The Catalytic Role of RuBisCO for in situ CO 2 Recycling in Escherichia coli

• Published in: Frontiers in bioengineering and biotechnology 2020, Vol.8, p.543807
• Main Authors: Pang, Ju-Jiun, Shin, Jong-Shik, Li, Si-Yu
• Format: Article
• Language: English
• ISSN: 2296-4185; 2296-4185

Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) is a key enzyme responsible for biological CO assimilation. RuBisCO can be heterologously expressed in so that glucose and CO are co-metabolized to achieve high mixotrophic metabolite production, where the theoretical yield of mixotrophic metabolite production is 2.4 mol /mol . However, RuBisCO is known for its low k and for forming inhibited complexes with its substrate ribulose-1,5-bisphosphate (RuBP) and other sugar phosphates, yet the inhibited form of RuBisCO can be reversed by RuBisCO activase (Rca). In this study, RuBisCO forms I and II were cloned and expressed in for CO recycling, where CO produced during glucose fermentation was recycled and co-metabolized with the glucose. In addition, forms I and II RuBisCO activases were co-expressed with RuBisCO in to determine their effects on CO recycling. Form I RuBisCO activase (Rca1) was co-expressed with form I RuBisCO and form II RuBisCO activase (Rca2) was co-expressed with form II RuBisCO. The results showed that both form I and form II RuBisCO exhibit comparable activities in and generated similar levels of CO recycling. A significant increase in the total metabolite yield from 1.5 ± 0.1 to 2.2 ± 0.1 mol /mol occurred when Rca2 was co-expressed with form II RuBisCO. Meanwhile, the total metabolite yield increased from 1.7 ± 0.1 to 2.0 ± 0.1 mol /mol when Rca1 was co-expressed with form I RuBisCO. This data suggests that both forms I and II RuBisCO are subject to RuBP inhibition yet can be relieved by the co-expression of Rca. Interestingly, it is suggested that the RuBP inhibition of form II RuBisCO can be more easily reversed compared to form I. When the catalytic power of RuBisCO is maintained by Rca, the high activity of phosphoribulokinase (Prk) plays an important role in directing glucose to the RuBisCO-based engineered pathway and fermentation yields of 2.1-2.3 mol /mol can be obtained. This study is the first to demonstrate that RuBP inhibition of RuBisCO can be a bottleneck for CO recycling in .