Yang Jianming, Nie Qingjuan
Key Lab of Plant Biotechnology in Universities of Shandong Province; College of Life Sciences, Qingdao Agricultural University, Qingdao, 266109, China.
Key Lab of Applied Mycology, College of Life Sciences, Qingdao Agricultural University, No.700 Changcheng Road, Chengyang District, Qingdao, 266109, China.
Microb Cell Fact. 2016 May 5;15:74. doi: 10.1186/s12934-016-0475-x.
Under aerobic conditions, acetic acid is the major byproduct produced by E. coli during the fermentation. And acetic acid is detrimental to cell growth as it destroys transmembrane pH gradients. Hence, how to reduce the production of acetic acid and how to utilize it as a feedstock are of intriguing interest. In this study, we provided an evidence to produce β-caryophyllene by the engineered E. coli using acetic acid as the only carbon source.
Firstly, to construct the robust acetate-utilizing strain, acetyl-CoA synthases from three different sources were introduced and screened in the E. coli. Secondly, to establish the engineered strains converting acetic acid to β-caryophyllene, acetyl-CoA synthase (ACS), β-caryophyllene synthase (QHS1) and geranyl diphosphate synthase (GPPS2) were co-expressed in the E. coli cells. Thirdly, to further enhance β-caryophyllene production from acetic acid, the heterologous MVA pathway was introduced into the cells. What's more, acetoacetyl-CoA synthase (AACS) was also expressed in the cells to increase the precursor acetoacetyl-CoA and accordingly resulted in the increase of β-caryophyllene. The final genetically modified strain, YJM67, could accumulate the production of biomass and β-caryophyllene up to 12.6 and 1.05 g/L during 72 h, respectively, with a specific productivity of 1.15 mg h(-1) g(-1) dry cells, and the conversion efficiency of acetic acid to β-caryophyllene (gram to gram) reached 2.1%. The yield of β-caryophyllene on acetic acid of this strain also reached approximately 5.6% of the theoretical yield.
In the present study, a novel biosynthetic pathway for β-caryophyllene has been investigated by means of conversion of acetic acid to β-caryophyllene using an engineered Escherichia coli. This was the first successful attempt in β-caryophyllene production by E. coli using acetic acid as the only carbon source. Therefore, we have provided a new metabolic engineering tool for β-caryophyllene synthesis.
在有氧条件下,乙酸是大肠杆菌发酵过程中产生的主要副产物。并且乙酸对细胞生长有害,因为它会破坏跨膜pH梯度。因此,如何减少乙酸的产生以及如何将其用作原料具有极大的研究兴趣。在本研究中,我们提供了证据表明工程化大肠杆菌能够以乙酸作为唯一碳源生产β-石竹烯。
首先,为构建强大的乙酸利用菌株,将来自三种不同来源的乙酰辅酶A合成酶导入大肠杆菌并进行筛选。其次,为建立将乙酸转化为β-石竹烯的工程菌株,在大肠杆菌细胞中共表达乙酰辅酶A合成酶(ACS)、β-石竹烯合成酶(QHS1)和香叶基二磷酸合成酶(GPPS2)。第三,为进一步提高从乙酸生产β-石竹烯产量,将异源MVA途径导入细胞。此外,乙酰乙酰辅酶A合成酶(AACS)也在细胞中表达以增加前体乙酰乙酰辅酶A,从而导致β-石竹烯产量增加。最终的基因改造菌株YJM67在72小时内分别能够积累生物量和β-石竹烯产量至12.6 g/L和1.05 g/L,比生产率为1.15 mg h(-1) g(-1)干细胞,并且乙酸到β-石竹烯的转化效率(克对克)达到2.1%。该菌株乙酸上β-石竹烯的产量也达到理论产量的约5.6%。
在本研究中,通过利用工程化大肠杆菌将乙酸转化为β-石竹烯,研究了一种新的β-石竹烯生物合成途径。这是大肠杆菌以乙酸作为唯一碳源生产β-石竹烯的首次成功尝试。因此,我们为β-石竹烯合成提供了一种新的代谢工程工具。