Chen Jing, Chen Yuanhao, He Weiling, Liang Honghao, Hong Ting, Li Tangcheng, Du Hong
Guangdong Provincial Key Laboratory of Marine Biotechnology, STU-UNIVPM Joint Algal Research Center, Institute of Marine Sciences, Shantou University, Shantou, Guangdong, China.
Southern Marine Science and Engineering Guangdong Laboratory, Guangzhou, Guangdong, China.
Front Plant Sci. 2024 Jun 19;15:1407915. doi: 10.3389/fpls.2024.1407915. eCollection 2024.
The green alga can grow photoautotrophically utilizing light and CO, and heterotrophically utilizing acetate. The physiological and biochemical responses of autotrophy and heterotrophy are different in . However, there is no complete understanding of the molecular physiology between autotrophy and heterotrophy. Therefore, we performed biochemical, molecular and transcriptome analysis of between autotrophy and heterotrophy.
The cell growth characterization demonstrated that heterotrophic cell had enhanced growth rates, and autotrophic cell accumulated more chlorophyll. The transcriptome data showed that a total of 2,970 differentially expressed genes (DEGs) were identified from photoautotrophy 12h (P12h) to heterotrophy 12h (H12h). The DEGs were involved in photosynthesis, the tricarboxylic acid cycle (TCA), pyruvate and oxidative phosphorylation metabolisms. Moreover, the results of qRT-PCR revealed that the relative expression levels of malate dehydrogenase (MDH), succinate dehydrogenase (SDH), ATP synthase (ATPase), and starch synthase (SSS) were increased significantly from P12h and H12h. The protein activity of NAD-malate dehydrogenase (NAD-MDH) and succinate dehydrogenase (SDH) were significantly higher in the H12h group.
The above results indicated that the high growth rate observed in heterotrophic cell may be the effects of environmental or genetic regulation of photosynthesis. Therefore, the identification of novel candidate genes in heterotrophy will contribute to the development of microalga strains with higher growth capacity and better performance for biomass production.
绿藻能够利用光和二氧化碳进行光合自养生长,也能利用乙酸盐进行异养生长。在绿藻中,自养和异养的生理生化反应有所不同。然而,对于自养和异养之间的分子生理学,目前还没有完全了解。因此,我们对绿藻自养和异养进行了生化、分子和转录组分析。
细胞生长特性表明,异养细胞具有更高的生长速率,而自养细胞积累了更多的叶绿素。转录组数据显示,从光合自养12小时(P12h)到异养12小时(H12h),共鉴定出2970个差异表达基因(DEGs)。这些差异表达基因参与光合作用、三羧酸循环(TCA)、丙酮酸和氧化磷酸化代谢。此外,qRT-PCR结果显示,从P12h到H12h,苹果酸脱氢酶(MDH)、琥珀酸脱氢酶(SDH)、ATP合酶(ATPase)和淀粉合酶(SSS)的相对表达水平显著增加。在H12h组中,NAD-苹果酸脱氢酶(NAD-MDH)和琥珀酸脱氢酶(SDH)的蛋白活性显著更高。
上述结果表明,异养细胞中观察到的高生长速率可能是光合作用的环境或基因调控的结果。因此,鉴定异养中的新候选基因将有助于开发具有更高生长能力和更好生物质生产性能的微藻菌株。