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核酮糖-1,5-二磷酸羧化酶(Rubisco)而非核酮糖-1,5-二磷酸羧化酶活化酶聚集在聚球藻属蓝细菌聚球藻PCC 7942的羧酶体中:泥浆诱导的无羧酶体突变体。

Rubisco but not Rubisco activase is clustered in the carboxysomes of the cyanobacterium Synechococcus sp. PCC 7942: Mud-induced carboxysomeless mutants.

作者信息

Friedberg D, Jager K M, Kessel M, Silman N J, Bergman B

机构信息

Department of Applied Microbiology, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Mol Microbiol. 1993 Sep;9(6):1193-201. doi: 10.1111/j.1365-2958.1993.tb01248.x.

Abstract

The Mud technology of Groisman and Casadaban was adapted to the cyanobacterium Synechococcus sp. PCC 7942. A new high-CO2-requiring (hcr) mutant, hcr Mu28 was isolated following the integration of the Mud element 89 bp upstream of ORFI, at the 5'-flanking region of the rbc operon, which encodes RuBP carboxylase/oxygenase (Rubisco). The integration involved a 7 bp duplication that formed a direct repeat at the integration site, as previously shown in Escherichia coli. The mutant was devoid of apparent carboxysome bodies, which are considered to be important for the availability of CO2 for Rubisco. Immunolabelling studies demonstrated that Rubisco was distributed throughout hcr Mu28 cells, while in the wild type (WT) and in the carboxysome aberrant mutant hcr O221, Rubisco was markedly associated with the carboxysomes. Rubisco activase, however, was evenly distributed throughout the cytosol of the hcr and WT cells, without any preferential association with the apparent carboxysomes.

摘要

格罗斯曼和卡萨达班的 Mud 技术被应用于蓝藻聚球藻属 Synechococcus sp. PCC 7942。在编码核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)的 rbc 操纵子 5'侧翼区域,ORF1 上游 89 bp 处整合 Mud 元件后,分离出了一种新的高二氧化碳需求(hcr)突变体 hcr Mu28。如先前在大肠杆菌中所示,整合过程涉及在整合位点形成直接重复的 7 bp 重复序列。该突变体没有明显的羧基体,而羧基体被认为对 Rubisco 获取二氧化碳很重要。免疫标记研究表明,Rubisco 在 hcr Mu28 细胞中均匀分布,而在野生型(WT)和羧基体异常突变体 hcr O221 中,Rubisco 明显与羧基体相关。然而,Rubisco 活化酶在 hcr 和 WT 细胞的整个细胞质中均匀分布,与明显的羧基体没有任何优先关联。

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