The synthesis of bioplastic from marine microbes has a great attendance in the realm of biotechnological applications for sustainable eco-management. This study aims to isolate novel strains of poly-β-hydroxybutyrate (PHB)-producing bacteria from the mangrove rhizosphere, Red Sea, Saudi Arabia, and to characterize the extracted polymer. The efficient marine bacterial isolates were identified by the phylogenetic analysis of the 16S rRNA genes as Tamlana crocina, Bacillus aquimaris, Erythrobacter aquimaris, and Halomonas halophila. The optimization of PHB accumulation by E. aquimaris was achieved at 120 h, pH 8.0, 35 °C, and 2% NaCl, using glucose and peptone as the best carbon and nitrogen sources at a C:N ratio of 9.2:1. The characterization of the extracted biopolymer by Fourier-transform infrared spectroscopy (FTIR), Nuclear magnetic resonance (NMR), and Gas chromatography-mass spectrometry (GC-MS) proves the presence of hydroxyl, methyl, methylene, methine, and ester carbonyl groups, as well as derivative products of butanoic acid, that confirmed the structure of the polymer as PHB. This is the first report on E. aquimaris as a PHB producer, which promoted the hypothesis that marine rhizospheric bacteria were a new area of research for the production of biopolymers of commercial value.
Biobased degradable plastics have received significant attention owing to their potential application as a green alternative to synthetic plastics. A dye-based procedure was used to screen poly-3hydroxybutyrate (PHB)-producing marine bacteria isolated from the Red Sea, Saudi Arabia. Among the 56 bacterial isolates, Pseudodonghicola xiamenensis, identified using 16S rRNA gene analyses, accumulated the highest amount of PHB. The highest PHB production by P. xiamenensis was achieved after 96 h of incubation at pH 7.5 and 35 °C in the presence of 4% NaCl, and peptone was the preferred nitrogen source. The use of date syrup at 4% (w/v) resulted in a PHB concentration of 15.54 g/L and a PHB yield of 38.85% of the date syrup, with a productivity rate of 0.162 g/L/h, which could substantially improve the production cost. Structural assessment of the bioplastic by Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy revealed the presence of methyl, hydroxyl, methine, methylene, and ester carbonyl groups in the extracted polymer. The derivative products of butanoic acid estimated by gas chromatography-mass spectrometry [butanoic acid, 2-amino-4-(methylseleno), hexanoic acid, 4-methyl-, methyl ester, and hexanedioic acid, monomethyl ester] confirmed the structure of PHB. The present results are the first report on the production of a bioplastic by P. xiamenensis, suggesting that Red Sea habitats are a potential biological reservoir for novel bioplastic-producing bacteria. Petroleum-based plastic has been rapidly produced in recent decades, and its biodegradation resistance has led to a serious environmental issue for the management of solid wastes 1. The global demand for bioplastic as a substitute for synthetic plastics has increased due to its nontoxicity, renewability, biocompatibility, and biodegradability 2. Degradable biobased plastics can be produced from different renewable raw materials (polysaccharides and proteins), plants (starch-based plastics and cellulose-based plastics), and microbial bioplastics (polylactic acid and polyhydroxyalkanoates (PHAs)) 3. PHAs are the most promising type of bioplastic; they are nontoxic, biodegradable and biocompatible and have properties similar to those of conventional plastics 4. PHAs are biopolymers with diverse structures; as a defense mechanism for surviving stress conditions with nutrient imbalance, PHAs accumulate inside bacterial cells as stored energy 5. The considerable variations in functional groups from methyl to tridecyl, unsaturated bonds, and chain length make PHAs appropriate biopolymers for many different applications 6. The most common form of PHAs is poly-3-hydroxybutyrate (PHB), which accumulates in many microbes by binding β-hydroxybutyrate monomers with ester bonds 7. The universal manufacturing capacity of
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