Haferkamp Ilka, Deschamps Philippe, Ast Michelle, Jeblick Wolfgang, Maier Uwe, Ball Steven, Neuhaus H Ekkehard
Pflanzenphysiologie, Fachbereich Biologie,Technische Universität Kaiserslautern, D-67663 Kaiserslautern, Germany.
Eukaryot Cell. 2006 Jun;5(6):964-71. doi: 10.1128/EC.00381-05.
Starch in synchronously grown Guillardia theta cells accumulates throughout the light phase, followed by a linear degradation during the night. In contrast to the case for other unicellular algae such as Chlamydomonas reinhardtii, no starch turnover occurred in this organism under continuous light. The gene encoding granule-bound starch synthase (GBSS1), the enzyme responsible for amylose synthesis, displays a diurnal expression cycle. The pattern consisted of a maximal transcript abundance around the middle of the light phase and a very low level during the night. This diurnal regulation of GBSS1 transcript abundance was demonstrated to be independent of the circadian clock but tightly light regulated. A similar yet opposite type of regulation pattern was found for two alpha-amylase isoforms and for one of the two plastidic triose phosphate transporter genes investigated. In these cases, however, the transcript abundance peaked in the night phase. The second plastidic triose phosphate transporter gene had the GBSS1 mRNA abundance pattern. Quantification of the GBSS1 activity revealed that not only gene expression but also total enzyme activity exhibited a maximum in the middle of the light phase. To gain a first insight into the transport processes involved in starch biosynthesis in cryptophytes, we demonstrated the presence of both plastidic triose phosphate transporter and plastidic ATP/ADP transporter activities in proteoliposomes harboring either total membranes or plastid envelope membranes from G. theta. These molecular and biochemical data are discussed with respect to the environmental conditions experienced by G. theta and with respect to the unique subcellular location of starch in cryptophytes.
在同步生长的古列尔藻(Guillardia theta)细胞中,淀粉在整个光照阶段积累,随后在夜间呈线性降解。与莱茵衣藻(Chlamydomonas reinhardtii)等其他单细胞藻类不同,在持续光照下该生物体中未发生淀粉周转。编码颗粒结合淀粉合酶(GBSS1)的基因,即负责直链淀粉合成的酶,呈现昼夜表达周期。该模式包括在光照阶段中期转录本丰度最高,而在夜间水平极低。GBSS1转录本丰度的这种昼夜调节被证明独立于生物钟,但受光照严格调控。对于所研究的两种α-淀粉酶同工型和两种质体磷酸丙糖转运蛋白基因中的一种,发现了类似但相反的调节模式。然而,在这些情况下,转录本丰度在夜间达到峰值。第二个质体磷酸丙糖转运蛋白基因具有GBSS1 mRNA丰度模式。GBSS1活性的定量分析表明,不仅基因表达,而且总酶活性在光照阶段中期也达到最大值。为了初步了解隐藻淀粉生物合成中涉及的转运过程,我们证明了在含有古列尔藻总膜或质体包膜的蛋白脂质体中存在质体磷酸丙糖转运蛋白和质体ATP/ADP转运蛋白活性。结合古列尔藻所经历的环境条件以及隐藻中淀粉独特的亚细胞定位,对这些分子和生化数据进行了讨论。