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Production and regeneration of protoplasts from Grateloupia turuturu Yamada (Rhodophyta)

机译:山齿Grateloupia turuturu Yamada(Rhodophyta)原生质体的产生和再生

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摘要

Protoplasts were isolated enzymatically from the carrageenophyte red alga Grateloupia turuturu (Halymeniales, Rhodophyta) that occurs along the coast of the French Channel in Normandy. Effects of the main factors on the protoplast yield were identified to improve the isolation protocol. The optimal enzyme composition for cell wall digestion and protoplast viability consisted of 2% cellulase Onozuka R-10, 0.5% macerozyme R-10, 2% crude extract from viscera of Haliotis tuberculata, 0.8 M mannitol, 20 mM sodium citrate, 0.3% bovine serum albumin at 25°C, and 4-h incubation period. The protoplasts were approximately 5–15 μm in diameter, liberated mainly from the surface cell layers. Maximum yield was 1.5 × 107 protoplasts g-1 fresh tissue. The protoplasts underwent initial division after 14 days with a high density level of 1 × 106 cells mL-1 in culture medium and developed into microthalli of a line of two to six cells.
机译:原生质体是通过酶法从诺曼底法国海峡沿岸的角叉菜藻红藻Grateloupia turuturu(Halymeniales,Rhodophyta)中分离出来的。确定主要因素对原生质体产量的影响,以改善分离方案。用于细胞壁消化和原生质体生存力的最佳酶组成包括2%纤维素酶Onozuka R-10、0.5%宏核酶R-10、2%Haliotis tuberculata内脏的粗提物,0.8 M甘露醇,20 mM柠檬酸钠,0.3%牛血清白蛋白在25°C下孵育4小时。原生质体的直径约为5–15μm,主要从表面细胞层释放出来。最大产量为1.5×10 7 原生质体g -1 新鲜组织。 14天后,原生质体在培养基中以1×10 6 细胞mL -1 的高密度水平进行初次分裂,并发育成2到6行的微丘脑细胞。

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