gene ATHCOR1: construction of transgenic Arabidopsis thaliana plants overexpressing the enzyme via infection with Agrobacterium tumefaciens and transformation, sense and antisense orientation, the sense mutation changed the chlorophyll a to chlorophyll b ratio, overview, gene AtCLH2: cloning and analysis
construction of T-DNA insertion clh1 and clh2 single and double knockout lines, which are still able to degrade chlorophyll during senescence, phenotypes, overview
construction of T-DNA insertion clh1 and clh2 single and double knockout lines, which are still able to degrade chlorophyll during senescence, phenotypes, overview
construction of T-DNA insertion clh1 and clh2 single and double knockout lines, which are still able to degrade chlorophyll during senescence, phenotypes, overview
inhibition of expression of AtCLH2 by RNA interference, transfection using Agrobacterium tumefaciens strain LBA4404, AtCLH2 RNAi plants show decreased contents of chlorophyllide without a substantial change in the total amount of the extractable chlorophyll and consequently presented lower chlorophyllide to chlorophyll ratios in their leaves, phenotype, overview
construction of clh1 and clh1/clh2 mutant plants as transfer DNA insertion lines. Methyl jasmonate promotes chlorophyll degradation in the clh mutants as well as in the wild-type, phenotypes, overview
construction of clh1 and clh1/clh2 mutant plants as transfer DNA insertion lines. Methyl jasmonate promotes chlorophyll degradation in the clh mutants as well as in the wild-type, phenotypes, overview
development of micellar electrokinetic chromatography (MEKC) assay for the plant membrane enzyme chlorophyllase, evaluation of several different permanently and dynamically coated capillaries
construction of clh1 and clh1/clh2 mutant plants as transfer DNA insertion lines. Methyl jasmonate promotes chlorophyll degradation in the clh mutants as well as in the wild-type, phenotypes, overview
a chimeric construct with the antisense gene BoCLH1, driven by the CaMV 35S promoter and Nos-terminator and harboring the hygromycin resistance gene, is used for Agrobacterium tumefaciens-mediated transformation, effects of the antisense BoCLH1 gene on the postharvest senescence of broccoli, phenotype with slower postharvest yellowing during storage in the dark at 20°C, overview
a chimeric construct with the antisense gene BoCLH1, driven by the CaMV 35S promoter and Nos-terminator and harboring the hygromycin resistance gene, is used for Agrobacterium tumefaciens-mediated transformation, effects of the antisense BoCLH1 gene on the postharvest senescence of broccoli, phenotype with slower postharvest yellowing during storage in the dark at 20°C, overview
a chimeric construct with the antisense gene BoCLH1, driven by the CaMV 35S promoter and Nos-terminator and harboring the hygromycin resistance gene, is used for Agrobacterium tumefaciens-mediated transformation, effects of the antisense BoCLH1 gene on the postharvest senescence of broccoli, phenotype with slower postharvest yellowing during storage in the dark at 20°C, overview
usage of a polystyrene divinylbenzene-based metal chelator to purify and immobilize recombinant poly(His)-tagged recombinant BoCLH1. Cu2+ exhibits the highest capacity and purification efficiency, therefore DIAION®CR11Cu(II) is the preferred resin for enzyme immobilization. Enzyme immobilized on His-Trap resin is about 2fold stabilized at 60°C and during 17 cycles of use compared to free enzyme. Enzyme immobilized on resin is about 2fold stabilized at 60°C and during 17 cycles of use compared to free enzyme
usage of a polystyrene divinylbenzene-based metal chelator to purify and immobilize recombinant poly(His)-tagged recombinant BoCLH1. Cu2+ exhibits the highest capacity and purification efficiency, therefore DIAION®CR11Cu(II) is the preferred resin for enzyme immobilization. Enzyme immobilized on His-Trap resin is about 2fold stabilized at 60°C and during 17 cycles of use compared to free enzyme. Enzyme immobilized on resin is about 2fold stabilized at 60°C and during 17 cycles of use compared to free enzyme
expression of full-length citrus Chlase results in limited chlorophyll breakdown in tobacco protoplasts and no visible leaf phenotype in whole plants, whereas expression of a Chlase version lacking the N-terminal 21 amino acids, i.e. ChlaseDELTAN, which corresponds to the mature protein, leads to extensive chlorophyll breakdown in both tobacco protoplasts and squash leaves, mutant ChlaseDELTAN-expressing squash leaves display a dramatic chlorotic phenotype in plants grown under low-intensity light, whereas under natural light a lesion-mimic phenotype occurrs, which follows the accumulation of chlorophyllide, a photodynamic chlorophyll breakdown product, phenotypes, overview
entrapping of the enzyme in tetramethoxysilane-based sol-gel in the presence of lipid, acetone is used to introduce the substrate-chlorophyll into aqueous reaction medium in solubilized form, the entrapped chlorophyllase is less sensitive toward the denaturing effect of acetone in the bulk phase than the free enzyme, sol-gel at wet-stage, diffusion coefficient and partition coefficient of chlorophyll in sol-gel, overview
optimization of chlorophyllase-catalyzed hydrolysis of chlorophyll in monophasic organic solvent media, best in a mixture of hexane/2-octanone of 98.3:1.7 v/v, overview