As an important agronomic trait, inclination of leaves is crucial Ior crop architecture and grain yields. 10 understand the molecular mechanism controlling rice leaf angles, one rice leaf inclination2 （1c2, three all...As an important agronomic trait, inclination of leaves is crucial Ior crop architecture and grain yields. 10 understand the molecular mechanism controlling rice leaf angles, one rice leaf inclination2 （1c2, three alleles） mutant was identified and functionally characterized. Compared to wild-type plants, lc2 mutants have enlarged leaf angles due to increased cell division in the adaxial epidermis of lamina joint. The LC2 gene was isolated through positional cloning, and encodes a vernalization insensitive 3-like protein. Complementary expression of LC2 reversed the enlarged leaf angles of lc2 plants, confirming its role in controlling leaf inclination. LC2 is mainly expressed in the lamina joint during leaf development, and particularly, is induced by the phytohormones abscisic acid, gibberellic acid, auxin, and brassinosteroids. LC2 is localized in the nucleus and defects of LC2 result in altered expression of cell division and hormone-responsive genes, indicating an important role of LC2 in regulating leaf inclination and mediating hormone effects.展开更多
The relationship between vernalization requirement and quantitative and qualitative changes in total leaf soluble proteins were determined in one spring （cv. Kohdasht） and two winter （cvs. Sardari and Norstar） cul...The relationship between vernalization requirement and quantitative and qualitative changes in total leaf soluble proteins were determined in one spring （cv. Kohdasht） and two winter （cvs. Sardari and Norstar） cultivars of wheat （Triticum aestivum L.） exposed to 4℃. Plants were sampled on days 2, 14, 21 and 35 of exposure to 4℃. The final leaf number （FLN） was determined throughout the vernalization periods （0, 7, 14, 24, and 35 d） at 4℃. The final leaf number decreased until days 24 and 35 in Sardari and Norstar eultivars, respectively, indicating the vernalization saturation at these times. No clear changes were detected in the final leaf number of Kohdash cultivar, verifying no vernalization requirement for this spring wheat cultivar. Comparing with control, clear cold-induced 2-fold increases in proteins quantity occurred after 48 h following the 4℃-treatment in the leaves of the both winter wheat cultivars but, such response was not detected in the spring cultivar. However, the electrophoretic protein patterns showed between-cultivar and between-temperature treatment differences. With increasing exposure time to 4℃, the winter cultivars tended to produce more HMW polypeptides than the spring cultivar. Similar proteins were induced in both Sardari and Norstar winter wheat cultivars, however, the long vernalization requirement in Norstar resulted in high level and longer duration of expression of cold-induced proteins compared to Sardari with a short vernalization requirement. These observations indicate that vernalization response regulates the expression of low temperature （LT） tolerance proteins and determines the duration of expression of LT- induced proteins.展开更多
Proteomic assessment of low-abundance leaf proteins is hindered by the large quantity of ribulose-1,5-bisphosphate carboxylase/oxygenase （Rubisco） present within plant leaf tissues. In the present study, total prote...Proteomic assessment of low-abundance leaf proteins is hindered by the large quantity of ribulose-1,5-bisphosphate carboxylase/oxygenase （Rubisco） present within plant leaf tissues. In the present study, total proteins were extracted from wheat （Triticum aestivum L.） leaves by a conventional trichloroacetic acid （TCA）/acetone method and a protocol first developed in this work. Phytate/Ca2＋ fractionation and TCA/acetone precipitation were combined to design an improved TCA/acetone method. The extracted proteins were analysed by two-dimensional gel electrophoresis （2-DE）. The resulting 2-DE images were compared to reveal major differences. The results showed that large quantities of Rubisco were deleted from wheat leaf proteins prepared by the improved method. As many as （758±4） protein spots were detected from 2-DE images of protein extracts obtained by the improved method, 130 more than those detected by the TCA/acetone method. Further analysis indicated that more protein spots could be detected at regions of pI 4.00-4.99 and 6.50-7.00 in the improved method-based 2-DE images. Our findings indicated that the improved method is an efficient protein preparation protocol for separating low-abundance proteins in wheat leaf tissues by 2-DE analysis. The proposed protocol is simple, fast, inexpensive and also applicable to protein preparations of other plants.展开更多
