Li Jin, Pan Hu, Yang Hui, Wang Chong, Liu Huhu, Zhou Hui, Li Peiwang, Li Changzhu, Lu Xiangyang, Tian Yun
College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, China.
Institute of Agricultural Product Quality Standard and Testing Research, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, China.
Front Microbiol. 2021 Jul 30;12:697963. doi: 10.3389/fmicb.2021.697963. eCollection 2021.
The enhancement of nitrogen fixation activity of diazotrophs is essential for safe crop production. Lysine succinylation (K) is widely present in eukaryotes and prokaryotes and regulates various biological process. However, knowledge of the extent of K in nitrogen fixation of is scarce. In this study, we found that 250 mg/l of rhamnolipid (RL) significantly increased the nitrogen fixation activity of by 39%, as compared with the control. Real-time quantitative reverse transcription PCR (qRT-PCR) confirmed that RL could remarkably increase the transcript levels of and genes. In addition, a global K of was profiled using a 4D label-free quantitative proteomic approach. In total, 5,008 K sites were identified on 1,376 succinylated proteins. Bioinformatics analysis showed that the addition of RL influence on the K level, and the succinylated proteins were involved in various metabolic processes, particularly enriched in oxidative phosphorylation, tricarboxylic acid cycle (TCA) cycle, and nitrogen metabolism. Meanwhile, multiple succinylation sites on MoFe protein (NifDK) may influence nitrogenase activity. These results would provide an experimental basis for the regulation of biological nitrogen fixation with K and shed new light on the mechanistic study of nitrogen fixation.
固氮微生物固氮活性的增强对于安全的作物生产至关重要。赖氨酸琥珀酰化(K)广泛存在于真核生物和原核生物中,并调节各种生物过程。然而,关于K在固氮过程中的作用程度的了解却很少。在本研究中,我们发现与对照相比,250 mg/l的鼠李糖脂(RL)显著提高了固氮活性39%。实时定量逆转录PCR(qRT-PCR)证实,RL可显著提高相关基因的转录水平。此外,使用4D无标记定量蛋白质组学方法对固氮微生物的整体K进行了分析。总共在1376个琥珀酰化蛋白上鉴定出5008个K位点。生物信息学分析表明,RL的添加会影响K水平,且琥珀酰化蛋白参与各种代谢过程,尤其富集于氧化磷酸化、三羧酸循环(TCA)和氮代谢。同时,钼铁蛋白(NifDK)上的多个琥珀酰化位点可能影响固氮酶活性。这些结果将为利用K调控生物固氮提供实验依据,并为固氮的机制研究提供新的线索。