[Objective] The study aimed to investigate the changes of water status and different responses of osmoregulants during air-drought stress,to better understand mechanisms of drought resistance in Jatropha Curcas L. [Me...[Objective] The study aimed to investigate the changes of water status and different responses of osmoregulants during air-drought stress,to better understand mechanisms of drought resistance in Jatropha Curcas L. [Methods] The 12-day-old J. curcas seedlings were held in a climate chamber at 25/20 ℃(day/night),16 hours illumination,and 75% of relative humidity for air-drought treatment,and the changes of water potential,osmotic potential and the content of soluble sugar,proline,betaine were measured. [Results] Water potential and osmotic potential in leaves of J. curcas seedlings dropped significantly,pressure potential lost during air-drought stress,and the contents of osmoregulants soluble sugar,proline and betaine rose significantly to different extent in the leaves and stems. [Conclusion] Osmoregulants in the leaves and stems respond differently to air-drought stress,and in general leaves are much more responsive to the drought than stems of J. curcas seedlings.展开更多
Yunnan Province is the main distributing area ofJatropha curcas L. This plant is abundant in several drainage areas of the dry-hot, dry-warm and sub-humid valleys in the south subtropical area of Yunnan Province. The ...Yunnan Province is the main distributing area ofJatropha curcas L. This plant is abundant in several drainage areas of the dry-hot, dry-warm and sub-humid valleys in the south subtropical area of Yunnan Province. The seeds that were picked from trees blossoming between April and May and fructifying between September and October will have large seed yield and fine quality. For developing bio-diesel stock forest ofJ. curcas in areas with adaptive climate, seeding measures for afforestation should be taken and techniques on breeding, fast-growing, and high-yielding plantation cultivation are very important.展开更多
Biodiesel produced from crude Jatropha curcas L.oil with trace sulfuric acid catalyst(0.02%-0.08% oil) was investigated at 135-184 ℃.Both esterification and transesterification can be well carried out simultane-ously...Biodiesel produced from crude Jatropha curcas L.oil with trace sulfuric acid catalyst(0.02%-0.08% oil) was investigated at 135-184 ℃.Both esterification and transesterification can be well carried out simultane-ously.Factors affecting the process were investigated,which included the reaction temperature,reaction time,the molar ratio of alcohol to oil,catalyst amount,water content,free fatty acid(FFA) and fatty acid methyl ester(FAME) content.Under the conditions at 165 ℃,0.06%(by mass) H2SO4 of the oil mass,1.6 MPa and 20:1 methanol/oil ratio,the yield of glycerol reached 84.8% in 2 hours.FFA and FAME showed positive effect on the transesterification in certain extent.The water mass content below 1.0% did not show a noticeable effect on trans-esterification.Reaction kinetics in the range of 155 ℃ to 175 ℃ was also measured.展开更多
Jatropha curcas L. (JCL) seeds were extracted and transesterified in-situ using supercritical methanol extraction in the absence of catalyst at different temperatures (200-280℃) and pressures (8-12 MPa), and at...Jatropha curcas L. (JCL) seeds were extracted and transesterified in-situ using supercritical methanol extraction in the absence of catalyst at different temperatures (200-280℃) and pressures (8-12 MPa), and at a fixed reaction time of 30 min with seeds-to-methanol ratio of 1:40 w/v. Design of experiment approach using five-level-two-factors design of Response Surface Methodology (RSM) was used to observe the effect of two independent variables i.e. temperature and pressure and the percent of biodiesel yield which required 13 runs. For optimization of the variables, Central Composite Rotatable Design (CCRD) was used for regression analysis and analysis of variance (ANOVA). The optimize conditions suggested by RSM were at T = 280℃ and P = 12.04 MPa. The predicted and experimental biodicsel yields were found to be 56.8% and 59.9%, respectively, with relatively small deviation errors of 1.59%.展开更多
