Alkali stress is a major constraint for crop production in many regions of saline-alkali land.However,little is known about the mechanisms through which wheat responds to alkali stress.In this study,we identified a ca...Alkali stress is a major constraint for crop production in many regions of saline-alkali land.However,little is known about the mechanisms through which wheat responds to alkali stress.In this study,we identified a calcium ion-binding protein from wheat,TaCCD1,which is critical for regulating the plasma membrane(PM)H^(+)-ATPase-mediated alkali stress response.PM H+-ATPase activity is closely related to alkali tolerance in the wheat variety Shanrong 4(SR4).We found that two D-clade type 2C protein phosphatases,TaPP2C.D1 and TaPP2C.D8(TaPP2C.D1/8),negatively modulate alkali stress tolerance by dephosphorylating the penultimate threonine residue(Thr926)of TaHA2 and thereby inhibiting PM H+-ATPase activity.Alkali stress induces the expression of TaCCD1 in SR4,and TaCCD1 interacts with TaSAUR215,an early auxin-responsive protein.These responses are both dependent on calcium signaling triggered by alkali stress.TaCCD1 enhances the inhibitory effect of TaSAUR215 on TaPP2C.D1/8 activity,thereby promoting the activity of the PM H^(+)-ATPase TaHA2 and alkali stress tolerance in wheat.Functional and genetic analyses verified the effects of these genes in response to alkali stress,indicating that TaPP2C.D1/8 function downstream of TaSAUR215 and TaCCD1.Collectively,this study uncovers a new signaling pathway that regulates wheat responses to alkali stress,in which Ca^(2+)-dependent TaCCD1 cooperates with TaSAUR215 to enhance PM H+-ATPase activity and alkali stress tolerance by inhibiting TaPP2C.D1/8-mediated dephosphorylation of PM H+-ATPase TaHA2 in wheat.展开更多
A bifunctional catalyst Pt/HY-β was prepared from a bimicroporous composite zeolite Y-β. Characterization results showed that the specific surface area, pore volume, and acid amount of the catalyst Pt/HY-β all decr...A bifunctional catalyst Pt/HY-β was prepared from a bimicroporous composite zeolite Y-β. Characterization results showed that the specific surface area, pore volume, and acid amount of the catalyst Pt/HY-β all decreased compared to the original zeolite. The catalytic performance of this catalyst in n-octane hydroisomerization was investigated in a fixed bed stainless steel tubular reactor. The results showed that at a hydrogen/n-octane volume ratio of 1000, pressure of 0.6 MPa, temperature of 230 ℃ and LHSV of 3 h^-1, the conversion of n-octane, yield of liquid, hydrocracking rate and yield of iso-octane were 52.32%, 88.66%, 12.60%, 39.51%, respectively.展开更多
The effect of Pd addition on the glass-forming ability and thermal stability of the Zr55Al10Cu30Ni5-xPdx (x=0, 1, 3, 5 at. pct) alloys upon copper-mold casting has been investigated. The structure, thermal stability a...The effect of Pd addition on the glass-forming ability and thermal stability of the Zr55Al10Cu30Ni5-xPdx (x=0, 1, 3, 5 at. pct) alloys upon copper-mold casting has been investigated. The structure, thermal stability and microstructure were studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and transmission electron microscopy (TEM), respectively. It was identified that a new bulk amorphous alloy with the larger supercooled liquid region Tx of 100 K is obtained with substituting Ni by 1 at. pct Pd. Furthermore, the origins that thermal stability and GFA change with increasing of Pd have also beer discussed.展开更多
The degradation of acid orange II(AO II)by a nanoporous Fe-Si-B(NP-Fe Si B)electrode under the pulsed square-wave potential has been investigated in this research.Defect-enriched NP-Fe Si B electrode was fabricated th...The degradation of acid orange II(AO II)by a nanoporous Fe-Si-B(NP-Fe Si B)electrode under the pulsed square-wave potential has been investigated in this research.Defect-enriched NP-Fe Si B electrode was fabricated through dealloying of annealed Fe_(76)Si_(9)B_(15)amorphous ribbons.The results of UV-vis spectra and FTIR indicated that AO II solution was degraded efficiently into unharmful molecules H_(2)O and CO_(2)on NPFe Si B electrode within 5 mins under the square-wave potential of±1.5 V.The degradation efficiency of the NP-Fe Si B electrode remains 98.9%even after 5-time recycling.The large amount of active surface area of the nanoporous Fe Si B electrode with lattice disorders and stacking faults,and alternate electrochemical redox reactions were mainly responsible for the excellent degradation performance of the NP-Fe Si B electrode.The electrochemical pulsed square-wave process accelerated the redox of Fe element in Fe-based nanoporous electrode and promoted the generation of hydroxyl radicals(·OH)with strong oxidizability as predominant oxidants for the degradation of azo dye molecules,which was not only beneficial to improving the catalytic degradation activity,but also beneficial to enhancing the reusability of the nanoporous electrode.This work provides a highly possibility to efficiently degrade azo dyes and broadens the application fields of nanoporous metals.展开更多
基金supported by grants from the Natural Science Foundation of Shandong Province(ZR2020JQ14 and ZR2019ZD16)the National Natural Science Foundation of China(31872864,32171935,31722038,31720103910,and U1906202)+2 种基金the Agricultural Variety Improvement Project of Shandong Province(2022LZGC002)the National Key Research and Development Program of China(2022YFD1201700)the Project for Scientific Research Innovation Team of Young Scholar in Colleges and Universities of Shandong Province(2020KJE002).
