MSU-DOE Plant Research Laboratory and Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824, U.S.A.
Plant Resilience Institute, Michigan State University, East Lansing, MI 48824, U.S.A.
Biochem J. 2020 Sep 18;477(17):3237-3252. doi: 10.1042/BCJ20200480.
Feeding 14CO2 was crucial to uncovering the path of carbon in photosynthesis. Feeding 13CO2 to photosynthesizing leaves emitting isoprene has been used to develop hypotheses about the sources of carbon for the methylerythritol 4-phosphate pathway, which makes the precursors for terpene synthesis in chloroplasts and bacteria. Both photosynthesis and isoprene studies found that products label very quickly (<10 min) up to 80-90% but the last 10-20% of labeling requires hours indicating a source of 12C during photosynthesis and isoprene emission. Furthermore, studies with isoprene showed that the proportion of slow label could vary significantly. This was interpreted as a variable contribution of carbon from sources other than the Calvin-Benson cycle (CBC) feeding the methylerythritol 4-phosphate pathway. Here, we measured the degree of label in isoprene and photosynthetic metabolites 20 min after beginning to feed 13CO2. Isoprene labeling was the same as labeling of photosynthesis intermediates. High temperature reduced the label in isoprene and photosynthesis intermediates by the same amount indicating no role for alternative carbon sources for isoprene. A model assuming glucose, fructose, and/or sucrose reenters the CBC as ribulose 5-phosphate through a cytosolic shunt involving glucose 6-phosphate dehydrogenase was consistent with the observations.
给正在进行光合作用的叶子投喂 13CO2 以供其释放异戊二烯,这一方法被用于提出关于甲基赤藓醇 4-磷酸途径碳源的假说,该途径为质体和细菌中的萜烯合成提供前体。光合作用和异戊二烯研究都发现,产物的标记速度非常快(<10min),可达到 80-90%,但最后 10-20%的标记需要数小时,这表明在光合作用和异戊二烯排放过程中有 12C 的来源。此外,异戊二烯的研究表明,慢标记的比例可能有很大差异。这被解释为来自卡尔文-本森循环(CBC)以外的碳源对甲基赤藓醇 4-磷酸途径的可变贡献。在这里,我们测量了在开始投喂 13CO2 20 分钟后异戊二烯和光合作用代谢物中的标记程度。异戊二烯的标记与光合作用中间体的标记相同。高温使异戊二烯和光合作用中间体中的标记减少了相同的量,这表明异戊二烯没有替代碳源。一个假设葡萄糖、果糖和/或蔗糖通过涉及葡萄糖 6-磷酸脱氢酶的细胞质分流重新进入 CBC 作为核酮糖 5-磷酸的模型与观察结果一致。