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Researchers at the University of Manchester say they have made a breakthrough in the development of synthetic pathways that will allow the renewable biosynthesis of propane. This discovery brings scientists closer to developing renewable propane.
The University of Manchester scientists say propane has good physiochemical properties that allow it to be stored and transported in a compressed liquid form. Under ambient conditions, propane serves as a clean-burning gas, which makes it an attractive target to become a renewable alternative to petroleum.
While natural metabolic pathways for the renewable biosynthesis of propane do not exist, scientists at the University of Manchester developed an alternative microbial biosynthetic pathway to produce renewable propane. The University of Manchester team modified existing fermentative butanol pathways using an engineered enzyme variant to redirect the microbial pathway to produce propane as opposed to butanol. The team was able to achieve propane biosynthesis, creating a platform for next-generation microbial propane production.
Propane (C3H8) is a volatile hydrocarbon with highly favourable physicochemical properties as a fuel, in addition to existing global markets and infrastructure for storage, distribution and utilization in a wide range of applications. Consequently, propane is an attractive target product in research aimed at developing new renewable alternatives to complement currently used petroleum-derived fuels. This study focuses on the construction and evaluation of alternative microbial biosynthetic pathways for the production of renewable propane. The new pathways utilize CoA intermediates that are derived from clostridial-like fermentative butanol pathways and are therefore distinct from the first microbial propane pathways recently engineered in Escherichia coli.
Results
We report the assembly and evaluation of four different synthetic pathways for the production of propane and butanol,
Conclusions
This study expands the metabolic toolbox for renewable propane production and provides new insight and understanding for the development of next-generation biofuel platforms. In developing an alternative CoA-dependent fermentative butanol pathway, which includes an engineered ADO variant (ADOA134F), the study addresses known limitations, including the low bio-availability of butyraldehyde precursors and poor activity of ADO with butyraldehyde.
Keywords: Propane; Butanol; Microbial pathway engineering; Cyanobacteria; Aldehyde deformylating oxygenase; Escherchia coli
A microbial platform for renewable propane synthesis based on a fermentative butanol pathway
Background
Propane, a major component of autogas or liquefied petroleum gas (LPG), is an emerging fuel for future energy supply and transportation [1]. Propane is the third most widely used motor fuel and about 20 million tonnes of propane gas are used per year to fuel motor vehicles [2]. It is estimated that propane provides heat and energy for more than 14 million homes worldwide annually [3],[4]. Propane also has an existing global market for a wide number of other stationary and mobile applications, such as low emission vehicles, gas burners and refrigeration systems [5]. Easy separation from liquid biotechnological processes as a gas and less energy requirements for liquefaction and storage offers potential advantages to propane over other gaseous fuels [6].
Natural metabolic pathways for the renewable biosynthesis of propane do not exist. The discovery of an aldehyde deformylating oxygenase (ADO) from cyanobacteria, however, has paved the way for synthetic alkane pathways to be constructed [7]-[9]. A microbial platform for propane generation dependent on fatty acid biosynthesis was recently reported [10]. The authors concluded that the pathway was limited by total flux through fatty acid synthesis (FAS). The most obvious example of this limitation comes from the markedly enhanced rate of propane synthesis observed when fatty acids were supplied to the external media. In the present study, we sought to bypass this limitation by generating new synthetic pathways that are not dependent on FAS. In this study, we designed a series of modified butyraldehyde pathways based on the CoA-dependent butanol pathways commonly found in Clostridium spp. Propane biosynthesis was thereafter achieved by interrupting the route to alcohol by the addition of ADO (Figure 1).
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