Next-generation metabolic engineering approaches towards development of plant cell suspension cultures as specialized metabolite producing biofactories

被引:51
作者
Arya, Sagar S. [1 ,2 ]
Rookes, James E. [2 ]
Cahill, David M. [2 ]
Lenka, Sangram K. [1 ]
机构
[1] TERI Deakin Nano Biotechnol Ctr, Energy & Resources Inst, Gurugram 122001, Haryana, India
[2] Deakin Univ, Sch Life & Environm Sci, Waurn Ponds Campus, Geelong, Vic 3216, Australia
关键词
Plant cell suspension culture; Plant specialized metabolites; Plant gene clusters; Artificial gene cluster; Metabolic engineering; Computational modeling; GENE CLUSTERS; TRANSCRIPTOME ANALYSIS; SECONDARY METABOLITES; METHYL JASMONATE; NATURAL-PRODUCTS; CALLUS-CULTURES; DRUG-DELIVERY; SYNTHASE GENE; BABY-BOOM; BIOSYNTHESIS;
D O I
10.1016/j.biotechadv.2020.107635
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Plant cell suspension culture (PCSC) has emerged as a viable technology to produce plant specialized metabolites (PSM). While Taxol (R) and ginsenoside are two examples of successfully commercialized PCSC-derived PSM, widespread utilization of the PCSC platform has yet to be realized primarily due to a lack of understanding of the molecular genetics of PSM biosynthesis. Recent advances in computational, molecular and synthetic biology tools provide the opportunity to rapidly characterize and harness the specialized metabolic potential of plants. Here, we discuss the prospects of integrating computational modeling, artificial intelligence, and precision genome editing (CRISPR/Cas and its variants) toolboxes to discover the genetic regulators of PSM. We also explore how synthetic biology can be applied to develop metabolically optimized PSM-producing native and heterologous PCSC systems. Taken together, this review provides an interdisciplinary approach to realize and link the potential of next-generation computational and molecular tools to convert PCSC into commercially viable PSM-producing biofactories.
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页数:19
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