首页> 外文期刊>Plant Physiology >Thylakoid Lumen Carbonic Anhydrase (CAH3) Mutation Suppresses Air-Dier Phenotype of LCIB Mutant in Chlamydomonas reinhardtii1,[C],[OA]
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Thylakoid Lumen Carbonic Anhydrase (CAH3) Mutation Suppresses Air-Dier Phenotype of LCIB Mutant in Chlamydomonas reinhardtii1,[C],[OA]

机译:类囊体腔碳酸酐酶(CAH3)突变抑制莱茵衣藻LCIB突变体的空表型[C],[OA]

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摘要

An active CO2-concentrating mechanism is induced when Chlamydomonas reinhardtii acclimates to limiting inorganic carbon (Ci), either low-CO2 (L-CO2; air level; approximately 0.04% CO2) or very low-CO2 (VL-CO2; approximately 0.01% CO2) conditions. A mutant, ad1, which is defective in the limiting-CO2-inducible, plastid-localized LCIB, can grow in high-CO2 or VL-CO2 conditions but dies in L-CO2, indicating a deficiency in a L-CO2-specific Ci uptake and accumulation system. In this study, we identified two ad1 suppressors that can grow in L-CO2 but die in VL-CO2. Molecular analyses revealed that both suppressors have mutations in the CAH3 gene, which encodes a thylakoid lumen localized carbonic anhydrase. Photosynthetic rates of L-CO2-acclimated suppressors under acclimation CO2 concentrations were more than 2-fold higher than ad1, apparently resulting from a more than 20-fold increase in the intracellular concentration of Ci as measured by direct Ci uptake. However, photosynthetic rates of VL-CO2-acclimated cells under acclimation CO2 concentrations were too low to support growth in spite of a significantly elevated intracellular Ci concentration. We conclude that LCIB functions downstream of CAH3 in the CO2-concentrating mechanism and probably plays a role in trapping CO2 released by CAH3 dehydration of accumulated Ci. Apparently dehydration by the chloroplast stromal carbonic anhydrase CAH6 of the very high internal Ci caused by the defect in CAH3 provides Rubisco sufficient CO2 to support growth in L-CO2-acclimated cells, but not in VL-CO2-acclimated cells, even in the absence of LCIB.
机译:当莱茵衣藻适应有限的无机碳(Ci)时,诱导了活跃的CO2浓缩机制,即低CO2(L-CO2;空气水平;约0.04%CO2)或非常低的CO2(VL-CO2;约0.01%)。 CO2)条件。在限制性CO2诱导的质体定位LCIB中有缺陷的突变体ad1可以在高CO2或VL-CO2条件下生长,但在L-CO2中死亡,表明L-CO2特异性Ci缺乏吸收和积累系统。在这项研究中,我们确定了两种ad1抑制剂,它们可以在L-CO2中生长但在VL-CO2中死亡。分子分析表明,两种抑制剂在CAH3基因中都有突变,该基因编码类囊体腔定位的碳酸酐酶。在适应CO2浓度的条件下,适应L-CO2的抑制剂的光合速率比ad1高2倍以上,这显然是由于直接摄取Ci所测量的胞内Ci浓度增加了20倍以上。然而,尽管细胞内Ci浓度显着升高,但在适应CO2浓度下,适应VL-CO2的细胞的光合速率仍然过低,无法支持生长。我们得出的结论是,LCIB在CO2浓缩机制中在CAH3的下游起作用,并可能在捕集CAH3脱水积累的Ci释放的CO2时起作用。由CAH3缺陷引起的非常高的内部Ci的叶绿体间质碳酸酐酶CAH6显然提供了Rubisco足够的CO2来支持L-CO2适应的细胞的生长,但在VL-CO2适应的细胞中却没有,即使没有LCIB。

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