[ Objective ] The paper was to explore effects of Echinacea polysaccharide （EPS） on expression of NF-KB protein secreted by LPS-injured IEC-6 cells, and to provide a theoretical basis for clinical application of Ech...[ Objective ] The paper was to explore effects of Echinacea polysaccharide （EPS） on expression of NF-KB protein secreted by LPS-injured IEC-6 cells, and to provide a theoretical basis for clinical application of Echinacea purpurea against bacterial diseases and enhancement of immunity. [ Method] Nucleoprotein extracted from IEC-6 cells in normal control group, LPS group, different concentrations of EPS （50, 100,200,500 μg/mL） ＋ LPS groups were detected by SDS- PAGE electrophoresis, and the content of NF-κB protein was analyzed using western blotting method. [ Result ] The content of NF-KB protein in normal control group was the lowest, while that in LPS group was the highest. The content of NF-κB protein in EPS group gradually decreased with the increasing concentration of EPS. [ Result] The expression of NF-κB protein increased when IEC-6 cells were stimulated by LPS, and EPS could effectively inhibit increased expression of NF- κB protein. With the increasing concentration of EPS, the inhibition effect against increased expression of NF-κB protein gradually strengthened.展开更多
Sweet potato is one of the first natural GMOs, genetically modified 8000 years ago by Agrobacterium rhizogenes as reported recently by Kyndt et al. A section of 10 kbp long DNA (Transferred- DNA or T-DNA) of the Ri (R...Sweet potato is one of the first natural GMOs, genetically modified 8000 years ago by Agrobacterium rhizogenes as reported recently by Kyndt et al. A section of 10 kbp long DNA (Transferred- DNA or T-DNA) of the Ri (Root-inducing) plasmid was transferred to the plant genome by A. rhizo-genes and has been maintained in all 291 hexaploid sweet potato cultivars of the world. The maintenance in the sweet potato genome and expression of two T-DNA genes for tryptophan-2-monooxygenease (iaaM) and for indole-3-acetamide hydrolase (iaaH) are likely to be physiologically significant since these enzymes convert tryptophan to indole-3-acetic acid, a major plant growth hormone auxin. Sweet potato (Ipomoea batatas (L.) Lam) is ranked the third most important root crop after potato and cassava, and the seventh in global food crop production with more than 126 million metric tons. Although sweet potato originated in Central or South America, China currently produces over 86% of world production with 109 million metric tons. In the United States, North Carolina is the leading producer with 38.5% of the 2007 sweet potato production, followed by California, Mississippi, and Louisiana with 23%, 19%, and 15.9%, respectively. Leaf curl virus diseases have been reported in sweet potato throughout the world. One of the causal agents is Sweet potato leaf curl virus (SPLCV) belonging to the genus Begomovirus (family Geminiviridae). Although SPLCV does not cause symptoms on Beauregard, one of the most predominant sweet potato cultivars in the US, it can reduce the yield up to 26%. Serological detection of SPLCV is not currently available due to the difficulties in obtaining purified virions that can be used as antigen for antiserum production. In attempts to obtain the coat protein (CP) of SPLCV for antibody production, primers were designed to amplify the CP gene. This gene was cloned into the expression vector pMAL-c2E as a fusion protein with maltose-binding protein, and transformed into Escherichia coli strain XL1-Blue. After gene induction, a fusion protein of 72 kDa was purified by amylose affinity chromatography. The yield of the purified fusion protein was approximately 200 μg/liter of bacterial culture. Digestion with enterokinase cleaved the fusion protein into a 42.5 kDa maltosebinding protein and a 29.4 kDa protein. The latter protein was identified by mass spectrometry analysis as the coat protein of SPLCV based on the fact that the mass spectrometry elucidated the sequences corresponding to 37% of amino acid positions of the SPLCV coat protein.展开更多
