AIM： To understand the digestive stability and mechanism of release and intestinal uptake of pea ferritin iron in caco-2 cell line model.METHODS： Pea seed ferritin was purified using salt fractionation followed by g...AIM： To understand the digestive stability and mechanism of release and intestinal uptake of pea ferritin iron in caco-2 cell line model.METHODS： Pea seed ferritin was purified using salt fractionation followed by gel filtration chromatography.The bioavailability of ferritin iron was assessed using coupled in vitro digestion/Caco-2 cell model in the presence or absence of ascorbic acid and phytic acid.Caco-2 cell ferritin formation was used as a surrogate marker of iron uptake. Structural changes of pea ferritin under simulated gastric pH were characterized using electrophoresis, gel filtration and circular dichroism spectroscopy.RESULTS： The caco-2 cell ferritin formation was significantly increased （P 〈 0.001） with FeSO4 （19.3±9.8 ng/mg protein） and pea ferritin （13.9 ± 6.19 ng/mg protein） compared to the blank digest （3.7 ± 1.8 ng/mg protein）. Ascorbic acid enhanced while phytic acid decreased the pea ferritin iron bioavailability. However,either in the presence or absence of ascorbic acid, the ferritin content of caco-2 cells was significantly less with pea ferritin than with FeSO4. At gastric pH, no band corresponding to ferritin was observed in the presence of pepsin either on native PAGE or SDS-PAGE. Gel filtration chromatography and circular dichroism spectroscopy revealed a pH dependent loss of quaternary and secondary structure.CONCLUSION： Under gastric conditions, the iron core of pea ferritin is released into the digestive medium due to acid induced structural alterations and dissociation of protein. The released iron interacts with dietary factors leading to modulation of pea ferritin iron bioavailability,resembling the typical characteristics of non-heme iron.展开更多
The bioavailability of 22 heavy metals was investigated at 19 sampling sites in Tieguanyin tea garden in Anxi County,Fujian Province,southeastern China.Heavy metal concentrations were determined by inductively coupled...The bioavailability of 22 heavy metals was investigated at 19 sampling sites in Tieguanyin tea garden in Anxi County,Fujian Province,southeastern China.Heavy metal concentrations were determined by inductively coupled plasma-mass spectrometry(ICP-MS)and evaluated by geo-accumulation index(I_(geo)).Dilute nitric acid extraction was used to evaluate biological activity.Cu,Pb,and Cd were highly bioavailable and most easily absorbed by tea trees.Heavy metal bioavailability in the surface soil was as the ratio of the effective state to the total amount.Cd had the highest I_(geo)values,and the respective samples and sites were classified as moderately/strongly contaminated.Cd element is considered the main factor of heavy metal pollution in the tea garden in Anxi.The other heavy metals studied were present in lower concentrations;thus,the samples were classified as uncontaminated or slightly contaminated.展开更多
The coexistence of magnetic ordering and ferroelectricity, ing on the origin of ferroelectricity, multiferroic materials known as multiferroics, has drawn a lot of research effort. Depend can be classified into differ...The coexistence of magnetic ordering and ferroelectricity, ing on the origin of ferroelectricity, multiferroic materials known as multiferroics, has drawn a lot of research effort. Depend can be classified into different groups. In this paper, we review re cent progress in the field of multiferroics induced by different forms of charge ordering. In addition to a general description of charge order and electronic ferroelectricity, we focus on two specific systems： （1） charge order with frustration in RFe2O4 （R=Lu, Yb） system; （2） charge ordered perovskite manganites of the type （R1-xCax）MnO3 （R=La, Pr）. The charge ordering can be tuned by external electric fields, which results in pronounced magnetoelectric effects and strong dielectric tunability. Other materials and possible candidates with charge order induced multiferroics are also briefly summarized.展开更多
基金Supported by a grant No. BT/PR6728/AGR/02/334/2005 from the Department of Biotechnology, Government of India to KMN and RP, SB is supported by a Research Fellowship from the Indian Council of Medical Research
文摘AIM： To understand the digestive stability and mechanism of release and intestinal uptake of pea ferritin iron in caco-2 cell line model.METHODS： Pea seed ferritin was purified using salt fractionation followed by gel filtration chromatography.The bioavailability of ferritin iron was assessed using coupled in vitro digestion/Caco-2 cell model in the presence or absence of ascorbic acid and phytic acid.Caco-2 cell ferritin formation was used as a surrogate marker of iron uptake. Structural changes of pea ferritin under simulated gastric pH were characterized using electrophoresis, gel filtration and circular dichroism spectroscopy.RESULTS： The caco-2 cell ferritin formation was significantly increased （P 〈 0.001） with FeSO4 （19.3±9.8 ng/mg protein） and pea ferritin （13.9 ± 6.19 ng/mg protein） compared to the blank digest （3.7 ± 1.8 ng/mg protein）. Ascorbic acid enhanced while phytic acid decreased the pea ferritin iron bioavailability. However,either in the presence or absence of ascorbic acid, the ferritin content of caco-2 cells was significantly less with pea ferritin than with FeSO4. At gastric pH, no band corresponding to ferritin was observed in the presence of pepsin either on native PAGE or SDS-PAGE. Gel filtration chromatography and circular dichroism spectroscopy revealed a pH dependent loss of quaternary and secondary structure.CONCLUSION： Under gastric conditions, the iron core of pea ferritin is released into the digestive medium due to acid induced structural alterations and dissociation of protein. The released iron interacts with dietary factors leading to modulation of pea ferritin iron bioavailability,resembling the typical characteristics of non-heme iron.
基金supported by the National Science Foundation of China(21177043,21377042)the National Science Foundation of Fujian Province(2015J01147)+1 种基金Fujian Provincial Key Laboratory of Ecology-Toxicological Effects and Control for Emerging Contaminants(PY16006)the Research Program of Science and Technology of Quanzhou City Government(2012Z86,2014Z130)
文摘The bioavailability of 22 heavy metals was investigated at 19 sampling sites in Tieguanyin tea garden in Anxi County,Fujian Province,southeastern China.Heavy metal concentrations were determined by inductively coupled plasma-mass spectrometry(ICP-MS)and evaluated by geo-accumulation index(I_(geo)).Dilute nitric acid extraction was used to evaluate biological activity.Cu,Pb,and Cd were highly bioavailable and most easily absorbed by tea trees.Heavy metal bioavailability in the surface soil was as the ratio of the effective state to the total amount.Cd had the highest I_(geo)values,and the respective samples and sites were classified as moderately/strongly contaminated.Cd element is considered the main factor of heavy metal pollution in the tea garden in Anxi.The other heavy metals studied were present in lower concentrations;thus,the samples were classified as uncontaminated or slightly contaminated.
基金supported by the National Natural Science Foundation of China (Grant Nos. 11074293,51021061 and 50831006)
文摘The coexistence of magnetic ordering and ferroelectricity, ing on the origin of ferroelectricity, multiferroic materials known as multiferroics, has drawn a lot of research effort. Depend can be classified into different groups. In this paper, we review re cent progress in the field of multiferroics induced by different forms of charge ordering. In addition to a general description of charge order and electronic ferroelectricity, we focus on two specific systems： （1） charge order with frustration in RFe2O4 （R=Lu, Yb） system; （2） charge ordered perovskite manganites of the type （R1-xCax）MnO3 （R=La, Pr）. The charge ordering can be tuned by external electric fields, which results in pronounced magnetoelectric effects and strong dielectric tunability. Other materials and possible candidates with charge order induced multiferroics are also briefly summarized.
