Velázquez-Sánchez Claudia, Espín Guadalupe, Peña Carlos, Segura Daniel
Departamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Mexico.
Departamento Ingeniería Celular y Biocatálisis, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Mexico.
Front Bioeng Biotechnol. 2020 Apr 30;8:386. doi: 10.3389/fbioe.2020.00386. eCollection 2020.
Poly-(3-hydroxyalkanoates) (PHAs) are bacterial carbon and energy storage compounds. These polymers are synthesized under conditions of nutritional imbalance, where a nutrient is growth-limiting while there is still enough carbon source in the medium. On the other side, the accumulated polymer is mobilized under conditions of nutrient accessibility or by limitation of the carbon source. Thus, it is well known that the accumulation of PHAs is affected by the availability of nutritional resources and this knowledge has been used to establish culture conditions favoring high productivities. In addition to this effect of the metabolic status on PHAs accumulation, several genetic regulatory networks have been shown to drive PHAs metabolism, so the expression of the PHAs genes is under the influence of global or specific regulators. These regulators are thought to coordinate PHAs synthesis and mobilization with the rest of bacterial physiology. While the metabolic and biochemical knowledge related to the biosynthesis of these polymers has led to the development of processes in bioreactors for high-level production and also to the establishment of strategies for metabolic engineering for the synthesis of modified biopolymers, the use of knowledge related to the regulatory circuits controlling PHAs metabolism for strain improvement is scarce. A better understanding of the genetic control systems involved could serve as the foundation for new strategies for strain modification in order to increase PHAs production or to adjust the chemical structure of these biopolymers. In this review, the regulatory systems involved in the control of PHAs metabolism are examined, with emphasis on those acting at the level of expression of the enzymes involved and their potential modification for strain improvement, both for higher titers, or manipulation of polymer properties. The case of the PHAs producer is taken as an example of the complexity and variety of systems controlling the accumulation of these interesting polymers in response to diverse situations, many of which could be engineered to improve PHAs production.
聚(3-羟基链烷酸酯)(PHA)是细菌的碳和能量储存化合物。这些聚合物在营养失衡的条件下合成,即一种营养物质限制生长,而培养基中仍有足够的碳源。另一方面,积累的聚合物在营养物质可利用的条件下或通过碳源限制被动员。因此,众所周知,PHA的积累受营养资源可用性的影响,并且这一知识已被用于建立有利于高生产率的培养条件。除了代谢状态对PHA积累的这种影响外,几个遗传调控网络已被证明驱动PHA代谢,因此PHA基因的表达受到全局或特定调节因子的影响。这些调节因子被认为将PHA的合成和动员与细菌生理学的其他方面协调起来。虽然与这些聚合物生物合成相关的代谢和生化知识已导致在生物反应器中开发高水平生产工艺,并建立了用于合成改性生物聚合物的代谢工程策略,但利用与控制PHA代谢的调控回路相关的知识进行菌株改良的情况却很少。更好地理解所涉及的遗传控制系统可以作为菌株改良新策略的基础,以提高PHA产量或调整这些生物聚合物的化学结构。在这篇综述中,研究了控制PHA代谢的调控系统,重点是那些在参与酶的表达水平起作用的系统及其对菌株改良的潜在修饰,无论是提高滴度还是操纵聚合物性质。以PHA生产者的情况为例,说明控制这些有趣聚合物积累以应对各种情况的系统的复杂性和多样性,其中许多情况可以进行工程改造以提高PHA产量。