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Cell Wall Regeneration around Protoplasts Isolated from Convolvulus Tissue Culture

机译:从旋花组织培养分离的原生质体周围的细胞壁再生

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摘要

Protoplasts of Convolvulus arvensis L. tissue culture regenerated a wall-like structure within 3 days in culture. Although unusually electron dense and atypically amorphous in the electron microscope, this structure could be digested with Myrothecium cellulase but was resistant to protease, a Rohm and Haas pectinase, and a β-1, 3-exoglucanase just like the original wall. A cytochemical test for callose was negative. Wall regeneration required a readily metabolized external carbon source and was not inhibited by a high concentration of cycloheximide, puromycin, or actinomycin D. Protoplast budding was correlated with the wall regeneration, and the latter was related quantitatively to the sucrose concentration in the medium. Although a concentration of 1 μm 2,4-dichlorophenoxy acetic acid is used normally for both general culture of the tissue and for wall regeneration, concentrations of 0 and 0.1 mm, which are highly deleterious to growth, have no appreciable effect on the incidence of the wall-like structure regenerated around protoplasts. The ability of protoplasts to undergo cell wall regeneration was decreased when they were cultured in the presence of proteolytic enzymes.
机译:旋花空心菜组织培养的原生质体在培养的三天内再生了壁状结构。尽管在电子显微镜下电子致密且非典型地为非晶态,但该结构可以用Myrothecium纤维素酶消化,但对蛋白酶,Rohm and Haas果胶酶和β-1、3-葡聚糖酶具有抵抗力,就像原始的壁一样。 call的细胞化学测试为阴性。壁再生需要一个易于代谢的外部碳源,并且不受高浓度的环己酰亚胺,嘌呤霉素或放线菌素D的抑制。原生质体出芽与壁再生相关,后者与培养基中蔗糖的浓度定量相关。尽管通常在组织的一般培养和壁再生中都使用浓度为1μm的2,4-二氯苯氧基乙酸,但是浓度0和0.1 mm对生长有很大的影响,但对组织的发生率没有明显的影响。壁状结构在原生质体周围再生。当它们在蛋白水解酶的存在下培养时,原生质体经历细胞壁再生的能力降低。

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