›› 2015, Vol. 17 ›› Issue (2): 72-80.DOI: 10.13304/j.nykjdb.2015.088

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Heterologous Expression of 6-phosphofructo Kinase Gene pfkA from Escherichia coli in Pseudomonas stutzeri and Phenotype Analysis of Recombinant Strain

HU Tao1,2, MA Yao2, ZHAN Yu-hua2, LU Wei2, HUANG He1, LIN Min2, YAN Yong-liang2*   

  1. (1.College of Food Science and Light Industry, Nanjing University of Technology, Nanjing 211816|2.Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China)
  • Received:2015-02-10 Revised:2015-03-09 Online:2015-04-15 Published:2015-04-15

6-磷酸果糖激酶基因pfkA在施氏假单胞菌中的异源表达及其表型分析

胡涛1,2,马尧2,战嵛华2,陆伟2,黄和1,林敏2,燕永亮2*   

  1. (1.南京工业大学食品与轻工学院, 南京 211816|2.中国农业科学院生物技术研究所, 北京 100081)
  • 通讯作者: 燕永亮,副研究员,博士,硕士生导师,主要从事微生物分子生物学及基因工程研究。E-mail:yanyongliang@caas.cn
  • 作者简介:胡涛|硕士研究生|研究方向固氮微生物与基因工程。E-mail:htaaaa081@126.com。
  • 基金资助:

    国家自然科学基金项目(31470205;31400076);国家863计划项目(2012AA02A703);中央级科研院所基本业务费专项;广东省引进创新创业团队计划项目(2013S033)资助。

Abstract:

Sugar metabolism is the process operated by nearly all organisms for the supplement of nutrition and energy. As one of the most widely used monosaccharides in nature, glucose is an ideal carbon source for microorganisms. Pseudomonas stutzeri A1501 has the canonica microbial metabolic pathways. However, it has a very low rate for glucose utilization. Genome analysis of P. stutzeri A1501 suggested that A1501 could not use glucose by the Embden-Meyerhof-Parnas (EMP) pathway, because it lacked the key glycolytic enzyme 6-phosphofructokinase encoded by pfkA. An Escherichia coli pfkA gene was cloned and transferred to P. stutzeri A1501 to accomplish the reconstruction in vivo of the complete set of enzymes for enabling a functional EMP pathway in A1501. The expression of pfkA in P. stutzeri A1501 failed to glucose utilization by the EMP pathway, suggesting that there were other systems that might affect the glucose utilization except for the pfkA gene. It was also observed that the recombinant A1501-pfkA strain became more sensitive to hydrogen peroxide, compared to the wild type. We further hypothesized that the major reason for pfkA confers decreased oxidative tolerance to P. stutzeri A1501 was due to the influence of its NADPH formation.

Key words: Pseudomonas stutzeri A1501, glucose, EMP pathway, 6-phosphofructokinase

摘要:

糖代谢在生命活动中具有重要意义,它保证了生物体生命活动所需的物质和能量的供应。葡萄糖作为自然界中普遍存在的最简单的单糖,是生物体的理想碳源。施氏假单胞菌(Pseudomonas stutzeri)A1501具有广泛的、典型的微生物代谢途径,但是该菌利用葡萄糖的效率很低。基因组分析表明A1501菌缺少糖酵解(EMP)途径中编码6-磷酸果糖激酶的基因pfkA,初步认为这可能是A1501菌不能高效利用葡萄糖的原因。利用穿梭质粒pLAFR3将大肠杆菌的pfkA基因导入到施氏假单胞菌中,通过pfkA基因的异源表达重建A1501菌的EMP途径。测定了重组菌株的糖类代谢能力,结果表明pfkA基因的导入并没有赋予重组施氏假单胞菌更强的葡萄糖及其他糖类的利用能力,说明A1501菌葡萄糖利用的低效率除了缺乏pfkA外,还有其他的因素。研究也发现,导入pfkA的重组施氏假单胞菌对H2O2高度敏感,推测pfkA导入重建后的EMP途径可能影响了该菌的还原力合成,导致菌体对氧化胁迫的耐受能力降低。

关键词: 施氏假单胞菌A1501;葡萄糖;糖酵解途径;6-磷酸果糖激酶

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