Department of Plant Biology, Carnegie Institution of Washington, 290 Panama Street, Stanford, CA 94305.
Proc Natl Acad Sci U S A. 1984 Oct;81(19):6049-53. doi: 10.1073/pnas.81.19.6049.
The unicellular green alga Chlamydomonas reinhardtii synthesizes carbonic anhydrase in response to low levels of CO(2) (i.e., air levels of CO(2)). This enzyme, localized predominantly in the periplasmic space of the alga (or associated with the cell wall), is an important component of the machinery required for the active accumulation of inorganic carbon by C. reinhardtii and the saturation of ribulose-1,5-bisphosphate carboxylase at low extracellular carbon concentrations. We have begun to examine the synthesis and compartmentalization of carbonic anhydrase in C. reinhardtii. The monomeric species associated with carbonic anhydrase activity is synthesized as a precursor on 80S cytoplasmic ribosomes. This precursor can be detected immunologically in the profiles of translation products when a reticulocyte lysate, cell-free system is primed with poly(A)-RNA from either air-grown C. reinhardtii or cells shifted from growth on 5% CO(2) to air for 12 hr. It is not synthesized when the in vitro system is primed with poly(A)-RNA from CO(2)-grown algae. Since translatable RNA for the polypeptide responsible for carbonic anhydrase activity was only present in cells that experienced low levels of CO(2), the adaptation process either involves the regulation of transcription of the carbonic anhydrase gene (and perhaps other genes involved in adaptation) or the post-transcriptional processing of the messenger RNA. Furthermore, the appearance of the mature polypeptide associated with carbonic anhydrase activity in the periplasmic space of C. reinhardtii is inhibited by tunicamycin, an antibiotic that prevents core glycosylation of polypeptides on the endoplasmic reticulum. Together, these results suggest that the biosynthesis of this extracellular algal enzyme involves the translation of mRNA for the carbonic anhydrase monomer on ribosomes bound to the endoplasmic reticulum, the cleavage of a signal sequence during transport of the nascent polypeptide into the lumen of the endoplasmic reticulum, and subsequent glycosylation events prior to export across the plasmalemma.
单细胞绿藻莱茵衣藻在 CO2 水平较低(即空气水平的 CO2)时合成碳酸酐酶。这种酶主要定位于藻类的周质空间(或与细胞壁相关),是 C. reinhardtii 主动积累无机碳和饱和核酮糖-1,5-二磷酸羧化酶所必需的机制的重要组成部分在低细胞外碳浓度下。我们已经开始研究 C. reinhardtii 中碳酸酐酶的合成和区室化。与碳酸酐酶活性相关的单体形式是在 80S 细胞质核糖体上作为前体合成的。当用来自空气培养的 C. reinhardtii 或从 5% CO2 生长转换为空气 12 小时的细胞的 poly(A)-RNA 启动无细胞系统时,可在翻译产物的图谱中通过免疫检测到这种前体。当体外系统用来自 CO2 生长的藻类的 poly(A)-RNA 启动时,它不会合成。由于负责碳酸酐酶活性的多肽的可翻译 RNA 仅存在于经历低 CO2 水平的细胞中,因此适应过程要么涉及碳酸酐酶基因的转录调节(和可能涉及适应的其他基因),要么涉及信使 RNA 的转录后处理。此外,碳酸酐酶活性相关成熟多肽出现在 C. reinhardtii 的周质空间中,这一现象被衣霉素抑制,衣霉素是一种抗生素,可防止内质网上多肽的核心糖基化。这些结果表明,这种细胞外藻类酶的生物合成涉及与内质网结合的核糖体上碳酸酐酶单体 mRNA 的翻译、新生多肽在进入内质网腔的运输过程中信号序列的切割,以及随后在质膜外排之前的糖基化事件。