Logistic and exponential approaches have been used to simulate plant growth and leaf area index (LAI) in different growing conditions. The objective of the present study was to develop and evaluate an approach to simu...Logistic and exponential approaches have been used to simulate plant growth and leaf area index (LAI) in different growing conditions. The objective of the present study was to develop and evaluate an approach to simulate maize LAI that expresses key physiological and phonological processes using a minimum entry requirement for Quality Protein maize (QPM) varieties grown in the southwestern region of the DR-Congo. Data for the development and testing of the model were collected manually in experimental plots using a non-destructive method. Simulation results revealed measurable variations between crop seasons (long season A and short season B) and between the two varieties (Mudishi-1 and Mudishi-3) for height, number of visible leaves, and LAI. For both seasons, Mudishi-3, a short stature variety was associated with expected stable yield based on simulation data. In general, the model simulated reliably all the parameters including the LAI. The LAI value for mudishi-1 was higher than that of Mudishi-3. There were significant differences among the model parameters (K, Ti, a, b, Tf) and between the two varieties. In all crop conditions studied and for the two varieties, the senescence rate (a) was higher, while the growth rate (b) was lower compared to the estimates based on the STICS model.展开更多
The leaf is the main organ for rapeseed photosynthesis,and its morphology influences photosynthetic efficiency and supports increased planting density and yield.However,the molecular regulatory mechanism of leaf morph...The leaf is the main organ for rapeseed photosynthesis,and its morphology influences photosynthetic efficiency and supports increased planting density and yield.However,the molecular regulatory mechanism of leaf morphology in Brassica napus is poorly understood,restricting progress in breeding for the trait.We describe a novel dominant mutation,curly leaf 1(cl1),which confers uneven dorsal–ventral axis development,irregular cellular structure and influenced gravitropic response in the seedling stage.The CL1 locus was mapped to a 1.573-Mb interval on chromosome A05 using simple sequence repeat(SSR)markers,and co-segregated with the phenotype of plants in the curly F2 population.A substitution(P62S)was identified in the highly conserved degron motif(GWSPV)of the IAA2 protein in the cl1mutant,and the P62S substitution impaired the interaction between IAA2 and TIR1 in the presence of auxin,influencing auxin signaling.The P62S substitution-induced curly leaf phenotype was verified by ectopic expression of Bna A05.iaa2 in Arabidopsis and B.napus.Our findings explain the function of IAA2 in rapeseed,providing a foundation for future investigation of auxin signaling and the mechanisms underlying leaf development in B.napus.展开更多
According to the preparation method commonly used for soy proteinαbased adhesives,alfalfa leaf protein was used as the raw material to prepare alfalfa leaf protein-based wood adhesive.Differential scanning calorimetr...According to the preparation method commonly used for soy proteinαbased adhesives,alfalfa leaf protein was used as the raw material to prepare alfalfa leaf protein-based wood adhesive.Differential scanning calorimetry analyzer(DSC),X-ray diffraction(XRD)and Fourier transform infrared spectroscopy(FTαIR)were used to characterize properties of the alfalfa leaf protein-based adhesive in this paper.The results revealed the following:(1)Chemical compositions and chemical structures of the alfalfa leaf protein were basically identical with those of the soy protein,both belonging to spherical proteins with the basis and potential for protein adhesives preparation,and spatial cross-linked network structures would be easily formed.(2)Alfalfa leaf protein and soy protein adhesives had the similar curing behaviors,curing temperature of alfalfa leaf protein-based adhesive was relaαtively lower,and the heating rate had minor influence on curing temperature of alfalfa leaf protein-based adhesive.At different heating rates,change tendencies of curing reaction degrees of both the two adhesives were not totally the same.(3)Activation energy and reaction frequency factor of the alfalfa leaf protein-based adhesive were higher than those of soy protein-based adhesive,indicating that the curing reaction of the alfalfa leaf protein adhesive was more difficult than soy protein-based adhesive,thus the dry shear strength and water resistance of alfalfa protein-based adhesive were lower than those of soy protein-based adhesive.Dynamics models of curing reactions of alfalfa leaf protein-based adhesive and soy protein-based adhesive are dα=dt/1.06×10^(13)e^(-97370/RT)(1-α)^(0.938) and dα/dt=1.09×10^(11)e^(-84260/RT) 1-α)^(0.928) respectively.The results of this study will expand the selection of raw materials for protein-based wood adhesives.展开更多
