟啉IX(亚铁螯合酶抑制剂)处理的光照细胞中,对cpcBA表达和藻蓝蛋白合成的抑制作用相似。这些结果提供了强有力的证据,表明cpcBA操纵子的光诱导依赖于血红素的合成。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验