Bao Jie, Ryu Dewey D Y
Biochemical Engineering Program, University of California, One Shields Ave, Davis, California 95616, USA.
Biotechnol Bioeng. 2007 Sep 1;98(1):1-11. doi: 10.1002/bit.21498.
Polymerase chain reaction (PCR) and other PCR applications for DNA synthesis require deoxynucleoside triphosphates (dNTP) as the essential precursors and substrates. Currently, the dNTP is commercially produced by a chemical method which is environmentally hazardous and costly due to its low yields in both the synthetic reaction and purification processes. In this study, a enzyme technology for the total integrated biosynthesis of all dNTP components is presented. The bioprocess technology developed and reported here involves two sequential enzymatic phosphorylation reactions coupled with the cofactor regeneration starting from deoxynucleoside monophosphates (dNMP) to deoxynucleoside diphosphates (dNDP) in the first reaction step and to dNTP in the second reaction step in the same bioreactor. The four genes encoding these deoxynucleoside monophosphate kinases were cloned into the recombinant E. coli and expressed using the recombinant E. coli strains. The reaction mechanisms and kinetics of the four kinase enzymes are studied and reported. The total enzymatic syntheses of the four dNTP products were carried out in four separate operations under the high substrate concentrations which emulate the practical application. The optimal process conditions were carefully investigated and complete conversion of dNMP to dNTP at high substrate concentration have been achieved. The purity and quality of dNTP products obtained from this work were analyzed and found to be at least equivalent or better than the commercially available dNTP products. The PCR application of dNTP products obtained from this work were also evaluated for isolating and amplifying genes of different sizes from different organisms. The PCR performance test also showed an equivalent quality as compared to the commercially available dNTP. The bioprocess technology developed and reported here for production of dNTP will provide economically competitive and environmentally friendly viable technology for the industry and research community as compared to the chemical technology currently in use.
聚合酶链反应(PCR)以及其他用于DNA合成的PCR应用需要脱氧核苷三磷酸(dNTP)作为必需的前体和底物。目前,dNTP是通过化学方法商业化生产的,该方法对环境有害且成本高昂,因为其在合成反应和纯化过程中的产率都很低。在本研究中,提出了一种用于所有dNTP组分全集成生物合成的酶技术。这里开发和报道的生物工艺技术涉及两个连续的酶促磷酸化反应,并伴随着从脱氧核苷单磷酸(dNMP)开始的辅因子再生,在第一个反应步骤中生成脱氧核苷二磷酸(dNDP),在第二个反应步骤中在同一生物反应器中生成dNTP。编码这些脱氧核苷单磷酸激酶的四个基因被克隆到重组大肠杆菌中,并使用重组大肠杆菌菌株进行表达。研究并报道了这四种激酶的反应机制和动力学。在模拟实际应用的高底物浓度下,在四个单独的操作中进行了四种dNTP产物的全酶促合成。仔细研究了最佳工艺条件,并在高底物浓度下实现了dNMP到dNTP的完全转化。分析了从这项工作中获得的dNTP产物的纯度和质量,发现其至少与市售dNTP产物相当或更好。还评估了从这项工作中获得的dNTP产物在PCR中的应用,用于从不同生物体中分离和扩增不同大小的基因。PCR性能测试也显示出与市售dNTP相当的质量。与目前使用的化学技术相比,这里开发和报道的用于生产dNTP的生物工艺技术将为工业界和研究界提供经济上有竞争力且环境友好的可行技术。