fter the alcoholic group of serine located in the binding site of Anti-HumanIgM(Fcμ) (Rabbit IgG) was selectively activated by phenylmethylsulfonyl fluoride(PMSF) and displaced with hydrogen selenide(H2Se) , the seri...fter the alcoholic group of serine located in the binding site of Anti-HumanIgM(Fcμ) (Rabbit IgG) was selectively activated by phenylmethylsulfonyl fluoride(PMSF) and displaced with hydrogen selenide(H2Se) , the serine residue was con-verted to selenocysteine(SeCys). Because SeCys is a catalytic group of glutathioneperoxidase (GPX), the mutated antibody has the GPX activity which is seventytimes more than that of PZ51, the best GPX mimic in the world. Moreover, themutated antibody remains its original antibody titer.展开更多
Penicillium simplicissimum was cultured and preserved on the potato dextrose agar(PDA)medium.PDA-RBBR(Remazal Brilliant Blue R)medium was used for the screening of the strains,which is able to produce enzymes.After th...Penicillium simplicissimum was cultured and preserved on the potato dextrose agar(PDA)medium.PDA-RBBR(Remazal Brilliant Blue R)medium was used for the screening of the strains,which is able to produce enzymes.After the mutation process in Penicillium simplicissimum induced by chemical reagent and ultraviolet radiation,a high laccase-producing strains Penicillium simplicissimum was obtained.When 5 m L diethyl sulfate(2%)was mixed along with 5 m L spore suspension for 30 min,chemical mutagenesis reached its best condition.And the optimum conditions of UV mutagenesis were that spore suspension was irradiated for 4 min under 15 W UV lamp at a distance of 30 cm.The highest activity of C_5E_4 strains was 4.80 U/g over 18%higher than the maximum laccase activity of original microorganism.Five generations of the mutant strains were cultured,and the laccase activity of the strains was measured.The result showed that C_5E_4 strains can product laccase of the five subcultures stably.展开更多
Mutagenized populations have provided important materials for introducing variation and identifying gene function in plants. In this study, an ethyl methanesulfonate（EMS）-induced soybean（Glycine max） population,co...Mutagenized populations have provided important materials for introducing variation and identifying gene function in plants. In this study, an ethyl methanesulfonate（EMS）-induced soybean（Glycine max） population,consisting of 21,600 independent M_2 lines, was developed.Over 1,000 M_（4（5））families, with diverse abnormal phenotypes for seed composition, seed shape, plant morphology and maturity that are stably expressed across different environments and generations were identified. Phenotypic analysis of the population led to the identification of a yellow pigmentation mutant, gyl, that displayed significantly decreased chlorophyll（Chl） content and abnormal chloroplast development. Sequence analysis showed that gyl is allelic to Minn Gold, where a different single nucleotide polymorphism variation in the Mg-chelatase subunit gene（ChlI1a） results in golden yellow leaves. A cleaved amplified polymorphic sequence marker was developed and may be applied to marker-assisted selection for the golden yellow phenotype in soybean breeding. We show that the newly developed soybean EMS mutant population has potential for functional genomics research and genetic improvement in soybean.展开更多
文摘fter the alcoholic group of serine located in the binding site of Anti-HumanIgM(Fcμ) (Rabbit IgG) was selectively activated by phenylmethylsulfonyl fluoride(PMSF) and displaced with hydrogen selenide(H2Se) , the serine residue was con-verted to selenocysteine(SeCys). Because SeCys is a catalytic group of glutathioneperoxidase (GPX), the mutated antibody has the GPX activity which is seventytimes more than that of PZ51, the best GPX mimic in the world. Moreover, themutated antibody remains its original antibody titer.
基金Projects(51178172,51308076,51408206,51578222)supported by the National Natural Science Foundation of ChinaProject(113049A)supported by the Ministry of Education of China
文摘Penicillium simplicissimum was cultured and preserved on the potato dextrose agar(PDA)medium.PDA-RBBR(Remazal Brilliant Blue R)medium was used for the screening of the strains,which is able to produce enzymes.After the mutation process in Penicillium simplicissimum induced by chemical reagent and ultraviolet radiation,a high laccase-producing strains Penicillium simplicissimum was obtained.When 5 m L diethyl sulfate(2%)was mixed along with 5 m L spore suspension for 30 min,chemical mutagenesis reached its best condition.And the optimum conditions of UV mutagenesis were that spore suspension was irradiated for 4 min under 15 W UV lamp at a distance of 30 cm.The highest activity of C_5E_4 strains was 4.80 U/g over 18%higher than the maximum laccase activity of original microorganism.Five generations of the mutant strains were cultured,and the laccase activity of the strains was measured.The result showed that C_5E_4 strains can product laccase of the five subcultures stably.
基金supported by National Key R&D Program for Crop Breeding (2016YFD0100201)the Crop Germplasm Resources Protection (2014NWB030, 2015NWB030-05)+1 种基金Platform of National Crop Germplasm Resources of China (2014-004, 2015-004)The Agricultural Science and Technology Innovation Program of the Chinese Academy of Agricultural Sciences (CAAS)
文摘Mutagenized populations have provided important materials for introducing variation and identifying gene function in plants. In this study, an ethyl methanesulfonate（EMS）-induced soybean（Glycine max） population,consisting of 21,600 independent M_2 lines, was developed.Over 1,000 M_（4（5））families, with diverse abnormal phenotypes for seed composition, seed shape, plant morphology and maturity that are stably expressed across different environments and generations were identified. Phenotypic analysis of the population led to the identification of a yellow pigmentation mutant, gyl, that displayed significantly decreased chlorophyll（Chl） content and abnormal chloroplast development. Sequence analysis showed that gyl is allelic to Minn Gold, where a different single nucleotide polymorphism variation in the Mg-chelatase subunit gene（ChlI1a） results in golden yellow leaves. A cleaved amplified polymorphic sequence marker was developed and may be applied to marker-assisted selection for the golden yellow phenotype in soybean breeding. We show that the newly developed soybean EMS mutant population has potential for functional genomics research and genetic improvement in soybean.
