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澳大利亚赫伦岛礁上的寻常海绵纲昆士兰双盘海绵的生物量组成分析。

Analysis of the biomass composition of the demosponge Amphimedon queenslandica on Heron Island Reef, Australia.

作者信息

Watson Jabin R, Brennan Timothy C R, Degnan Bernard M, Degnan Sandie M, Krömer Jens O

机构信息

School of Biological Science, University of Queensland, Brisbane, Queensland 4072, Australia.

Systems and Synthetic Biology Group, Australian Institute for Bioengineering and Nanotechnology, University of Queensland, Brisbane, Queensland 4072, Australia.

出版信息

Mar Drugs. 2014 Jun 23;12(6):3733-53. doi: 10.3390/md12063733.

Abstract

Marine sponges are a potential source of important pharmaceutical drugs, the commercialisation of which is restricted by the difficulties of obtaining a sufficient and regular supply of biomass. One way to optimize commercial cell lines for production is the in-depth characterization and target identification through genome scale metabolic modeling and flux analysis. By applying these tools to a sponge, we hope to gain insights into how biomass is formed. We chose Amphimedon queenslandica as it has an assembled and annotated genome, a prerequisite for genome scale modeling. The first stepping stone on the way to metabolic flux analysis in a sponge holobiont, is the characterization of its biomass composition. In this study we quantified the macromolecular composition and investigated the variation between and within sponges of a single population. We found lipids and protein to be the most abundant macromolecules, while carbohydrates were the most variable. We also analysed the composition and abundance of the fatty acids and amino acids, the important building blocks required to synthesise the abundant macromolecule types, lipids, and protein. These data complement the extensive genomic information available for A. queenslandica and lay the basis for genome scale modelling and flux analysis.

摘要

海洋海绵是重要药物的潜在来源,但其商业化受到难以获得充足且稳定的生物量供应的限制。优化用于生产的商业细胞系的一种方法是通过基因组规模代谢建模和通量分析进行深入表征和靶点识别。通过将这些工具应用于海绵,我们希望深入了解生物量是如何形成的。我们选择了昆士兰扁海绵,因为它有一个已组装和注释的基因组,这是基因组规模建模的先决条件。在海绵共生体中进行代谢通量分析的第一步,是表征其生物量组成。在本研究中,我们对大分子组成进行了量化,并研究了单个种群内海绵之间以及海绵内部的差异。我们发现脂质和蛋白质是最丰富的大分子,而碳水化合物的变化最大。我们还分析了脂肪酸和氨基酸的组成及丰度,它们是合成丰富的大分子类型(脂质和蛋白质)所需的重要组成部分。这些数据补充了昆士兰扁海绵现有的大量基因组信息,并为基因组规模建模和通量分析奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a0/4071599/8e583497dbb4/marinedrugs-12-03733-g001.jpg

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