The enzyme myo-inositol-1-phosphate synthase(MIPS EC 5.5.1.4) catalyzes the first step of myo-inositol biosynthesis, a product that plays crucial roles in plants as an osmoprotectant, transduction molecule, cell wal...The enzyme myo-inositol-1-phosphate synthase(MIPS EC 5.5.1.4) catalyzes the first step of myo-inositol biosynthesis, a product that plays crucial roles in plants as an osmoprotectant, transduction molecule, cell wall constituent and production of stress related molecule. Previous reports highlighted an important role of MIPS family genes in abiotic stresses particularly under salt stress tolerance in several plant species; however, little is known about the cellular and physiological functions of MIPS2 genes under abiotic conditions. In this study, a novel salt stress responsive gene designated Gs MIPS2 from wild soybean Glycine soja 07256 was functionally characterized contained an open reading frame(ORF) of 1 533 bp coding a peptide sequence of 510 amino acids along with mass of 56 445 ku. Multiple sequence alignment analysis revealed its 92%-99% similarity with other MIPS family members in legume proteins. Quantitative real-time PCR results demonstrated that Gs MIPS2 was induced by salt stress and expressed in roots of soybean. The positive function of Gs MIPS2 under salt response at different growth stages of transgenic Arabidopsis was also elucidated. The results showed that Gs MIPS2 transgenic lines displayed increased tolerance as compared to WT and atmips2 mutant lines under salt stress. Furthermore, the expression levels of some salt stress responsive marker genes, including KIN1, RD29 A, RD29 B, P5 Cs and COR47 were significantly up-regulated in Gs MIPS2 overexpression lines than wild type and atmips2 mutant. Collectively, these results suggested that Gs MIPS2 gene was a positive regulator of plant tolerance to salt stress. This was the first report to demonstrate that overexpression of Gs MIPS2 gene from wild soybean improved salt tolerance in transgenic Arabidopsis.展开更多
Glycine functionalized activated carbon adsorption material(NOPAC-GLY-X)was successfully prepared by one-step thermal decomposition using agricultural waste navel orange peel as a precursor.Through batch adsorption ex...Glycine functionalized activated carbon adsorption material(NOPAC-GLY-X)was successfully prepared by one-step thermal decomposition using agricultural waste navel orange peel as a precursor.Through batch adsorption experiments,it is found that the adsorption performance of Gd(Ⅲ)on activated carbon can be significantly enhanced by glycine modification.The adsorption isotherms of the NOPACs conform to the Langmuir isotherm model,and the maximum adsorption capacity of the activated carbon sample NOPAC-Gly-60 is approximately 48.5 mg/g.The Gd(Ⅲ)adsorption capacity of navel orange peel activated carbon can be doubled after glycine modification,and the adsorption efficiency of gadolinium can reach99%at pH=7.The physicochemical properties of the prepared adsorbents were characterized by Brunauer-Emmett-Teller(BET),Fourier transform infrared spectroscopy(FTIR),elemental analysis(EA),and X-ray photoelectron spectroscopy(XPS).The characterization test shows that the specific surface area of the sample increases from 1121 to 1523 m^(2)/g,and the ratio of(N+O)/C increases from 10.8%to 30.0%by the glycine modification.After five cycles of adsorption-desorption,the adsorption capacity can still be maintained at 88%of the initial capacity.NOPAC-GLY-60 has excellent adsorption selectivity for Gd(Ⅲ).With the obvious advantages of simple synthesis steps and low cost,the activated carbon modification method adopted in this study has great application value in the field of rare earth adsorption and recovery.展开更多
基金Supported by "863" Project(2008AA10Z153)the National Natural Science Foundation of China(31171578)+1 种基金Heilongjiang Provincial Higher School Science and Technology Innovation Team Building Program(2011TD005)the National Basic Scientific Talent Training Fund Projects(J1210069)
文摘The enzyme myo-inositol-1-phosphate synthase(MIPS EC 5.5.1.4) catalyzes the first step of myo-inositol biosynthesis, a product that plays crucial roles in plants as an osmoprotectant, transduction molecule, cell wall constituent and production of stress related molecule. Previous reports highlighted an important role of MIPS family genes in abiotic stresses particularly under salt stress tolerance in several plant species; however, little is known about the cellular and physiological functions of MIPS2 genes under abiotic conditions. In this study, a novel salt stress responsive gene designated Gs MIPS2 from wild soybean Glycine soja 07256 was functionally characterized contained an open reading frame(ORF) of 1 533 bp coding a peptide sequence of 510 amino acids along with mass of 56 445 ku. Multiple sequence alignment analysis revealed its 92%-99% similarity with other MIPS family members in legume proteins. Quantitative real-time PCR results demonstrated that Gs MIPS2 was induced by salt stress and expressed in roots of soybean. The positive function of Gs MIPS2 under salt response at different growth stages of transgenic Arabidopsis was also elucidated. The results showed that Gs MIPS2 transgenic lines displayed increased tolerance as compared to WT and atmips2 mutant lines under salt stress. Furthermore, the expression levels of some salt stress responsive marker genes, including KIN1, RD29 A, RD29 B, P5 Cs and COR47 were significantly up-regulated in Gs MIPS2 overexpression lines than wild type and atmips2 mutant. Collectively, these results suggested that Gs MIPS2 gene was a positive regulator of plant tolerance to salt stress. This was the first report to demonstrate that overexpression of Gs MIPS2 gene from wild soybean improved salt tolerance in transgenic Arabidopsis.
基金Project supported by the National Natural Science Foundation of China(41662004)。
文摘Glycine functionalized activated carbon adsorption material(NOPAC-GLY-X)was successfully prepared by one-step thermal decomposition using agricultural waste navel orange peel as a precursor.Through batch adsorption experiments,it is found that the adsorption performance of Gd(Ⅲ)on activated carbon can be significantly enhanced by glycine modification.The adsorption isotherms of the NOPACs conform to the Langmuir isotherm model,and the maximum adsorption capacity of the activated carbon sample NOPAC-Gly-60 is approximately 48.5 mg/g.The Gd(Ⅲ)adsorption capacity of navel orange peel activated carbon can be doubled after glycine modification,and the adsorption efficiency of gadolinium can reach99%at pH=7.The physicochemical properties of the prepared adsorbents were characterized by Brunauer-Emmett-Teller(BET),Fourier transform infrared spectroscopy(FTIR),elemental analysis(EA),and X-ray photoelectron spectroscopy(XPS).The characterization test shows that the specific surface area of the sample increases from 1121 to 1523 m^(2)/g,and the ratio of(N+O)/C increases from 10.8%to 30.0%by the glycine modification.After five cycles of adsorption-desorption,the adsorption capacity can still be maintained at 88%of the initial capacity.NOPAC-GLY-60 has excellent adsorption selectivity for Gd(Ⅲ).With the obvious advantages of simple synthesis steps and low cost,the activated carbon modification method adopted in this study has great application value in the field of rare earth adsorption and recovery.