Department of Molecular and Cell Biology, The Pennsylvania State University, University Park, Pennsylvania 16802.
Plant Physiol. 1992 Mar;98(3):1003-10. doi: 10.1104/pp.98.3.1003.
The cyanobacterium Agmenellum quadruplicatum PR-6 (Synechococcus sp PCC 7002) was grown turbidostatically in white light at three levels of irradiance: 20, 200, and 1260 microeinsteins per square meter per second. Phycobilisomes were isolated from each culture and analyzed by absorbance, gel electrophoresis, and electron microscopy. The ratio of phycocyanin to allophycocyanin decreased 1.8-fold from the lowest to highest irradiance. This change was due entirely to an approximately 2.5-fold decrease in one structural unit of rod domains, the complex of phycocyanin, and a 33-kilodalton linker polypeptide (LR33). For a given irradiance, phycobilisomes from cells grown on ammonium as the nitrogen source had 10 to 20% more phycocyanin than those from nitrate cultures. Total RNA was isolated from all cultures and probed with gene fragments specific to phycocyanin and allophycocyanin subunits and LR33. The relative level of RNAs encoding phycocyanin and allophycocyanin was found to vary with light intensity in parallel with the phycobiliprotein ratio. Hence, the light-harvesting capacity of phycobilisomes is directly regulated by relative levels of phycobiliprotein mRNA. The LR33 transcript occurs as a 3' extension on about 10% of phycocyanin transcripts. The ratio of RNA encoding LR33 to that encoding phycocyanin did not vary with irradiance, although the protein ratio changed 1.7- to twofold between extremes. Based on these and other observations, we propose that the LR33 protein is constitutively synthesized at a rate higher than that required to complex with available phycocyanin.
集胞藻 PR-6(聚球藻 PCC 7002)在白光下以三个光照水平浊度培养:20、200 和 1260 微爱因斯坦/平方米/秒。从每个培养物中分离出藻胆体,并通过吸收、凝胶电泳和电子显微镜进行分析。藻蓝蛋白与别藻蓝蛋白的比例从最低光照到最高光照降低了 1.8 倍。这种变化完全是由于杆状结构单元的一个结构单元,藻蓝蛋白和 33 千道尔顿连接多肽(LR33)的大约 2.5 倍减少。对于给定的光照,以铵作为氮源生长的细胞的藻胆体比硝酸盐培养物的藻胆体多 10%到 20%。从所有培养物中分离总 RNA,并与藻蓝蛋白和别藻蓝蛋白亚基和 LR33 的基因片段进行探针杂交。发现编码藻蓝蛋白和别藻蓝蛋白的 RNA 的相对水平与光强度平行变化,与藻胆蛋白的比例一致。因此,藻胆体的光收集能力直接受藻胆蛋白 mRNA 的相对水平调节。LR33 转录本作为藻蓝蛋白转录本的 3'延伸约占 10%。编码 LR33 的 RNA 与编码藻蓝蛋白的 RNA 的比例不因光照而变化,尽管在极端情况下,蛋白质比例变化了 1.7-到两倍。基于这些和其他观察结果,我们提出 LR33 蛋白以高于与可用藻蓝蛋白结合所需的速度持续合成。