Hendy Mahmoud H, Shehabeldine Amr M, Hashem Amr H, El-Sayed Ahmed F, El-Sheikh Hussein H
Botany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, 11884, Egypt.
Microbial Genetics Department, Biotechnology Research Institute, National Research Centre, Giza, Egypt.
BMC Microbiol. 2025 May 19;25(1):304. doi: 10.1186/s12866-025-04007-2.
The production of bioplastics from marine microorganisms is significantly relevant in the field of biotechnological applications for sustainable ecological management. Nevertheless, the expense associated with PHB production is substantial and regarded as the primary obstacle to its industrialization. In this study, orange peel waste served as a carbon source to enhance PHB production efficiency. Among the 15 strains evaluated, MH 96 was selected for PHB production due to its high salt tolerance and efficient utilization of orange peel as a substrate. The highest producing PHB strain MH96 was genetically identified using 16S rRNA sequencing as Halomonas meridiana and submitted in the GenBank under accession numbers PP826284. The optimal fermentation conditions were evaluated through single-factor optimization. Upon completion of the response surface optimization, the Plackett-Burman and Box-Behnken design experiments were conducted utilizing the outcomes of the single-factor optimization. The final parameters were the inoculum size of 1.74, (NH)HPO concentration of 1.0 and pH 6.37, and PHB yield of 5.94 g/L. The characterization of the extracted biopolymer by NMR, FTIR, XRD, and thermal properties was used to examine the properties of the extracted PHB, and gas chromatography-mass spectrometry (GC-MS) proves the presence of 2-butenoic acid, 1-methyl ethyl ester, tetradecane, hexadecanoic acid, methyl ester, and docosanoic acid, 8,9,13-trihydroxy-. Methyl ester, which confirmed the structure of the polymer as PHB.
利用海洋微生物生产生物塑料在可持续生态管理的生物技术应用领域具有重大意义。然而,与聚羟基丁酸酯(PHB)生产相关的成本很高,被视为其工业化的主要障碍。在本研究中,橙皮废料被用作碳源以提高PHB的生产效率。在评估的15株菌株中,MH 96因其高耐盐性和对橙皮作为底物的高效利用而被选用于PHB生产。利用16S rRNA测序对最高产PHB的菌株MH96进行基因鉴定,确定其为嗜盐嗜碱菌(Halomonas meridiana),并以登录号PP826284提交至GenBank。通过单因素优化评估最佳发酵条件。在响应面优化完成后,利用单因素优化的结果进行了Plackett-Burman和Box-Behnken设计实验。最终参数为接种量1.74、(NH₄)₂HPO₄浓度1.0和pH 6.37,PHB产量为5.94 g/L。通过核磁共振(NMR)、傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)和热性能对提取的生物聚合物进行表征,以研究提取的PHB的性能,气相色谱-质谱联用(GC-MS)证明存在2-丁烯酸、1-甲基乙酯、十四烷、十六烷酸甲酯和8,9,13-三羟基-二十二烷酸甲酯,这证实了该聚合物的结构为PHB。