4PU—30[N—phenyl—’N—(2—chloro—4—pyridyl) urea] is a new type of plant growth regulator with cytokinin properties. It has been confirmed to delay rice leaf senescence effectively. In order to elucidate the physi...4PU—30[N—phenyl—’N—(2—chloro—4—pyridyl) urea] is a new type of plant growth regulator with cytokinin properties. It has been confirmed to delay rice leaf senescence effectively. In order to elucidate the physiological role of 4PU—30 in delaying senescence, the changes of protein, nucleic acid contents, and the related activities of degradative enzymes were studied. Shanyou 63, an indica hybrid rice was used for this experiment. In the in vitro experiment, two full—developed leaves from the top during heading stage were collected and cut into 5.0cm segments, They were floated on the surface of distilled water containing 0.1mg/14PU—30 and incubated in darkness at 30 C. The leaves floated on distilled water were used as control.It was observed that chlorophyll content in controlled leaves declined rapidly started from the second day and dropped by 93.4% on the 6th day while that in leaves treated with 4PU—30 declined by 41.4% only. During senescence, specific activities of hemoglobin—digesting展开更多
Guava leaf tea has been used as a folk medicine for treating hyperglycemic conditions in Asia and Africa. The hypoglycemic efficacy of guava leaf has been documented by many scientists in these regions, but the hypogl...Guava leaf tea has been used as a folk medicine for treating hyperglycemic conditions in Asia and Africa. The hypoglycemic efficacy of guava leaf has been documented by many scientists in these regions, but the hypoglycemic mechanism is poorly understood. Guava leaves were extracted with methanol and the crude extract was partitioned against hexane, ethyl acetate, and butanol in sequence. The leftover in water is defined as the aqueous partition. A second smaller batch was extracted with hot water directly. Oral glucose tolerance test was carried out on healthy mice instead of diabetic mice that lack endogenous insulin. Glucose uptake was examined with 3T3-L1 adipocytes. Oxidative effect on PTP1B （protein tyrosine phosphatase 1b） was carried out with real-time PTP1B enzymatic assay. The aqueous partition of guava leaf extract possesses a potent inhibitory effect on PTP1B enzymatic activity and this PTP1B inhibition is through a slow oxidative but reversible inactivation on the enzyme. The reversible inactivation would suggest guava leaf extract may augment PTP1B inhibition alongside the endogenous H2O2 which itself is induced by insulin. In addition, our study confirmed the hypoglycemic efficacy being associated with guava leaf and found the most effective molecules reside in the aqueous partition which is also less cytotoxic to Chinese hamster ovary cells when compared to other less polar partitions. The guava leaf extract can modulate insulin activity through a redox regulation on PP1B enzymatic activity. It is speculated that a compound similar to gallocatechin in the aqueous partition can reduce an oxygen molecule to hydrogen peroxide which in turn oxidizes the catalytic residue Cys in PTP1B. Therefore, the guava leaf tea can serve as a functional hypoglycemic drink that is suitable for either healthy or diabetic subjects.展开更多
Paulownia tomentosa, P. fargesii, P. lamprorhylla, P. albiphloea, P. australis, P. fortunei, P. elongata, P. elongata f.alba and P. albiphloea var c henggtuensis were classified into three groups: P. fortunei group (...Paulownia tomentosa, P. fargesii, P. lamprorhylla, P. albiphloea, P. australis, P. fortunei, P. elongata, P. elongata f.alba and P. albiphloea var c henggtuensis were classified into three groups: P. fortunei group (P. fortunei a nd P. elongata f. alba); P. australis group (P. australis and P. albiphloea var chenggtuensis) and P. tomentasa group (P. tomentasa, P. fargesii, P. albiprhlaca , P. lamproprhylia and P. elongata ) accordance to the results of the single and two-dimensional SDS-PAGE of protein in the Paulownia tree leaves. The result co uld lay a foundation for classifying the Genus Paulownia plants.展开更多
