1.
Roles of nitric oxide in heavy metal stress in plants: Cross-talk with phytohormones and protein S-nitrosylation.
Wei, L, Zhang, M, Wei, S, Zhang, J, Wang, C, Liao, W
Environmental pollution (Barking, Essex : 1987). 2020;:113943
Abstract
Heavy metal (HM) stress is a major hazard, which significantly affects plant growth and development. In order to confront HM stress, plants directly or indirectly regulate the levels of endogenous nitric oxide (NO), a redox-related signaling molecule involved in wide range of plant growth and development as well as in response to HM stress. In addition, there is now compelling experimental evidence that NO usually mediates signaling processes through interactions with different biomolecules like phytohormones to regulate HM tolerance. Apart from phytohormones, NO partly operates through posttranslational modification of proteins, notably via S-nitrosylation in response to HM stress. Recently, the roles of S-nitrosylation as a regulator of plant responses to HM stress and S-nitrosylated candidates have also been established and detected. Here, we describe the roles of NO in confronting HM phytotoxicity in plants with a particular focus on the presentation and discussion of recent data obtained in this field, which involves in the function of various phytohormones and S-nitrosylation during plant responses to HM stress. Additionally, both importance and challenges of future work are outlined in order to further elucidate the specific mechanisms underlying the roles of NO in plant responses to HM stress.
2.
Physiological characteristics and metabolomics of transgenic wheat containing the maize C4 phosphoenolpyruvate carboxylase (PEPC) gene under high temperature stress.
Qi, X, Xu, W, Zhang, J, Guo, R, Zhao, M, Hu, L, Wang, H, Dong, H, Li, Y
Protoplasma. 2017;(2):1017-1030
Abstract
In this paper, two transgenic wheat lines, PC27 and PC51, containing the maize PEPC gene and its wild-type (WT) were used as experimental material to study the effects of high temperature on their photosynthetic physiological characteristics and metabolome. The results showed that transgenic wheat lines had higher photosynthetic rate (P n) than WT under non-stress treatment (NT) and high temperature stress treatment (HT), and more significantly under HT. The change trends of F v/F m, ะค PSII, and q P were similar to P n, whereas that of non-photochemical quenching (NPQ) was the opposite. Compared with WT, no differences in chlorophyll content between the transgenic wheat and WT were observed under NT, but two transgenic lines had relatively higher contents than WT under HT. The change trends of Chlorophyll a/b radio, the decreased values of F m, Wk, and Vj, and the activity of the antioxidant enzyme were consistent with the chlorophyll content. Compared with WT, transgenic wheat lines exhibited lower rate of superoxide anion production, H2O2 and malondialdehyde content under HT, and no significant differences were observed under NT. The expression pattern of the ZmPEPC gene and wheat endogenous photosynthesis-related genes were in agreement with that of P n. Compared with WT, about 13 different metabolites including one organic acid, six amino acids, four sugars, and two polyols were identified under NT; 25 different metabolites including six organic acids, 12 amino acids, four sugars, and three polyols were identified under HT. Collectively, our results indicate that ZmPEPC gene can enhance photochemical and antioxidant enzyme activity, upregulate the expression of photosynthesis-related genes, delay degradation of chlorophyll, change contents of proline and other metabolites in wheat, and ultimately improves its heat tolerance.
3.
Enhancing Butanol Production under the Stress Environments of Co-Culturing Clostridium acetobutylicum/Saccharomyces cerevisiae Integrated with Exogenous Butyrate Addition.
Luo, H, Ge, L, Zhang, J, Zhao, Y, Ding, J, Li, Z, He, Z, Chen, R, Shi, Z
PloS one. 2015;(10):e0141160
Abstract
In this study, an efficient acetone-butanol-ethanol (ABE) fermentation strategy integrating Clostridium acetobutylicum/Saccharomyces cerevisiae co-culturing system with exogenous butyrate addition, was proposed and experimentally conducted. In solventogenic phase, by adding 0.2 g-DCW/L-broth viable S. cerevisiae cells and 4.0 g/L-broth concentrated butyrate solution into C. acetobutylicum culture broth, final butanol concentration and butanol/acetone ratio in a 7 L anaerobic fermentor reached the highest levels of 15.74 g/L and 2.83 respectively, with the increments of 35% and 43% as compared with those of control. Theoretical and experimental analysis revealed that, the proposed strategy could, 1) extensively induce secretion of amino acids particularly lysine, which are favorable for both C. acetobutylicum survival and butanol synthesis under high butanol concentration environment; 2) enhance the utilization ability of C. acetobutylicum on glucose and over-produce intracellular NADH for butanol synthesis in C. acetobutylicum metabolism simultaneously; 3) direct most of extra consumed glucose into butanol synthesis route. The synergetic actions of effective amino acids assimilation, high rates of substrate consumption and NADH regeneration yielded highest butanol concentration and butanol ratio in C. acetobutylicum under this stress environment. The proposed method supplies an alternative way to improve ABE fermentation performance by traditional fermentation technology.