Jatropha curcas was taken as the test material,6 concentrations including 0,25,50,100,200 and 400μmol/L AlCl3,plus 3 time gradients including 7,14 and 21 d,were set to study the effects of Al^(3+)stress on the antiox...Jatropha curcas was taken as the test material,6 concentrations including 0,25,50,100,200 and 400μmol/L AlCl3,plus 3 time gradients including 7,14 and 21 d,were set to study the effects of Al^(3+)stress on the antioxidant system of Jatropha curcas L.seedling.The results showed that with the Al^(3+)treatment being applied,protein content increased first,then decreased and finally increased with the increase of Al^(3+)concentration;the soluble sugar content increased first and then decreased with the increase of Al^(3+)concentration.Under low concentration of Al^(3+)treatment,Pro content,MDA content and POD activity of Jatropha curcas L.seedling leaves changed a little,while under high concentration of Al^(3+)treatment,Pro and MDA content of Jatropha curcas L.seedling leaves rapidly accumulated,POD activity increased and they showed a trend of increase with the increase of Al^(3+)concentration;From the perspective of Al^(3+)stress time,protein content,soluble sugar content,MDA content and POD activity increased with stress time being prolonged,while Pro content decreased with stress time being prolonged.These results indicated that the leaves of Jatropha curcas L.seedlings had certain self-protection and remediation abilities under Al^(3+)stress.展开更多
HXK(Hexokinase)gene family and the role of JcHXK1 in Jatropha curcas L.were explored.Totally 4 HXK genes JcHXK1,JcHXK2,JcHXK3 and JcHKL1 were identified and complete ORF of JcHXK1 was cloned.Functional domain,phylogen...HXK(Hexokinase)gene family and the role of JcHXK1 in Jatropha curcas L.were explored.Totally 4 HXK genes JcHXK1,JcHXK2,JcHXK3 and JcHKL1 were identified and complete ORF of JcHXK1 was cloned.Functional domain,phylogenetic evolution and low-temperature expression characteristics were analyzed.Results showed that full-length JcHXK1 cDNA was 1497 bp,encoding 498 amino acids with molecular weight of 53.81 kDa and pI of 5.03.Further phylogenetic evolutionary analysis demonstrated HXK1 protein was clustered into 6 small branches and 2 large branches.Sequence alignment showed that HXK1 contained several conserved glycine residues and hydrophobic channels.Prokaryotic expression vector of JcHXK1 was constructed and 12%SDS-PAGE detection showed that it was highly expressed in E.coli.These research was expected to lay a foundation for further gene functional verification and cold signal transduction mechanism for HXK1 in Jatropha curcas L.展开更多
Objective:To investigate the chemical constituents from the leaves of Jatropha curcas and evaluate their inhibition on lipopolysaccharide(LPS)-activated BV-2 microglia cells.Methods:The n-BuOH extract of the leaves of...Objective:To investigate the chemical constituents from the leaves of Jatropha curcas and evaluate their inhibition on lipopolysaccharide(LPS)-activated BV-2 microglia cells.Methods:The n-BuOH extract of the leaves of J.curcas was isolated by macroporous adsorption resin,silica gel,ODS,column chromatography and semi-preparative HPLC.The structures of the compounds were identified by MS,NMR,ECD,and other spectroscopic methods.In addition,anti-neuroinflammatory effects of isolated compounds were evaluated by measuring the production of nitric oxide(NO)in overactivated BV-2 cells.Results:Seventeen compounds,including(7R,8S)-crataegifin A-4-O-β-D-glucopyranoside(1),(8R,8’R)-arctigenin(2),arctigenin-4’-O-β-D-glucopyranoside(3),(-)-syringaresinol(4),syringaresinol-4’-O-β-Dglucopyranoside(5),(-)-pinoresinol(6),pinoresinol-4’-O-β-D-glucopyranoside(7),buddlenol D(8),(2R,3R)-dihydroquercetin(9),(2S,3S)-epicatechin(10),(2R,3S)-catechin(11),isovitexin(12),naringenin-7-O-β-D-glucopyranoside(13),chamaejasmin(14),neochamaejasmin B(15),isoneochamaejasmin A(16),and tomentin-5-O-β-D-glucopyranoside(17)were isolated and identified.Compounds 2,4and 8 significantly inhibited the release of NO in BV-2 microglia activated by LPS,with IC50values of18.34,29.33 and 26.30μmol/L,respectively.Conclusion:Compound 1 is a novel compound,and compounds 2,3,8,14–17 are isolated from Jatropha genus for the first time.In addition,the lignans significantly inhibited NO release and the inhibitory activity was decreased after glycosylation.展开更多