文摘As an important agronomic trait, inclination of leaves is crucial Ior crop architecture and grain yields. 10 understand the molecular mechanism controlling rice leaf angles, one rice leaf inclination2 （1c2, three alleles） mutant was identified and functionally characterized. Compared to wild-type plants, lc2 mutants have enlarged leaf angles due to increased cell division in the adaxial epidermis of lamina joint. The LC2 gene was isolated through positional cloning, and encodes a vernalization insensitive 3-like protein. Complementary expression of LC2 reversed the enlarged leaf angles of lc2 plants, confirming its role in controlling leaf inclination. LC2 is mainly expressed in the lamina joint during leaf development, and particularly, is induced by the phytohormones abscisic acid, gibberellic acid, auxin, and brassinosteroids. LC2 is localized in the nucleus and defects of LC2 result in altered expression of cell division and hormone-responsive genes, indicating an important role of LC2 in regulating leaf inclination and mediating hormone effects.
基金financially supported by a grant from Tarbiat Modares University,Tehran,Iran
文摘The relationship between vernalization requirement and quantitative and qualitative changes in total leaf soluble proteins were determined in one spring （cv. Kohdasht） and two winter （cvs. Sardari and Norstar） cultivars of wheat （Triticum aestivum L.） exposed to 4℃. Plants were sampled on days 2, 14, 21 and 35 of exposure to 4℃. The final leaf number （FLN） was determined throughout the vernalization periods （0, 7, 14, 24, and 35 d） at 4℃. The final leaf number decreased until days 24 and 35 in Sardari and Norstar eultivars, respectively, indicating the vernalization saturation at these times. No clear changes were detected in the final leaf number of Kohdash cultivar, verifying no vernalization requirement for this spring wheat cultivar. Comparing with control, clear cold-induced 2-fold increases in proteins quantity occurred after 48 h following the 4℃-treatment in the leaves of the both winter wheat cultivars but, such response was not detected in the spring cultivar. However, the electrophoretic protein patterns showed between-cultivar and between-temperature treatment differences. With increasing exposure time to 4℃, the winter cultivars tended to produce more HMW polypeptides than the spring cultivar. Similar proteins were induced in both Sardari and Norstar winter wheat cultivars, however, the long vernalization requirement in Norstar resulted in high level and longer duration of expression of cold-induced proteins compared to Sardari with a short vernalization requirement. These observations indicate that vernalization response regulates the expression of low temperature （LT） tolerance proteins and determines the duration of expression of LT- induced proteins.
基金supported by the National Natural Science Foundation of China (30871578)the Key Project of National Plant Transgenic Genes of China(2008ZX08002004,2011ZX08002004)
文摘Proteomic assessment of low-abundance leaf proteins is hindered by the large quantity of ribulose-1,5-bisphosphate carboxylase/oxygenase （Rubisco） present within plant leaf tissues. In the present study, total proteins were extracted from wheat （Triticum aestivum L.） leaves by a conventional trichloroacetic acid （TCA）/acetone method and a protocol first developed in this work. Phytate/Ca2＋ fractionation and TCA/acetone precipitation were combined to design an improved TCA/acetone method. The extracted proteins were analysed by two-dimensional gel electrophoresis （2-DE）. The resulting 2-DE images were compared to reveal major differences. The results showed that large quantities of Rubisco were deleted from wheat leaf proteins prepared by the improved method. As many as （758±4） protein spots were detected from 2-DE images of protein extracts obtained by the improved method, 130 more than those detected by the TCA/acetone method. Further analysis indicated that more protein spots could be detected at regions of pI 4.00-4.99 and 6.50-7.00 in the improved method-based 2-DE images. Our findings indicated that the improved method is an efficient protein preparation protocol for separating low-abundance proteins in wheat leaf tissues by 2-DE analysis. The proposed protocol is simple, fast, inexpensive and also applicable to protein preparations of other plants.
