2007Journal of Northwest A&F UniversityRequires access

Studies on protoplast fusion between strain of F46 and strain of SC1, SC11

Zong ZhaoFeng

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Abstract

The key factors affecting the protoplasts formation and fusants regeneration were determined between hyperparasitic Streptomyces F46 and actinomycetes SC1 or/and SCll. The results showed that the suitable concentration of Gly and sucrose for strain F46, SC1 and SCll were 0. 5 and 30 g/mL . The high rate of protoplasts formation and fusants regeneration could be obtained for strain F46 lysing 75 min with macerozyme of 10 mg/mL snailase and 10 mg/mL lysozyme (1:1) in 35℃water bath, and for strains SC1 and SC11 lysing respectively 60 min and 100 min with 10 mg/mL Lysozyme and 15 mg/mL lysozyme in 35℃water bath. The period of thermal inactivation in 55℃was 45 min for strain F46, and was 15 min for stain SC1 and SC11. The suitable inactivation period with UV light was respectively 16, 2 and 3 min for stain F46, SC1 and SC11.

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What this paper is about

The key factors affecting the protoplasts formation and fusants regeneration were determined between hyperparasitic Streptomyces F46 and actinomycetes SC1 or/and SCll. The results showed that the suitable concentration of Gly and sucrose for strain F46, SC1 and SCll were 0. 5 and 30 g/mL . The high rate of protoplasts formation and fusants regeneration could be obtained for strain F46 lysing 75 min with macerozyme of 10 mg/mL snailase and 10 mg/mL lysozyme (1:1) in 35℃water bath, and for strains SC1 and SC11 lysing respectively 60 min and 100 min with 10 mg/mL Lysozyme and 15 mg/mL lysozyme in 35℃water bath. The period of thermal inactivation in 55℃was 45 min for strain F46, and was 15 min for stain SC1 and SC11. The suitable inactivation period with UV light was respectively 16, 2 and 3 min for stain F46, SC1 and SC11.

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Available abstract

The key factors affecting the protoplasts formation and fusants regeneration were determined between hyperparasitic Streptomyces F46 and actinomycetes SC1 or/and SCll. The results showed that the suitable concentration of Gly and sucrose for strain F46, SC1 and SCll were 0. 5 and 30 g/mL . The high rate of protoplasts formation and fusants regeneration could be obtained for strain F46 lysing 75 min with macerozyme of 10 mg/mL snailase and 10 mg/mL lysozyme (1:1) in 35℃water bath, and for strains SC1 and SC11 lysing respectively 60 min and 100 min with 10 mg/mL Lysozyme and 15 mg/mL lysozyme in 35℃water bath. The period of thermal inactivation in 55℃was 45 min for strain F46, and was 15 min for stain SC1 and SC11. The suitable inactivation period with UV light was respectively 16, 2 and 3 min for stain F46, SC1 and SC11.

Key concepts: Protoplast, Lysozyme, Lysis, Strain (injury), Sucrose, Chemistry, Chromatography, Food science

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