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cpcE和cpcF突变体产生的藻蓝蛋白的特性以及胆色素附着缺陷的基因间抑制子的鉴定。

Characterization of phycocyanin produced by cpcE and cpcF mutants and identification of an intergenic suppressor of the defect in bilin attachment.

作者信息

Swanson R V, Zhou J, Leary J A, Williams T, de Lorimier R, Bryant D A, Glazer A N

机构信息

Division of Biochemistry and Molecular Biology, University of California, Berkeley 94720.

出版信息

J Biol Chem. 1992 Aug 15;267(23):16146-54.

PMID:1644802
Abstract

Mutants of the cyanobacterium Synechococcus sp. PCC 7002 constructed by the insertional inactivation of either the cpcE or cpcF gene produce low levels of spectroscopically detectable phycocyanin. The majority of the phycocyanin produced in these strains appears to lack the alpha subunit phycocyanobilin (PCB) chromophore (Zhou, J., Gasparich, G. E., Stirewalt, V. L., de Lorimier, R., and Bryant, D. A. (1992) J. Biol. Chem. 267, 16138-16145). Purification of the phycocyanin produced in the mutants revealed two fractions each with an aberrant absorption spectrum. Tryptic peptide maps of the major fraction showed that the alpha-84 PCB peptide was absent. The two PCB peptides derived from the beta subunit were normal. Tryptic digests of the less abundant phycocyanin fraction contained a family of bilin peptides derived from the alpha subunit. Several distinct bilin adducts were present. A major component was a mesobiliverdin adduct, a previously described product of the in vitro reaction of PCB and apophycocyanin. The same results were obtained with both the cpcE mutant and the cpcF mutant. In vitro reactions with PCB and the fractions containing apo alpha subunit showed that the alpha-84 bilin attachment site was unmodified and competent for adduct formation. Pseudo-revertants of both strains were observed to arise at high frequency. Analysis of the phycocyanin from a cpcE pseudo-revertant, which produced a near wild-type level of phycocyanin with alpha subunit carrying PCB, revealed a single amino acid substitution, alpha-Tyr129----Cys. This residue, which is conserved in all phycocyanins sequenced to date, forms part of the alpha-84 bilin binding site and lies within 5 A of alpha-Cys84. A mutated cpcA gene containing this substitution was constructed by site-directed mutagenesis and transformed, along with cpcB, into a cpcBAC deletion strain containing an insertionally inactivated cpcE. This strain produces high levels of phycocyanin and the majority of the alpha subunit carries PCB at alpha-Cys84.

摘要

通过插入失活cpcE或cpcF基因构建的蓝藻聚球藻属Synechococcus sp. PCC 7002突变体产生的藻蓝蛋白水平较低,通过光谱检测可检测到。这些菌株中产生的大多数藻蓝蛋白似乎缺乏α亚基藻蓝胆素(PCB)发色团(周,J.,加斯帕里奇,G.E.,斯蒂勒沃尔特,V.L.,德洛里米尔,R.,和布莱恩特,D.A.(1992)《生物化学杂志》267,16138 - 16145)。对突变体中产生的藻蓝蛋白进行纯化,发现有两个组分,每个组分的吸收光谱都异常。主要组分的胰蛋白酶肽图谱显示,α - 84 PCB肽缺失。来自β亚基的两种PCB肽是正常的。较少量藻蓝蛋白组分的胰蛋白酶消化产物含有一系列源自α亚基的胆素肽。存在几种不同的胆素加合物。主要成分是中胆绿素加合物,这是先前描述的PCB与脱辅基藻蓝蛋白体外反应的产物。cpcE突变体和cpcF突变体都得到了相同的结果。用PCB与含有脱辅基α亚基的组分进行体外反应表明,α - 84胆素连接位点未被修饰,能够形成加合物。观察到这两种菌株都以高频率出现假回复体。对来自cpcE假回复体的藻蓝蛋白进行分析,该假回复体产生的藻蓝蛋白水平接近野生型,且α亚基携带PCB,结果显示有一个氨基酸取代,α - Tyr129→Cys。这个残基在迄今为止测序的所有藻蓝蛋白中都是保守的,它构成了α - 84胆素结合位点的一部分,且位于α - Cys84的5埃范围内。通过定点诱变构建了包含此取代的突变cpcA基因,并与cpcB一起转化到一个含有插入失活cpcE的cpcBAC缺失菌株中。该菌株产生高水平的藻蓝蛋白,且大多数α亚基在α - Cys84处携带PCB。

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