Compound-specific stable isotope analysis of individual amino acids(CSIA-AA)has been widely used in ecological and biogeochemical studies.It has been proven to be powerful in tracing the diet sources and trophic inter...Compound-specific stable isotope analysis of individual amino acids(CSIA-AA)has been widely used in ecological and biogeochemical studies.It has been proven to be powerful in tracing the diet sources and trophic interactions.However,assessing the N sources of mesopelagic fishes has been inconclusive because the mesopelagic fishes’unique domain(water depth ranged from 0 to 1000 m)and unresolved nitrogen isotopes of various forms.This study proposes a new method for coupling instruments(ion chromatography and PreconIRMS)and chemical method of oxidation-reduction of amino acids,and also combinedδ15N of AAs withδ13C of fatty acids(FAs)to analyze the trophic interactions of mesopelagic fishes in the South China Sea(SCS).AAs were isolated by ion chromatography with high peak resolution and collected by an automated fraction collector.The chemical method then converted the AAs into N2 O with a robust oxidation yields and suitable molar ratio of NH2 OH to.Finally,theδ15N of AAs at 20 nmol were measured with a reasonable precision(<0.6‰).With this method,this study report the first batch high precisionδ15N of AAs andδ13C of FAs of mesopelagic fishes collected from SCS.Diaphus luetkeni,Chauliodus minimus and Bathygadus antrodes showed similarδ13C values of 20:4 n-6(~-28‰),while Argyropelecus affinis and Stomias had similar values(~-32‰).These results reflect that mesopelagic fishes had complex diet sources.An increase of 4‰inδ15N of glutamic acid(Glu)was found between piscivorous and planktivorous fishes,which might suggest a trophic discrimination factor of mesopelagic fishes in the SCS.This study usedδ13C of 20:4 n-6 to reveal the diet sources of mesopelagic fishes andδ15N of Glu to clarify trophic level between piscivorous and planktivorous fishes.Thus,this combinative method could therefore ultimately be applied in a variety of deep-sea ecosystem.展开更多
【目的】利用气相色谱-燃烧-同位素比值质谱仪(gas chromatography-combustion-isotope ratio masss pectrometry,GC-C-IRMS)测定小麦籽粒氨基酸碳氮稳定同位素组成。【方法】以小麦临汾50744为材料,水解得到其籽粒蛋白质氨基酸,将氨基...【目的】利用气相色谱-燃烧-同位素比值质谱仪(gas chromatography-combustion-isotope ratio masss pectrometry,GC-C-IRMS)测定小麦籽粒氨基酸碳氮稳定同位素组成。【方法】以小麦临汾50744为材料,水解得到其籽粒蛋白质氨基酸,将氨基酸标准样品以及小麦籽粒氨基酸衍生化为N-新戊酰基,O-异丙醇(N-pivaloyl-isopropyl,NPP)氨基酸酯,利用GC-C-IRMS测定其碳氮稳定同位素组成。【结果】氨基酸标准样品的碳氮同位素组成分析表明,NPP氨基酸酯的平均重现性δ13C为0.47‰,δ15N为0.28‰,并没有产生大的同位素分馏,因此δ13C和δ15N都能得到满意的测定结果。运用GC-C-IRMS测定了小麦临汾50744籽粒蛋白质氨基酸的稳定碳氮同位素的自然丰度,其中δ13C的变化范围在-28.7‰到-34.7‰,δ15N的变化范围为-6.2‰到9.5‰。采用系统聚类分析进行分类,根据δ13C可以将氨基酸分为两类;根据δ15N可以将氨基酸分为三类。【结论】运用GC-C-IRMS结合NPP氨基酸酯衍生物可以测定小麦籽粒氨基酸的稳定碳氮同位素,这对于揭示氨基酸代谢途径的差异以及逆境胁迫下氨基酸的合成差异具有重要的意义。展开更多
7-epi-Taxane has been achieved efficiently in gram scale from natural taxane via inversion of the 7-hydroxyl group simply using Ag20 as catalyst and DMF as solvent. The catalyst could he quantitatively recovered by fi...7-epi-Taxane has been achieved efficiently in gram scale from natural taxane via inversion of the 7-hydroxyl group simply using Ag20 as catalyst and DMF as solvent. The catalyst could he quantitatively recovered by filtra- tion without loss of catalytic activity. This condition is also applicable to the direct epimerization of taxane derivatives （e.g., docetaxel and paclitaxel） to 7-epi-taxane derivatives （e.g., 7-epi-docetaxel and 7-epi-paclitaxel）. Furthermore, 33 ester derivatives of 7-epi-taxane with different amino acid moieties at the position of C-13 were successfully synthesized via esterification without protecting C-7-OH. Bioassay results revealed that compounds 13 and 18 have good selectivity against prostatic cancer cell line DU145, with ICs0 value as low as 15.9 nmol/L for 18.展开更多
