School of Biotechnology, State Key Laboratory of Bioreactor Engineering, R&D Center of Separation and Extraction Technology in Fermentation Industry, East China University of Science and Technology, Shanghai, 200237, China.
Shanghai Collaborative Innovation Center for Biomanufacturing Technology (SCICBT), Shanghai, 200237, China.
Appl Biochem Biotechnol. 2019 Oct;189(2):411-423. doi: 10.1007/s12010-019-03004-2. Epub 2019 Apr 30.
Poly-γ-glutamic acid (γ-PGA) is a novel biodegradable polyamide material. Microbial fermentation is the only way to produce γ-PGA, but the molecular weight of γ-PGA varied depending on different strains and culture conditions used. The molecular weight of γ-PGA is a main factor affecting the utilization of γ-PGA. It is urgent to find an efficient way to prepare γ-PGA with specific molecular weight, especially low molecular weight. Bacillus subtilis ECUST is a glutamate-dependent strain that produces γ-PGA. In this study, a recombinant B. subtilis harboring the γ-PGA synthase gene cluster pgsBCAE of our preciously identified γ-PGA-producing B. subtilis ECUST was constructed. Assay of γ-PGA contents and properties showed that recombinant B. subtilis 1A751-pBNS2-pgsBCAE obtained the ability to synthesize γ-PGA with low molecular weight (about 10 kDa). The excessive addition of glutamate inhibited the γ-PGA synthesis, while the addition of Zn could promote the synthesis of γ-PGA by increasing the transcription of pgsB but had no effect on the molecular weight of synthesized γ-PGA. Under optimized conditions, γ-PGA produced by recombinant B. subtilis 1A751-pBNS2-pgsBCAE increased from initial 0.54 g/L to 3.9 g/L, and the glutamate conversion rate reached 78%. Recombinant B. subtilis 1A751-pBNS2-pgsBCAE has the potential for efficient preparation of low molecular weight γ-PGA.
聚-γ-谷氨酸(γ-PGA)是一种新型可生物降解的聚酰胺材料。微生物发酵是生产 γ-PGA 的唯一途径,但 γ-PGA 的分子量因使用的不同菌株和培养条件而异。γ-PGA 的分子量是影响其利用的主要因素。迫切需要找到一种有效的方法来制备具有特定分子量的 γ-PGA,特别是低分子量的 γ-PGA。枯草芽孢杆菌 ECUST 是一种依赖谷氨酸的菌株,能够产生 γ-PGA。在本研究中,构建了一株携带我们先前鉴定的产 γ-PGA 枯草芽孢杆菌 ECUST 的 γ-PGA 合酶基因簇 pgsBCAE 的重组枯草芽孢杆菌。γ-PGA 含量和性质的测定表明,获得的重组枯草芽孢杆菌 1A751-pBNS2-pgsBCAE 具有合成低分子量(约 10 kDa)γ-PGA 的能力。谷氨酸的过量添加抑制了 γ-PGA 的合成,而 Zn 的添加可以通过增加 pgsB 的转录来促进 γ-PGA 的合成,但对合成的 γ-PGA 的分子量没有影响。在优化条件下,重组枯草芽孢杆菌 1A751-pBNS2-pgsBCAE 生产的 γ-PGA 从初始的 0.54 g/L 增加到 3.9 g/L,谷氨酸转化率达到 78%。重组枯草芽孢杆菌 1A751-pBNS2-pgsBCAE 具有高效制备低分子量 γ-PGA 的潜力。