基金Supported by Special Key R&D Fund from Yunnan Provincial Department of Education (ZD2010004)~~
文摘[Objective] The study aimed to investigate the changes of water status and different responses of osmoregulants during air-drought stress,to better understand mechanisms of drought resistance in Jatropha Curcas L. [Methods] The 12-day-old J. curcas seedlings were held in a climate chamber at 25/20 ℃(day/night),16 hours illumination,and 75% of relative humidity for air-drought treatment,and the changes of water potential,osmotic potential and the content of soluble sugar,proline,betaine were measured. [Results] Water potential and osmotic potential in leaves of J. curcas seedlings dropped significantly,pressure potential lost during air-drought stress,and the contents of osmoregulants soluble sugar,proline and betaine rose significantly to different extent in the leaves and stems. [Conclusion] Osmoregulants in the leaves and stems respond differently to air-drought stress,and in general leaves are much more responsive to the drought than stems of J. curcas seedlings.
文摘Yunnan Province is the main distributing area ofJatropha curcas L. This plant is abundant in several drainage areas of the dry-hot, dry-warm and sub-humid valleys in the south subtropical area of Yunnan Province. The seeds that were picked from trees blossoming between April and May and fructifying between September and October will have large seed yield and fine quality. For developing bio-diesel stock forest ofJ. curcas in areas with adaptive climate, seeding measures for afforestation should be taken and techniques on breeding, fast-growing, and high-yielding plantation cultivation are very important.
基金Supported by the Key Grant Project of Chinese Ministry of Education (307023)the National Natural Science Foundation of China (20976108)the National Key Technology Research and Development Program (2007BAD50D05)
文摘Biodiesel produced from crude Jatropha curcas L.oil with trace sulfuric acid catalyst(0.02%-0.08% oil) was investigated at 135-184 ℃.Both esterification and transesterification can be well carried out simultane-ously.Factors affecting the process were investigated,which included the reaction temperature,reaction time,the molar ratio of alcohol to oil,catalyst amount,water content,free fatty acid(FFA) and fatty acid methyl ester(FAME) content.Under the conditions at 165 ℃,0.06%(by mass) H2SO4 of the oil mass,1.6 MPa and 20:1 methanol/oil ratio,the yield of glycerol reached 84.8% in 2 hours.FFA and FAME showed positive effect on the transesterification in certain extent.The water mass content below 1.0% did not show a noticeable effect on trans-esterification.Reaction kinetics in the range of 155 ℃ to 175 ℃ was also measured.
文摘Jatropha curcas L. (JCL) seeds were extracted and transesterified in-situ using supercritical methanol extraction in the absence of catalyst at different temperatures (200-280℃) and pressures (8-12 MPa), and at a fixed reaction time of 30 min with seeds-to-methanol ratio of 1:40 w/v. Design of experiment approach using five-level-two-factors design of Response Surface Methodology (RSM) was used to observe the effect of two independent variables i.e. temperature and pressure and the percent of biodiesel yield which required 13 runs. For optimization of the variables, Central Composite Rotatable Design (CCRD) was used for regression analysis and analysis of variance (ANOVA). The optimize conditions suggested by RSM were at T = 280℃ and P = 12.04 MPa. The predicted and experimental biodicsel yields were found to be 56.8% and 59.9%, respectively, with relatively small deviation errors of 1.59%.
