菖蒲微繁培养基组成的改良。

Aida Wulansari, Tri Muji Ermayanti, Erwin Al Hafiizh, Betalini Widhi Hapsari, Evan Maulana
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引用次数: 0

摘要

在组织培养中,培养基成分的修改是找到最适合微繁的培养基配方的关键步骤。此外,减少一些营养物质以及糖和植物生长调节剂的浓度通常是使幼苗生产更经济的一种努力。本研究的目的是通过降低宏量营养素和糖浓度,结合BAP来改变菖蒲微繁培养基的组成。在MS培养基上,分别添加30、20、10 g/l的糖和0、0.5、1 mg/l的BAP,分别培养100、50、33.3、25%的宏量营养元素,建立菖蒲单株微繁殖试验。每个培养基处理有9个重复。每周测定培养物的生长情况,直到培养6周。记录的生长变量为芽数、叶长、叶数和根数。在培养6周时,还观察了叶绿素含量。结果表明:在MS培养基中,大量营养元素和糖的减少对苗数和叶数没有影响,但需要0.5 ~ 1 mg/l BAP;在不添加BAP的培养基中生根效果最好。在含有BAP的培养基中,所有常量营养素和糖浓度均降低,叶绿素含量降低。所有的幼苗都在地里存活了下来。减少大量营养元素和糖可用于菖蒲茎部培养。细胞分裂素BAP对芽的生长至关重要,但在生根过程中可以忽略。因此,这一发现为菖蒲低成本微繁提供了更多选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modification of media compositions for micropropagation of Acorus calamus L.
Modification of medium composition is a critical step in tissue culture to find out the best medium formulation for micropropagation. Furthermore, reduction of some nutrients as well as sugar and plant growth regulator concentrations are an effort often done to make the production of seedlings more economic. The aim of the study was to modify media composition by reduction of macronutrients and sugar concentrations in combination with BAP for micropropagation of Acorus calamus. Experiments of Calamus micropropagation was established by culturing single shoots to MS medium with 100, 50, 33.3 and 25% macronutrients added with sugar at 30, 20, and 10 g/l in combination with 0, 0.5, and 1 mg/l BAP. Each medium treatment had nine replicates. Growth of culture was determined every week until 6 weeks of culture. Growth variable recorded was shoots numbers, leaf length, leaf numbers and root numbers. At six weeks of culture, chlorophyll content was also observed. The results showed that reduction of macronutrients and sugar did not influence shoot and leaf numbers in MS medium but required 0.5-1 mg/l BAP. Rooting is best in medium with no addition of BAP. Chlorophyll content decreased in the medium containing BAP in all reduced macronutrients and sugar concentrations. All plantlets survived in the field. Reduction of macronutrients and sugar can be applied for Calamus shoot culture. Cytokinin BAP is critical for shoot growth but this could be omitted for rooting. Therefore, this finding offered more choices in micropropagation of Calamus with low-cost production.
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