Kim Sarah M, Peña Matthew I, Moll Mark, Bennett George N, Kavraki Lydia E
Department of Computer Science, Rice University, 6100 Main St., Houston, TX, 77005, USA.
Department of BioSciences, Rice University, 6100 Main St., Houston, TX, 77005, USA.
J Cheminform. 2017 Sep 15;9(1):51. doi: 10.1186/s13321-017-0239-6.
Recent developments in metabolic engineering have led to the successful biosynthesis of valuable products, such as the precursor of the antimalarial compound, artemisinin, and opioid precursor, thebaine. Synthesizing these traditionally plant-derived compounds in genetically modified yeast cells introduces the possibility of significantly reducing the total time and resources required for their production, and in turn, allows these valuable compounds to become cheaper and more readily available. Most biosynthesis pathways used in metabolic engineering applications have been discovered manually, requiring a tedious search of existing literature and metabolic databases. However, the recent rapid development of available metabolic information has enabled the development of automated approaches for identifying novel pathways. Computer-assisted pathfinding has the potential to save biochemists time in the initial discovery steps of metabolic engineering. In this paper, we review the parameters and heuristics used to guide the search in recent pathfinding algorithms. These parameters and heuristics capture information on the metabolic network structure, compound structures, reaction features, and organism-specificity of pathways. No one metabolic pathfinding algorithm or search parameter stands out as the best to use broadly for solving the pathfinding problem, as each method and parameter has its own strengths and shortcomings. As assisted pathfinding approaches continue to become more sophisticated, the development of better methods for visualizing pathway results and integrating these results into existing metabolic engineering practices is also important for encouraging wider use of these pathfinding methods.
代谢工程领域的最新进展已成功实现了有价值产品的生物合成,例如抗疟化合物青蒿素的前体以及阿片类药物前体蒂巴因。在基因改造的酵母细胞中合成这些传统上来源于植物的化合物,使得大幅减少其生产所需的总时间和资源成为可能,进而让这些有价值的化合物变得更便宜且更容易获取。代谢工程应用中使用的大多数生物合成途径都是通过人工发现的,这需要对现有文献和代谢数据库进行繁琐的搜索。然而,随着可用代谢信息最近的快速发展,已能够开发出用于识别新途径的自动化方法。计算机辅助寻路有潜力在代谢工程的初始发现步骤中为生物化学家节省时间。在本文中,我们回顾了用于指导近期寻路算法搜索的参数和启发式方法。这些参数和启发式方法捕捉了有关代谢网络结构、化合物结构、反应特征以及途径的生物体特异性的信息。没有一种代谢寻路算法或搜索参数能脱颖而出成为广泛用于解决寻路问题的最佳选择,因为每种方法和参数都有其自身的优缺点。随着辅助寻路方法不断变得更加复杂,开发更好的方法来可视化途径结果并将这些结果整合到现有的代谢工程实践中,对于鼓励更广泛地使用这些寻路方法也很重要。