analysis of expression of all PLL genes in seedlings treated with hormones, abiotic stresses and elicitors of defense responses reveals significant changes in the expression of some PLLs without affecting the other PLLs
enzyme is detected in the late logarithmic growth phase, enzyme production is highest in the early stationary growth phase. The Alpine strain A15 produces high amounts of enzyme only at a cultivation temperature of 1-10°C, with a maximum of enzyme production at 5°C. Enzyme production by the Siberian strain AG25 is approximately twice as high than production by the Alpine strain A15
enzyme is detected in the late logarithmic growth phase, enzyme production is highest in the early stationary growth phase. The Siberian strain AG25 produces the enzyme over the growth temperature range of 1-20°C, with a maximum of enzyme production at 1°C. Enzyme production by the Siberian strain AG25 is approximately twice as high than production by the Alpine strain A15
the expression pattern of pectate lyase in Fragaria chiloensis reveal a gradual increment in the transcript level between stages 2 and 4, with a higher increment between stages 2 and 3 in Fragaria ananassa than in Fragaria chiloensis (stages 1 and 2 correspond to small, unripe and hard fruit, while stages 3 and 4 correspond to color-breaker and ripening fruit)
activity peak is observed on the 4th and 10th day of treatment with ethylene and 2,4-dichlorophenoxy acetic acid, respectively, compared to the 16th day in fruits not treated with phytohormone
activity peak is observed on the 4th and 10th day of treatment with ethylene and 2,4-dichlorophenoxy acetic acid, respectively, compared to the 16th day in fruits not treated with phytohormone
analysis of the expression pattern of all AtPLLs in different organs, at different stages of seedling development and in response to various hormones and stresses. The expression of PLLs varies considerably in different organs, with no expression of some PLLs in vegetative organs
pectate lyase production in Bacilli studied is modulated by the growth phase and by the carbon source present in the medium, low level expressionin Bacillus cereus
pectate lyase production in Bacilli studied is modulated by the growth phase and by the carbon source present in the medium, high level expression in Bacillus pumilus
pectate lyase production in Bacilli studied is modulated by the growth phase and by the carbon source present in the medium, high level expression in Bacillus subtilis
pectate lyase production in Bacilli studied is modulated by the growth phase and by the carbon source present in the medium. low level expressioni n Bacillus thuringiensis
analysis of the differential expression of pecCl1 during different stages of infectionby the phytopathgen shows a significant increase in pecCl1 expression five days after infection, at the onset of the necrotrophic phase
analysis of the differential expression of pecCl1 during different stages of infectionby the phytopathgen shows a significant increase in pecCl1 expression five days after infection, at the onset of the necrotrophic phase
transcripts of pectate lyase in the latex of rubber tree at various times after the first tapping is quantified by real-time PCR. Most transcripts are detected on the first day after tapping and then decreased with time
transcripts of pectate lyase in the latex of rubber tree at various times after the first tapping is quantified by real-time PCR. Most transcripts are detected on the first day after tapping and then decreased with time
pectate lyase production in Bacilli studied is modulated by the growth phase and by the carbon source present in the medium, high level expression in Bacillus fusiformis
pectate lyase production in Bacilli studied is modulated by the growth phase and by the carbon source present in the medium, low level expressionin Bacillus sphaericus
cell wall-modifying and aquaporin gene expression profiles follow similar trends in exocarp and mesocarp tissues throughout berry development, with the exception of the up-regulation of pectin methylesterase, pectate lyase, two aquaporin genes (AQ1 and AQ2), and two expansin genes (EXP3 and EXPL) during stage II, which is delayed in the exocarp tissue compared with mesocarp tissue
cell wall-modifying and aquaporin gene expression profiles follow similar trends in exocarp and mesocarp tissues throughout berry development, with the exception of the up-regulation of pectin methylesterase, pectate lyase, two aquaporin genes (AQ1 and AQ2), and two expansin genes (EXP3 and EXPL) during stage II, which is delayed in the exocarp tissue compared with mesocarp tissue