基金Supported by National Natural Science Foundation of China(31472230)Natural Science Foundation of Hebei Province(C2014407068)Project of Hebei Department of Science and Technology(14966610D)
文摘[ Objective ] The paper was to explore effects of Echinacea polysaccharide （EPS） on expression of NF-KB protein secreted by LPS-injured IEC-6 cells, and to provide a theoretical basis for clinical application of Echinacea purpurea against bacterial diseases and enhancement of immunity. [ Method] Nucleoprotein extracted from IEC-6 cells in normal control group, LPS group, different concentrations of EPS （50, 100,200,500 μg/mL） ＋ LPS groups were detected by SDS- PAGE electrophoresis, and the content of NF-κB protein was analyzed using western blotting method. [ Result ] The content of NF-KB protein in normal control group was the lowest, while that in LPS group was the highest. The content of NF-κB protein in EPS group gradually decreased with the increasing concentration of EPS. [ Result] The expression of NF-κB protein increased when IEC-6 cells were stimulated by LPS, and EPS could effectively inhibit increased expression of NF- κB protein. With the increasing concentration of EPS, the inhibition effect against increased expression of NF-κB protein gradually strengthened.
文摘Sweet potato is one of the first natural GMOs, genetically modified 8000 years ago by Agrobacterium rhizogenes as reported recently by Kyndt et al. A section of 10 kbp long DNA (Transferred- DNA or T-DNA) of the Ri (Root-inducing) plasmid was transferred to the plant genome by A. rhizo-genes and has been maintained in all 291 hexaploid sweet potato cultivars of the world. The maintenance in the sweet potato genome and expression of two T-DNA genes for tryptophan-2-monooxygenease (iaaM) and for indole-3-acetamide hydrolase (iaaH) are likely to be physiologically significant since these enzymes convert tryptophan to indole-3-acetic acid, a major plant growth hormone auxin. Sweet potato (Ipomoea batatas (L.) Lam) is ranked the third most important root crop after potato and cassava, and the seventh in global food crop production with more than 126 million metric tons. Although sweet potato originated in Central or South America, China currently produces over 86% of world production with 109 million metric tons. In the United States, North Carolina is the leading producer with 38.5% of the 2007 sweet potato production, followed by California, Mississippi, and Louisiana with 23%, 19%, and 15.9%, respectively. Leaf curl virus diseases have been reported in sweet potato throughout the world. One of the causal agents is Sweet potato leaf curl virus (SPLCV) belonging to the genus Begomovirus (family Geminiviridae). Although SPLCV does not cause symptoms on Beauregard, one of the most predominant sweet potato cultivars in the US, it can reduce the yield up to 26%. Serological detection of SPLCV is not currently available due to the difficulties in obtaining purified virions that can be used as antigen for antiserum production. In attempts to obtain the coat protein (CP) of SPLCV for antibody production, primers were designed to amplify the CP gene. This gene was cloned into the expression vector pMAL-c2E as a fusion protein with maltose-binding protein, and transformed into Escherichia coli strain XL1-Blue. After gene induction, a fusion protein of 72 kDa was purified by amylose affinity chromatography. The yield of the purified fusion protein was approximately 200 μg/liter of bacterial culture. Digestion with enterokinase cleaved the fusion protein into a 42.5 kDa maltosebinding protein and a 29.4 kDa protein. The latter protein was identified by mass spectrometry analysis as the coat protein of SPLCV based on the fact that the mass spectrometry elucidated the sequences corresponding to 37% of amino acid positions of the SPLCV coat protein.