基金The National Basic Research Program(973 Program)of China under contract No.2014CB441502the National Natural Science Foundation of China under contract No.41876074the Cross-research Center Project by QNLM under contract No.JCZX202007。
文摘Compound-specific stable isotope analysis of individual amino acids(CSIA-AA)has been widely used in ecological and biogeochemical studies.It has been proven to be powerful in tracing the diet sources and trophic interactions.However,assessing the N sources of mesopelagic fishes has been inconclusive because the mesopelagic fishes’unique domain(water depth ranged from 0 to 1000 m)and unresolved nitrogen isotopes of various forms.This study proposes a new method for coupling instruments(ion chromatography and PreconIRMS)and chemical method of oxidation-reduction of amino acids,and also combinedδ15N of AAs withδ13C of fatty acids(FAs)to analyze the trophic interactions of mesopelagic fishes in the South China Sea(SCS).AAs were isolated by ion chromatography with high peak resolution and collected by an automated fraction collector.The chemical method then converted the AAs into N2 O with a robust oxidation yields and suitable molar ratio of NH2 OH to.Finally,theδ15N of AAs at 20 nmol were measured with a reasonable precision(<0.6‰).With this method,this study report the first batch high precisionδ15N of AAs andδ13C of FAs of mesopelagic fishes collected from SCS.Diaphus luetkeni,Chauliodus minimus and Bathygadus antrodes showed similarδ13C values of 20:4 n-6(~-28‰),while Argyropelecus affinis and Stomias had similar values(~-32‰).These results reflect that mesopelagic fishes had complex diet sources.An increase of 4‰inδ15N of glutamic acid(Glu)was found between piscivorous and planktivorous fishes,which might suggest a trophic discrimination factor of mesopelagic fishes in the SCS.This study usedδ13C of 20:4 n-6 to reveal the diet sources of mesopelagic fishes andδ15N of Glu to clarify trophic level between piscivorous and planktivorous fishes.Thus,this combinative method could therefore ultimately be applied in a variety of deep-sea ecosystem.
文摘【目的】利用气相色谱-燃烧-同位素比值质谱仪(gas chromatography-combustion-isotope ratio masss pectrometry,GC-C-IRMS)测定小麦籽粒氨基酸碳氮稳定同位素组成。【方法】以小麦临汾50744为材料,水解得到其籽粒蛋白质氨基酸,将氨基酸标准样品以及小麦籽粒氨基酸衍生化为N-新戊酰基,O-异丙醇(N-pivaloyl-isopropyl,NPP)氨基酸酯,利用GC-C-IRMS测定其碳氮稳定同位素组成。【结果】氨基酸标准样品的碳氮同位素组成分析表明,NPP氨基酸酯的平均重现性δ13C为0.47‰,δ15N为0.28‰,并没有产生大的同位素分馏,因此δ13C和δ15N都能得到满意的测定结果。运用GC-C-IRMS测定了小麦临汾50744籽粒蛋白质氨基酸的稳定碳氮同位素的自然丰度,其中δ13C的变化范围在-28.7‰到-34.7‰,δ15N的变化范围为-6.2‰到9.5‰。采用系统聚类分析进行分类,根据δ13C可以将氨基酸分为两类;根据δ15N可以将氨基酸分为三类。【结论】运用GC-C-IRMS结合NPP氨基酸酯衍生物可以测定小麦籽粒氨基酸的稳定碳氮同位素,这对于揭示氨基酸代谢途径的差异以及逆境胁迫下氨基酸的合成差异具有重要的意义。
文摘7-epi-Taxane has been achieved efficiently in gram scale from natural taxane via inversion of the 7-hydroxyl group simply using Ag20 as catalyst and DMF as solvent. The catalyst could he quantitatively recovered by filtra- tion without loss of catalytic activity. This condition is also applicable to the direct epimerization of taxane derivatives （e.g., docetaxel and paclitaxel） to 7-epi-taxane derivatives （e.g., 7-epi-docetaxel and 7-epi-paclitaxel）. Furthermore, 33 ester derivatives of 7-epi-taxane with different amino acid moieties at the position of C-13 were successfully synthesized via esterification without protecting C-7-OH. Bioassay results revealed that compounds 13 and 18 have good selectivity against prostatic cancer cell line DU145, with ICs0 value as low as 15.9 nmol/L for 18.
