Banh Anh Thi-Mai, Thiele Björn, Chlubek Antonia, Hombach Thomas, Kleist Einhard, Matsubara Shizue
IBG-2: Plant Sciences, Forschungszentrum Jülich, 52425, Jülich, Germany.
IBG-3: Agrosphere, Forschungszentrum Jülich, 52425, Jülich, Germany.
Plant Methods. 2022 Oct 1;18(1):114. doi: 10.1186/s13007-022-00946-3.
Living cells maintain and adjust structural and functional integrity by continual synthesis and degradation of metabolites and macromolecules. The maintenance and adjustment of thylakoid membrane involve turnover of photosynthetic pigments along with subunits of protein complexes. Quantifying their turnover is essential to understand the mechanisms of homeostasis and long-term acclimation of photosynthetic apparatus. Here we report methods combining whole-plant long-term CO labeling and liquid chromatography - mass spectrometry (LC-MS) analysis to determine the size of non-labeled population (NLP) of carotenoids and chlorophylls (Chl) in leaf pigment extracts of partially C-labeled plants.
The labeling chamber enabled parallel CO labeling of up to 15 plants of Arabidopsis thaliana with real-time environmental monitoring ([CO], light intensity, temperature, relative air humidity and pressure) and recording. No significant difference in growth or photosynthetic pigment composition was found in leaves after 7-d exposure to normal CO (~ 400 ppm) or CO in the labeling chamber, or in ambient air outside the labeling chamber (control). Following chromatographic separation of the pigments and mass peak assignment by high-resolution Fourier-transform ion cyclotron resonance MS, mass spectra of photosynthetic pigments were analyzed by triple quadrupole MS to calculate NLP. The size of NLP remaining after the 7-d CO labeling was ~ 10.3% and ~ 11.5% for all-trans- and 9-cis-β-carotene, ~ 21.9% for lutein, ~ 18.8% for Chl a and 33.6% for Chl b, highlighting non-uniform turnover of these pigments in thylakoids. Comparable results were obtained in all replicate plants of the CO labeling experiment except for three that were showing anthocyanin accumulation and growth impairment due to insufficient water supply (leading to stomatal closure and less C incorporation).
Our methods allow CO labeling and estimation of NLP for photosynthetic pigments with high reproducibility despite potential variations in [CO] between the experiments. The results indicate distinct turnover rates of carotenoids and Chls in thylakoid membrane, which can be investigated in the future by time course experiments. Since C enrichment can be measured in a range of compounds, long-term CO labeling chamber, in combination with appropriate MS methods, facilitates turnover analysis of various metabolites and macromolecules in plants on a time scale of hours to days.
活细胞通过代谢物和大分子的持续合成与降解来维持和调整结构与功能的完整性。类囊体膜的维持和调整涉及光合色素以及蛋白质复合物亚基的周转。量化它们的周转对于理解光合装置的稳态机制和长期适应性至关重要。在此,我们报告了结合整株植物长期¹⁴CO标记和液相色谱 - 质谱(LC-MS)分析来确定部分¹⁴C标记植物叶片色素提取物中类胡萝卜素和叶绿素(Chl)未标记群体(NLP)大小的方法。
标记室能够对多达15株拟南芥进行平行¹⁴CO标记,并实时监测([¹⁴CO]、光照强度、温度、相对空气湿度和压力)并记录环境数据。在正常¹⁴CO(约400 ppm)或标记室内的¹⁴CO中暴露7天,以及在标记室外的环境空气中(对照),叶片的生长或光合色素组成均未发现显著差异。通过高分辨率傅里叶变换离子回旋共振质谱对色素进行色谱分离和质量峰归属后,用三重四极杆质谱分析光合色素的质谱图以计算NLP。¹⁴CO标记7天后,全反式和9-顺式-β-胡萝卜素的NLP大小分别约为10.3%和11.5%,叶黄素约为21.9%,叶绿素a约为18.8%,叶绿素b约为33.6%,突出了类囊体中这些色素周转的不均匀性。除了三株因供水不足(导致气孔关闭和¹⁴C掺入减少)而出现花青素积累和生长受损的植株外,¹⁴CO标记实验的所有重复植株都得到了可比的结果。
尽管实验之间[¹⁴CO]可能存在差异,但我们的方法仍能实现¹⁴CO标记并以高重现性估计光合色素的NLP。结果表明类囊体膜中类胡萝卜素和叶绿素的周转速率不同,未来可通过时间进程实验进行研究。由于可以在一系列化合物中测量¹⁴C富集,长期¹⁴CO标记室与适当的质谱方法相结合,有助于在数小时至数天的时间尺度上分析植物中各种代谢物和大分子的周转。