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培养的菠菜细胞原生质体愈伤组织的形成。

Callus formation from protoplasts of culturedSpinacia oleracea cells.

机构信息

Department of Agricultural Chemistry, Faculty of Horticulture, Chiba University, 640, Matsudo, Japan.

出版信息

Plant Cell Rep. 1985 May;4(3):148-50. doi: 10.1007/BF00571303.

Abstract

Cell suspensions were initiated from plumule derived calli ofSpinacia oleracea. Some of these cell lines could be maintained in culture for at least three years without a reduced growth rate. A high yield of protoplasts was obtained from the cell suspensions. When protoplasts were cultured in Murashige and Skoog medium with naphthaleneacetic acid and 6-benzyladenine, cell wall formation was observed after three days. The cultured protoplasts produced numerous cell-clusters within two weeks. However only protoplasts isolated from suspensions which were in a rapidly dividing phase were able to divide with a high frequency and give rise to callus colonies.

摘要

从菠菜幼芽衍生的愈伤组织中起始细胞悬浮液培养。其中一些细胞系可以在培养中至少维持三年而不降低生长速度。从细胞悬浮液中可以获得大量原生质体。当原生质体在含有萘乙酸和 6-苄基腺嘌呤的 Murashige 和 Skoog 培养基中培养时,在三天后观察到细胞壁形成。培养的原生质体在两周内产生了许多细胞簇。然而,只有那些来自快速分裂阶段的悬浮液分离的原生质体才能够以高频率分裂并产生愈伤组织集落。

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