文摘Jatropha curcas was taken as the test material,6 concentrations including 0,25,50,100,200 and 400μmol/L AlCl3,plus 3 time gradients including 7,14 and 21 d,were set to study the effects of Al^(3+)stress on the antioxidant system of Jatropha curcas L.seedling.The results showed that with the Al^(3+)treatment being applied,protein content increased first,then decreased and finally increased with the increase of Al^(3+)concentration;the soluble sugar content increased first and then decreased with the increase of Al^(3+)concentration.Under low concentration of Al^(3+)treatment,Pro content,MDA content and POD activity of Jatropha curcas L.seedling leaves changed a little,while under high concentration of Al^(3+)treatment,Pro and MDA content of Jatropha curcas L.seedling leaves rapidly accumulated,POD activity increased and they showed a trend of increase with the increase of Al^(3+)concentration;From the perspective of Al^(3+)stress time,protein content,soluble sugar content,MDA content and POD activity increased with stress time being prolonged,while Pro content decreased with stress time being prolonged.These results indicated that the leaves of Jatropha curcas L.seedlings had certain self-protection and remediation abilities under Al^(3+)stress.
基金supported by the National Natural Science Foundation of China(31460179,2017FG001-51)。
文摘HXK(Hexokinase)gene family and the role of JcHXK1 in Jatropha curcas L.were explored.Totally 4 HXK genes JcHXK1,JcHXK2,JcHXK3 and JcHKL1 were identified and complete ORF of JcHXK1 was cloned.Functional domain,phylogenetic evolution and low-temperature expression characteristics were analyzed.Results showed that full-length JcHXK1 cDNA was 1497 bp,encoding 498 amino acids with molecular weight of 53.81 kDa and pI of 5.03.Further phylogenetic evolutionary analysis demonstrated HXK1 protein was clustered into 6 small branches and 2 large branches.Sequence alignment showed that HXK1 contained several conserved glycine residues and hydrophobic channels.Prokaryotic expression vector of JcHXK1 was constructed and 12%SDS-PAGE detection showed that it was highly expressed in E.coli.These research was expected to lay a foundation for further gene functional verification and cold signal transduction mechanism for HXK1 in Jatropha curcas L.
基金financially supported by National Natural Science Foundation of China(No.81872768,U1903122)Shenyang Young Scientific and Technological Innovators Program(No.RC200408)Doctoral Scientific Research Foundation of Liaoning Province(No.2020-BS-129)。
文摘Objective:To investigate the chemical constituents from the leaves of Jatropha curcas and evaluate their inhibition on lipopolysaccharide(LPS)-activated BV-2 microglia cells.Methods:The n-BuOH extract of the leaves of J.curcas was isolated by macroporous adsorption resin,silica gel,ODS,column chromatography and semi-preparative HPLC.The structures of the compounds were identified by MS,NMR,ECD,and other spectroscopic methods.In addition,anti-neuroinflammatory effects of isolated compounds were evaluated by measuring the production of nitric oxide(NO)in overactivated BV-2 cells.Results:Seventeen compounds,including(7R,8S)-crataegifin A-4-O-β-D-glucopyranoside(1),(8R,8’R)-arctigenin(2),arctigenin-4’-O-β-D-glucopyranoside(3),(-)-syringaresinol(4),syringaresinol-4’-O-β-Dglucopyranoside(5),(-)-pinoresinol(6),pinoresinol-4’-O-β-D-glucopyranoside(7),buddlenol D(8),(2R,3R)-dihydroquercetin(9),(2S,3S)-epicatechin(10),(2R,3S)-catechin(11),isovitexin(12),naringenin-7-O-β-D-glucopyranoside(13),chamaejasmin(14),neochamaejasmin B(15),isoneochamaejasmin A(16),and tomentin-5-O-β-D-glucopyranoside(17)were isolated and identified.Compounds 2,4and 8 significantly inhibited the release of NO in BV-2 microglia activated by LPS,with IC50values of18.34,29.33 and 26.30μmol/L,respectively.Conclusion:Compound 1 is a novel compound,and compounds 2,3,8,14–17 are isolated from Jatropha genus for the first time.In addition,the lignans significantly inhibited NO release and the inhibitory activity was decreased after glycosylation.