Zuñiga Cristal, Li Chien-Ting, Huelsman Tyler, Levering Jennifer, Zielinski Daniel C, McConnell Brian O, Long Christopher P, Knoshaug Eric P, Guarnieri Michael T, Antoniewicz Maciek R, Betenbaugh Michael J, Zengler Karsten
Department of Bioengineering, University of California, San Diego, La Jolla, California 92093-0412 (C.Z., T.H., J.L., D.C.Z., K.Z.);Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218 (C.-T.L., M.J.B.);Department of Chemical and Biomolecular Engineering, Metabolic Engineering and Systems Biology Laboratory, University of Delaware, Newark, Delaware 19716 (B.O.M., C.P.L., M.R.A.); andNational Bioenergy Center, National Renewable Energy Laboratory, Golden, Colorado 80401 (E.P.K., M.T.G.).
Department of Bioengineering, University of California, San Diego, La Jolla, California 92093-0412 (C.Z., T.H., J.L., D.C.Z., K.Z.);Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218 (C.-T.L., M.J.B.);Department of Chemical and Biomolecular Engineering, Metabolic Engineering and Systems Biology Laboratory, University of Delaware, Newark, Delaware 19716 (B.O.M., C.P.L., M.R.A.); andNational Bioenergy Center, National Renewable Energy Laboratory, Golden, Colorado 80401 (E.P.K., M.T.G.)
Plant Physiol. 2016 Sep;172(1):589-602. doi: 10.1104/pp.16.00593. Epub 2016 Jul 2.
The green microalga Chlorella vulgaris has been widely recognized as a promising candidate for biofuel production due to its ability to store high lipid content and its natural metabolic versatility. Compartmentalized genome-scale metabolic models constructed from genome sequences enable quantitative insight into the transport and metabolism of compounds within a target organism. These metabolic models have long been utilized to generate optimized design strategies for an improved production process. Here, we describe the reconstruction, validation, and application of a genome-scale metabolic model for C. vulgaris UTEX 395, iCZ843. The reconstruction represents the most comprehensive model for any eukaryotic photosynthetic organism to date, based on the genome size and number of genes in the reconstruction. The highly curated model accurately predicts phenotypes under photoautotrophic, heterotrophic, and mixotrophic conditions. The model was validated against experimental data and lays the foundation for model-driven strain design and medium alteration to improve yield. Calculated flux distributions under different trophic conditions show that a number of key pathways are affected by nitrogen starvation conditions, including central carbon metabolism and amino acid, nucleotide, and pigment biosynthetic pathways. Furthermore, model prediction of growth rates under various medium compositions and subsequent experimental validation showed an increased growth rate with the addition of tryptophan and methionine.
绿色微藻普通小球藻因其储存高脂质含量的能力及其天然的代谢多功能性,已被广泛认为是生物燃料生产的有前途的候选者。从基因组序列构建的区室化基因组规模代谢模型能够定量洞察目标生物体内化合物的运输和代谢。这些代谢模型长期以来一直被用于生成优化的设计策略以改进生产过程。在此,我们描述了普通小球藻UTEX 395的基因组规模代谢模型iCZ843的重建、验证及应用。基于重建中的基因组大小和基因数量,该重建代表了迄今为止任何真核光合生物最全面的模型。这个经过高度整理的模型能准确预测光合自养、异养和混合营养条件下的表型。该模型通过实验数据进行了验证,并为模型驱动的菌株设计和培养基改变以提高产量奠定了基础。不同营养条件下计算得到的通量分布表明,许多关键途径受氮饥饿条件影响,包括中心碳代谢以及氨基酸、核苷酸和色素生物合成途径。此外,对各种培养基组成下生长速率的模型预测及随后的实验验证表明,添加色氨酸和蛋氨酸后生长速率增加。