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In vitro culture of the tropical sponge Axinella corrugata (Demospongiae): Effect of food cell concentration on growth, clearance rate, and biosynthesis of stevensine

机译:热带海绵皱皮阿米氏菌的体外培养:食物细胞浓度对甜菊碱生长,清除率和生物合成的影响

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In vitro culture is one possible method for supplying sponge metabolites for pharmaceutical applications, but appropriate feeding regimens that maximize both growth and metabolite biosynthesis are largely unknown. According to the natural concentration (NC) of cells 1 to 50 mum in size that are available to wild Axinella corrugata, we fed explants a multispecific diet of bacteria, microalgae, and yeast at 4 different concentrations: 1NC, 3NC, 5NC, and 5+1NC (the last consisted of 5 NC of bacteria and 1NC of microalgae and yeast). Explants fed a 3NC diet had the best culture response, growing on average from 8.5 g to 10.3 g in 8 weeks, and showing a 110% increase in concentration (milligrams per gram of dry weight) of the antitumor compound stevensine. Stevensine production in 3NC explants, representing the total milligrams of metabolite per explant, increased by 157% over the study. Explants fed at 1NC had relatively stable weights, indicating that the diet met metabolic costs only. Explants fed at the two highest concentrations lost weight after 4 weeks, possibly because long-term high cell concentration blocked their aquiferous system, reducing their ability to feed efficiently. Stevensine production in explants fed the 1NC, 5NC, or 5+1NC diets were similar, and varied little from the initial amount. A separate experiment showed that the clearance rate for A. corrugata is similar between the examined food types and cell concentrations over 5 hours, averaging 766 ml h(-1) g DW-1. Overall, this study demonstrates that relatively small changes in food abundance can greatly affect both sponge growth and metabolite biosynthesis. The good growth and increased production of the target metabolite stevensine for A. corrugata explants fed a 3NC diet suggests that in vitro culture is a viable method of supplying some sponge metabolites.
机译:体外培养是为药物应用提供海绵代谢产物的一种可能方法,但是使生长和代谢产物生物合成均最大化的合适的饲喂方案仍然未知。根据野生野生瓦楞菌可获得的1至50微米大小的细胞的自然浓度(NC),我们以4种不同浓度的外植体喂养细菌,微藻类和酵母菌的多特异性饮食:1NC,3NC,5NC和5 + 1NC(最后一个由5 NC细菌以及1 NC微藻和酵母组成)。饲喂3NC饮食的植株具有最佳的培养反应,在8周内平均从8.5 g增长到10.3 g,并且抗肿瘤化合物甜菊糖的浓度(毫克/克干重)增加了110%。 3NC外植体中史蒂芬斯汀的产量代表每个外植体代谢产物的总毫克数,比该研究增加了157%。 1NC饲喂的植株具有相对稳定的体重,表明该饮食仅满足代谢成本。以两种最高浓度饲喂的外植体在4周后失去了体重,这可能是因为长期的高细胞浓度阻碍了其含水系统,从而降低了其有效饲喂的能力。饲喂1NC,5NC或5 + 1NC日粮的外植体中的史蒂文斯汀产量相似,与初始量相比变化很小。单独的实验表明,经过检查的食物类型和细胞浓度在5小时内对皱纹曲霉的清除率相似,平均为766 ml h(-1)g DW-1。总体而言,这项研究表明,食物丰度的相对较小变化会极大地影响海绵的生长和代谢产物的生物合成。饲喂3NC日粮的皱纹外植体目标代谢产物stevensine的良好生长和增加的产量表明,体外培养是提供一些海绵代谢产物的可行方法。

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