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由日本桤木叶片原生质体再生小植株。

Plantlet regeneration from mesophyll protoplasts ofBetula platyphylla var.japonica.

机构信息

Forestry and Forest Products, Department of Forest Science, Faculty of Agriculture, Utsunomiya University, Utsunomiya 321, Tochigi, Japan.

出版信息

Plant Cell Rep. 1996 Nov;16(1-2):50-3. doi: 10.1007/BF01275448.

Abstract

InBetula platyphylla var.japonica, colonies were induced efficiently from mesophyll protoplasts cultured in half strength MS (1/2MS) liquid medium containing 0.6 M mannitol, 0.09M sucrose and 1 μM 4-PU and 1 μM NAA at a cell density of 5 × 10(4)/ml. The colonies grew actively and developed into callus after 3 months of culture.Roots differentiated from the protoplast-derived white calluses cultured on the 1 /2MS solid media supplemented with 0.1-1 μM 4-PU and 1 μM NAA, and 10 μM zeatin with no supplementation of NAA. Furthermore, the protoplast-derived green callus differentiated shoots with 1/2MS solid medium containing 1 μM 4-PU or 10 μM zeatin with no supplementation of NAA. When shoots obtained were cultured on the cytokinin-free MS solid medium with 2.5 μM IBA and 0.1 μM NAA, they rooted and developed into plantlets after one month of culture.The phenylurea-type cytokinin, 4-PU, was effective for plantlet regeneration from the mesophyll protoplasts ofB. platyphylla var.japonica. This suggests that there is potential for the use of 4-PU in the culture of protoplasts in many forest tree species.

摘要

在银桦杂种中,从叶肉原生质体培养在含有 0.6 M 甘露醇、0.09 M 蔗糖和 1 μM 4-PU 和 1 μM NAA 的半强度 MS(1/2MS)液体培养基中,以 5×10(4)/ml 的细胞密度,有效地诱导了集落。在补充有 0.1-1 μM 4-PU 和 1 μM NAA、10 μM 玉米素且不补充 NAA 的 1/2MS 固体培养基上,原胚衍生的白色愈伤组织分化出根。此外,原胚衍生的绿色愈伤组织在含有 1 μM 4-PU 或 10 μM 玉米素且不补充 NAA 的 1/2MS 固体培养基上分化出芽。当获得的芽在不含细胞分裂素的 MS 固体培养基上培养,含有 2.5 μM IBA 和 0.1 μM NAA 时,它们在一个月的培养后生根并发育成小植株。苯脲型细胞分裂素 4-PU 对银桦杂种叶肉原生质体的植株再生有效。这表明 4-PU 在许多林木树种的原生质体培养中有应用潜力。

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