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Assessment of Acid Phosphatase Production by In vitro Cultures of Atropa acuminata

机译:Atropa acuminata体外培养评估酸性磷酸酶的能力

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The potential of various culture lines of Atropa acuminata were investigated for resourcing acid phosphatase (ACP) (3.1.3.2). Crude enzyme extract comprised of a mixture of four isoforms, distinguishable by polyacrylamide gel electrophoresis (PAGE) with molecular weight ranging from 39 to 215 kDa. In vitro regenerated proliferative shoots, callus and roots showed higher specific activity (2.49, 3.41, 2.91 U/mg protein, respectively) as compared to in vivo grown plants (0.71 U/mg protein). ACP activity in root cultures increased progressively up to 4.6 U/mg during the entire growth period (2 ‐ 24 weeks), whereas in case of shoot cultures, the specific activity escalated to 2.49 U/mg at 8 weeks, which then declined subsequently (1.95 U/mg). Similarly, callus cultures initially showed a higher phosphohydrolytic activity (3.41 U/mg protein) until 8 weeks by which period, it decreased with the passage of growth period. The present studies reveal an alternate system for resourcing of ACP from Atropa acuminata.Plant Tissue Cult. & Biotech. 26(1): 15-23, 2016 (June)
机译:研究了Atropa acuminata的各种培养品系对酸性磷酸酶(ACP)的恢复潜力(3.1.3.2)。粗制酶提取物,由四种同工型的混合物组成,可通过聚丙烯酰胺凝胶电泳(PAGE)进行区分,分子量范围为39至215 kDa。与体内生长的植物(0.71 U / mg蛋白质)相比,体外再生的增殖芽,愈伤组织和根显示出更高的比活性(分别为2.49、3.41、2.91 U / mg蛋白质)。在整个生长期(2-24周)内,根培养物中的ACP活性逐渐增加至4.6 U / mg,而在芽培养的情况下,比活性在8周时升至2.49 U / mg,随后下降( 1.95 U / mg)。同样,愈伤组织培养物最初显示较高的磷酸水解活性(3.41 U / mg蛋白),直到8周为止,随着生长期的增长而降低。本研究揭示了一种替代系统,可从Atropa acuminata获得ACP。植物组织培养。和生物技术。 26(1):2016年6月15日至23日

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