文摘Logistic and exponential approaches have been used to simulate plant growth and leaf area index (LAI) in different growing conditions. The objective of the present study was to develop and evaluate an approach to simulate maize LAI that expresses key physiological and phonological processes using a minimum entry requirement for Quality Protein maize (QPM) varieties grown in the southwestern region of the DR-Congo. Data for the development and testing of the model were collected manually in experimental plots using a non-destructive method. Simulation results revealed measurable variations between crop seasons (long season A and short season B) and between the two varieties (Mudishi-1 and Mudishi-3) for height, number of visible leaves, and LAI. For both seasons, Mudishi-3, a short stature variety was associated with expected stable yield based on simulation data. In general, the model simulated reliably all the parameters including the LAI. The LAI value for mudishi-1 was higher than that of Mudishi-3. There were significant differences among the model parameters (K, Ti, a, b, Tf) and between the two varieties. In all crop conditions studied and for the two varieties, the senescence rate (a) was higher, while the growth rate (b) was lower compared to the estimates based on the STICS model.
基金supported by the National Natural Science Foundation of China(31971902,32001509)China Agriculture Research System of MOF and MARA。
文摘The leaf is the main organ for rapeseed photosynthesis,and its morphology influences photosynthetic efficiency and supports increased planting density and yield.However,the molecular regulatory mechanism of leaf morphology in Brassica napus is poorly understood,restricting progress in breeding for the trait.We describe a novel dominant mutation,curly leaf 1(cl1),which confers uneven dorsal–ventral axis development,irregular cellular structure and influenced gravitropic response in the seedling stage.The CL1 locus was mapped to a 1.573-Mb interval on chromosome A05 using simple sequence repeat(SSR)markers,and co-segregated with the phenotype of plants in the curly F2 population.A substitution(P62S)was identified in the highly conserved degron motif(GWSPV)of the IAA2 protein in the cl1mutant,and the P62S substitution impaired the interaction between IAA2 and TIR1 in the presence of auxin,influencing auxin signaling.The P62S substitution-induced curly leaf phenotype was verified by ectopic expression of Bna A05.iaa2 in Arabidopsis and B.napus.Our findings explain the function of IAA2 in rapeseed,providing a foundation for future investigation of auxin signaling and the mechanisms underlying leaf development in B.napus.
基金This work was supported by Science-technology Support Foundation of Guizhou Province of China(No.[2019]2325,[2019]2308 and[2020]1Y125)National Natural Science Foundation of China(No.31870546)Forestry Department Foundation of Guizhou Province of China(No.[2017]14,[2018]13).
文摘According to the preparation method commonly used for soy proteinαbased adhesives,alfalfa leaf protein was used as the raw material to prepare alfalfa leaf protein-based wood adhesive.Differential scanning calorimetry analyzer(DSC),X-ray diffraction(XRD)and Fourier transform infrared spectroscopy(FTαIR)were used to characterize properties of the alfalfa leaf protein-based adhesive in this paper.The results revealed the following:(1)Chemical compositions and chemical structures of the alfalfa leaf protein were basically identical with those of the soy protein,both belonging to spherical proteins with the basis and potential for protein adhesives preparation,and spatial cross-linked network structures would be easily formed.(2)Alfalfa leaf protein and soy protein adhesives had the similar curing behaviors,curing temperature of alfalfa leaf protein-based adhesive was relaαtively lower,and the heating rate had minor influence on curing temperature of alfalfa leaf protein-based adhesive.At different heating rates,change tendencies of curing reaction degrees of both the two adhesives were not totally the same.(3)Activation energy and reaction frequency factor of the alfalfa leaf protein-based adhesive were higher than those of soy protein-based adhesive,indicating that the curing reaction of the alfalfa leaf protein adhesive was more difficult than soy protein-based adhesive,thus the dry shear strength and water resistance of alfalfa protein-based adhesive were lower than those of soy protein-based adhesive.Dynamics models of curing reactions of alfalfa leaf protein-based adhesive and soy protein-based adhesive are dα=dt/1.06×10^(13)e^(-97370/RT)(1-α)^(0.938) and dα/dt=1.09×10^(11)e^(-84260/RT) 1-α)^(0.928) respectively.The results of this study will expand the selection of raw materials for protein-based wood adhesives.
