Thomas Tatiana, Sudesh Kumar, Bazire Alexis, Elain Anne, Tan Hua Tiang, Lim Hui, Bruzaud Stéphane
Institut de Recherche Dupuy de Lôme (IRDL), Université de Bretagne Sud (UBS), EA 3884 Lorient, France.
Institut de Recherche Dupuy de Lôme (IRDL), Université de Bretagne Sud (UBS), 56300 Pontivy, France.
Bioengineering (Basel). 2020 Mar 20;7(1):29. doi: 10.3390/bioengineering7010029.
Among the different tools which can be studied and managed to tailor-make polyhydroxyalkanoates (PHAs) and enhance their production, bacterial strain and carbon substrates are essential. The assimilation of carbon sources is dependent on bacterial strain's metabolism and consequently cannot be dissociated. Both must wisely be studied and well selected to ensure the highest production yield of PHAs. sp. SF2003 is a marine bacterium already identified as a PHA-producing strain and especially of poly-3-hydroxybutyrate (P-3HB) and poly-3-hydroxybutyrate--3-hydroxyvalerate (P-3HB--3HV). Previous studies have identified different genes potentially involved in PHA production by sp. SF2003, including two genes with atypical characteristics, and . At the same time, an interesting adaptability of the strain in front of various growth conditions was highlighted, making it a good candidate for biotechnological applications. To continue the characterization of sp. SF2003, the screening of carbon substrates exploitable for PHA production was performed as well as production tests. Additionally, the functionality of both PHA synthases PhaC1 and PhaC2 was investigated, with an study and the production of transformant strains, in order to confirm and to understand the role of each one on PHA production. The results of this study confirm the adaptability of the strain and its ability to exploit various carbon substrates, in pure or mixed form, for PHA production. Individual expression of PhaC1 and PhaC2 synthases in a non-PHA-producing strain, H16 PHB¯4 (DSM 541), allows obtaining PHA production, demonstrating at the same time, functionality and differences between both PHA synthases. All the results of this study confirm the biotechnological interest in sp. SF2003.
在可用于研究和调控以定制聚羟基脂肪酸酯(PHA)并提高其产量的不同工具中,菌株和碳源至关重要。碳源的同化依赖于菌株的代谢,因此二者不可分割。必须对它们进行明智的研究和精心选择,以确保PHA的最高产量。sp. SF2003是一种已被鉴定为PHA生产菌株的海洋细菌,尤其能产生聚-3-羟基丁酸酯(P-3HB)和聚-3-羟基丁酸酯-3-羟基戊酸酯(P-3HB-3HV)。先前的研究已确定sp. SF2003中可能参与PHA生产的不同基因,包括两个具有非典型特征的基因, 和 。同时,该菌株在各种生长条件下展现出有趣的适应性,使其成为生物技术应用的良好候选对象。为了继续对sp. SF2003进行表征,开展了用于PHA生产的可利用碳源的筛选以及生产测试。此外,还通过 研究和转化菌株的生产,对两种PHA合酶PhaC1和PhaC2的功能进行了研究,以确认并了解它们各自在PHA生产中的作用。本研究结果证实了该菌株的适应性及其利用各种纯形式或混合形式的碳源进行PHA生产的能力。在非PHA生产菌株H16 PHB¯4(DSM 541)中单独表达PhaC1和PhaC2合酶可实现PHA生产,同时证明了两种PHA合酶的功能及差异。本研究的所有结果证实了sp. SF2003在生物技术方面的价值。