Nuclease p1 produced by Penicillium citrinum was purified and characterized. Fermentation was carried out for 49 h for optimum production.
The enzyme was purified to homogeneity according to SDS-PAGE by thermal deactivation, ultrafiltration, (NH4)2SO4 precipitation, phenyl
sepharose chromatography, ion-exchange chromatography and gel filtration. This protocol improved 93-fold purification and 5.4% recovery of
enzyme activity. The molecular mass of nuclease p1 from Penicillium citrinum was estimated to be in the range from 43 to 44 kDa. The enzyme
showed an obligate requirement for Zn2+ for activity. K+ had a significant effect on enzyme activity. Mg2+ and Ca2+ had a slight positive effect on
enzyme activity. While Cu2+, Co2+, Al3+, SDS and Triton X-100 were strong inhibitors of nuclease p1. The enzyme was completely stable in the pH
range from 5 to 6.5 and had a pH optimum of 5.4. The optimum temperature of nuclease p1 was 69 8C and enzyme was stable up to 70 8C. Km and
Vmax for the purified enzyme were 24.28 mg/ml and 0.36 mg/ml min, respectively, with RNA as substrate.
Nuclease p1 produced by Penicillium citrinum was purified and characterized. Fermentation was carried out for 49 h for optimum production.The enzyme was purified to homogeneity according to SDS-PAGE by thermal deactivation, ultrafiltration, (NH4)2SO4 precipitation, phenylsepharose chromatography, ion-exchange chromatography and gel filtration. This protocol improved 93-fold purification and 5.4% recovery ofenzyme activity. The molecular mass of nuclease p1 from Penicillium citrinum was estimated to be in the range from 43 to 44 kDa. The enzymeshowed an obligate requirement for Zn2+ for activity. K+ had a significant effect on enzyme activity. Mg2+ and Ca2+ had a slight positive effect onenzyme activity. While Cu2+, Co2+, Al3+, SDS and Triton X-100 were strong inhibitors of nuclease p1. The enzyme was completely stable in the pHrange from 5 to 6.5 and had a pH optimum of 5.4. The optimum temperature of nuclease p1 was 69 8C and enzyme was stable up to 70 8C. Km andVmax for the purified enzyme were 24.28 mg/ml and 0.36 mg/ml min, respectively, with RNA as substrate.
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Nuclease p1 produced by Penicillium citrinum was purified and characterized. Fermentation was carried out for 49 h for optimum production.
The enzyme was purified to homogeneity according to SDS-PAGE by thermal deactivation, ultrafiltration, (NH4)2SO4 precipitation, phenyl
sepharose chromatography, ion-exchange chromatography and gel filtration. This protocol improved 93-fold purification and 5.4% recovery of
enzyme activity. The molecular mass of nuclease p1 from Penicillium citrinum was estimated to be in the range from 43 to 44 kDa. The enzyme
showed an obligate requirement for Zn2 for activity. K had a significant effect on enzyme activity. Mg2 and Ca2 had a slight positive effect on
enzyme activity. While Cu2 , Co2 , Al3 ,SDS และ Triton X-100 ยับยั้งแรงของนิวเคลียส P1 . เอนไซม์มีเสถียรภาพอย่างสมบูรณ์ในช่วง pH
5 - 6.5 และมี pH ที่เหมาะสมของ 5.4 . อุณหภูมิที่เหมาะสมของนิวเคลียส P1 คือ 69 8C และ เอนไซม์ขึ้น 70 8C . km และ
Vmax สำหรับเอนไซม์คือ 24.28 mg / ml และ 0.36 มิลลิกรัม / มิลลิลิตรต่อนาที ตามลำดับ มี RNA เป็นสับสเตรท
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