文摘4PU—30[N—phenyl—’N—(2—chloro—4—pyridyl) urea] is a new type of plant growth regulator with cytokinin properties. It has been confirmed to delay rice leaf senescence effectively. In order to elucidate the physiological role of 4PU—30 in delaying senescence, the changes of protein, nucleic acid contents, and the related activities of degradative enzymes were studied. Shanyou 63, an indica hybrid rice was used for this experiment. In the in vitro experiment, two full—developed leaves from the top during heading stage were collected and cut into 5.0cm segments, They were floated on the surface of distilled water containing 0.1mg/14PU—30 and incubated in darkness at 30 C. The leaves floated on distilled water were used as control.It was observed that chlorophyll content in controlled leaves declined rapidly started from the second day and dropped by 93.4% on the 6th day while that in leaves treated with 4PU—30 declined by 41.4% only. During senescence, specific activities of hemoglobin—digesting
文摘Guava leaf tea has been used as a folk medicine for treating hyperglycemic conditions in Asia and Africa. The hypoglycemic efficacy of guava leaf has been documented by many scientists in these regions, but the hypoglycemic mechanism is poorly understood. Guava leaves were extracted with methanol and the crude extract was partitioned against hexane, ethyl acetate, and butanol in sequence. The leftover in water is defined as the aqueous partition. A second smaller batch was extracted with hot water directly. Oral glucose tolerance test was carried out on healthy mice instead of diabetic mice that lack endogenous insulin. Glucose uptake was examined with 3T3-L1 adipocytes. Oxidative effect on PTP1B （protein tyrosine phosphatase 1b） was carried out with real-time PTP1B enzymatic assay. The aqueous partition of guava leaf extract possesses a potent inhibitory effect on PTP1B enzymatic activity and this PTP1B inhibition is through a slow oxidative but reversible inactivation on the enzyme. The reversible inactivation would suggest guava leaf extract may augment PTP1B inhibition alongside the endogenous H2O2 which itself is induced by insulin. In addition, our study confirmed the hypoglycemic efficacy being associated with guava leaf and found the most effective molecules reside in the aqueous partition which is also less cytotoxic to Chinese hamster ovary cells when compared to other less polar partitions. The guava leaf extract can modulate insulin activity through a redox regulation on PP1B enzymatic activity. It is speculated that a compound similar to gallocatechin in the aqueous partition can reduce an oxygen molecule to hydrogen peroxide which in turn oxidizes the catalytic residue Cys in PTP1B. Therefore, the guava leaf tea can serve as a functional hypoglycemic drink that is suitable for either healthy or diabetic subjects.
基金National Nature Science Foundation of China and Nature Science Foundation of Henan Province.
文摘Paulownia tomentosa, P. fargesii, P. lamprorhylla, P. albiphloea, P. australis, P. fortunei, P. elongata, P. elongata f.alba and P. albiphloea var c henggtuensis were classified into three groups: P. fortunei group (P. fortunei a nd P. elongata f. alba); P. australis group (P. australis and P. albiphloea var chenggtuensis) and P. tomentasa group (P. tomentasa, P. fargesii, P. albiprhlaca , P. lamproprhylia and P. elongata ) accordance to the results of the single and two-dimensional SDS-PAGE of protein in the Paulownia tree leaves. The result co uld lay a foundation for classifying the Genus Paulownia plants.