文摘Alkali stress is a major constraint for crop production in many regions of saline-alkali land.However,little is known about the mechanisms through which wheat responds to alkali stress.In this study,we identified a calcium ion-binding protein from wheat,TaCCD1,which is critical for regulating the plasma membrane(PM)H^(+)-ATPase-mediated alkali stress response.PM H+-ATPase activity is closely related to alkali tolerance in the wheat variety Shanrong 4(SR4).We found that two D-clade type 2C protein phosphatases,TaPP2C.D1 and TaPP2C.D8(TaPP2C.D1/8),negatively modulate alkali stress tolerance by dephosphorylating the penultimate threonine residue(Thr926)of TaHA2 and thereby inhibiting PM H+-ATPase activity.Alkali stress induces the expression of TaCCD1 in SR4,and TaCCD1 interacts with TaSAUR215,an early auxin-responsive protein.These responses are both dependent on calcium signaling triggered by alkali stress.TaCCD1 enhances the inhibitory effect of TaSAUR215 on TaPP2C.D1/8 activity,thereby promoting the activity of the PM H^(+)-ATPase TaHA2 and alkali stress tolerance in wheat.Functional and genetic analyses verified the effects of these genes in response to alkali stress,indicating that TaPP2C.D1/8 function downstream of TaSAUR215 and TaCCD1.Collectively,this study uncovers a new signaling pathway that regulates wheat responses to alkali stress,in which Ca^(2+)-dependent TaCCD1 cooperates with TaSAUR215 to enhance PM H+-ATPase activity and alkali stress tolerance by inhibiting TaPP2C.D1/8-mediated dephosphorylation of PM H+-ATPase TaHA2 in wheat.
基金sponsored by China Petroleumand Chemical Corporation(No.:090701)
文摘A bifunctional catalyst Pt/HY-β was prepared from a bimicroporous composite zeolite Y-β. Characterization results showed that the specific surface area, pore volume, and acid amount of the catalyst Pt/HY-β all decreased compared to the original zeolite. The catalytic performance of this catalyst in n-octane hydroisomerization was investigated in a fixed bed stainless steel tubular reactor. The results showed that at a hydrogen/n-octane volume ratio of 1000, pressure of 0.6 MPa, temperature of 230 ℃ and LHSV of 3 h^-1, the conversion of n-octane, yield of liquid, hydrocracking rate and yield of iso-octane were 52.32%, 88.66%, 12.60%, 39.51%, respectively.
基金The authors are grateful to the financial support by the National Key Basic Research and Development Program of China(No.G200067201)National High Technical Research Development Program of China(No.2001AA331010)for this research.
文摘The effect of Pd addition on the glass-forming ability and thermal stability of the Zr55Al10Cu30Ni5-xPdx (x=0, 1, 3, 5 at. pct) alloys upon copper-mold casting has been investigated. The structure, thermal stability and microstructure were studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and transmission electron microscopy (TEM), respectively. It was identified that a new bulk amorphous alloy with the larger supercooled liquid region Tx of 100 K is obtained with substituting Ni by 1 at. pct Pd. Furthermore, the origins that thermal stability and GFA change with increasing of Pd have also beer discussed.
基金financially supported by Shi-changxu Innovation Center for Advanced Materials,Institute of Metal Research,Chinese Academy of Sciences,the National Natural Science Foundation of China(51790484,51671106)Chinese Academy of Sciences(ZDBSLY-JSC023)Fundamental Research Funds for the Central Universities(30919011404)。
文摘The degradation of acid orange II(AO II)by a nanoporous Fe-Si-B(NP-Fe Si B)electrode under the pulsed square-wave potential has been investigated in this research.Defect-enriched NP-Fe Si B electrode was fabricated through dealloying of annealed Fe_(76)Si_(9)B_(15)amorphous ribbons.The results of UV-vis spectra and FTIR indicated that AO II solution was degraded efficiently into unharmful molecules H_(2)O and CO_(2)on NPFe Si B electrode within 5 mins under the square-wave potential of±1.5 V.The degradation efficiency of the NP-Fe Si B electrode remains 98.9%even after 5-time recycling.The large amount of active surface area of the nanoporous Fe Si B electrode with lattice disorders and stacking faults,and alternate electrochemical redox reactions were mainly responsible for the excellent degradation performance of the NP-Fe Si B electrode.The electrochemical pulsed square-wave process accelerated the redox of Fe element in Fe-based nanoporous electrode and promoted the generation of hydroxyl radicals(·OH)with strong oxidizability as predominant oxidants for the degradation of azo dye molecules,which was not only beneficial to improving the catalytic degradation activity,but also beneficial to enhancing the reusability of the nanoporous electrode.This work provides a highly possibility to efficiently degrade azo dyes and broadens the application fields of nanoporous metals.