Recovery of polyhydroxyalkanoate from the newly identified strain Enterobacter sp. MPLSI-2 isolated from a plastic waste landfill

Synthetic plastic waste poses a severe environmental threat due to its persistence and accumulation. As a result, producing biodegradable alternatives like polyhydroxyalkanoates (PHAs) is essential to replace conventional plastics and mitigate this pollution crisis. We isolated a novel Enterobacter sp. (MPLSI-2, PV029923) from a plastic waste landfill, a stress-rich and underexplored niche for identifying PHA producers. This study reports the first bioproduction of a novel seven-monomer medium- and long-chain copolymer, P(3HHxD-co-3HHxDe-co-3HOD-co-3HODe-co-3HTeD-co-3HTrD-co-3HHeD), by Enterobacter sp. MPLSI-2. Notably, the complex PHA was synthesized directly from glucose as the sole carbon source. The isolate identified via 16S rRNA sequencing as Enterobacter sp. MPLSI-2 (GenBank accession number: PV029923). Phylogenetic analysis and nucleotide homology confirmed the strain shares 99.44% sequence similarity with Enterobacter bugandensis EB-247 (FYBI01000003). The isolate is a Gram-negative, non-spore-forming rod, positive for citrate utilization and for amylase and protease production. Initial screening using Sudan Black B, Nile Blue A, and PHA-selective media revealed intracellular PHA granules, which were confirmed by microscopic observation. Using a One-Factor-At-A-Time (OFAT) design, culture conditions (temperature, pH) and carbon sources were optimized. Maximum PHA accumulation occurred at 37 °C and pH 7 using glucose (52.1 ± 1.87% DCW), followed by molasses (37.9 ± 0.66% DCW). The achieved productivity highlights the viability of molasses as an alternative substrate. Among recovery methods tested, SDS pretreatment followed by solvent extraction gave the highest extraction yield (74.7 ± 3.72%). While FTIR analysis suggested the characteristic ester carbonyl and alkyl bands indicative of PHAs, complementary GC–MS profiling definitively identified the polymer as a complex seven-monomer copolymer consisting of P(3HHxD-co-3HHxDe-co-3HOD-co-3HODe-co-3HTeD-co-3HTrD-co-3HHeD). These results indicate that Enterobacter sp. MPLSI-2 can produce substantial PHA from both pure and agro-industrial substrates and that optimized recovery improves overall yield.

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Publication Details

Journal
Discover Applied Sciences
Published
2026-08-26
DOI
https://doi.org/10.1007/s42452-026-09400-8
Primary Topic
biodegradable polymer synthesis and properties
Type
article
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article

Recovery of polyhydroxyalkanoate from the newly identified strain Enterobacter sp. MPLSI-2 isolated from a plastic waste landfill

Leta Guta Inki, Seid Mohammed Ebu, Osman Ahmed Zelekew, Berhanu Abegaz Mulat
Discover Applied Sciences
biodegradable polymer synthesis and properties
article

Recovery of polyhydroxyalkanoate from the newly identified strain Enterobacter sp. MPLSI-2 isolated from a plastic waste landfill

Leta Guta Inki, Seid Mohammed Ebu, Osman Ahmed Zelekew, Berhanu Abegaz Mulat
article en

Abstract

Synthetic plastic waste poses a severe environmental threat due to its persistence and accumulation. As a result, producing biodegradable alternatives like polyhydroxyalkanoates (PHAs) is essential to replace conventional plastics and mitigate this pollution crisis. We isolated a novel Enterobacter sp. (MPLSI-2, PV029923) from a plastic waste landfill, a stress-rich and underexplored niche for identifying PHA producers. This study reports the first bioproduction of a novel seven-monomer medium- and long-chain copolymer, P(3HHxD-co-3HHxDe-co-3HOD-co-3HODe-co-3HTeD-co-3HTrD-co-3HHeD), by Enterobacter sp. MPLSI-2. Notably, the complex PHA was synthesized directly from glucose as the sole carbon source. The isolate identified via 16S rRNA sequencing as Enterobacter sp. MPLSI-2 (GenBank accession number: PV029923). Phylogenetic analysis and nucleotide homology confirmed the strain shares 99.44% sequence similarity with Enterobacter bugandensis EB-247 (FYBI01000003). The isolate is a Gram-negative, non-spore-forming rod, positive for citrate utilization and for amylase and protease production. Initial screening using Sudan Black B, Nile Blue A, and PHA-selective media revealed intracellular PHA granules, which were confirmed by microscopic observation. Using a One-Factor-At-A-Time (OFAT) design, culture conditions (temperature, pH) and carbon sources were optimized. Maximum PHA accumulation occurred at 37 °C and pH 7 using glucose (52.1 ± 1.87% DCW), followed by molasses (37.9 ± 0.66% DCW). The achieved productivity highlights the viability of molasses as an alternative substrate. Among recovery methods tested, SDS pretreatment followed by solvent extraction gave the highest extraction yield (74.7 ± 3.72%). While FTIR analysis suggested the characteristic ester carbonyl and alkyl bands indicative of PHAs, complementary GC–MS profiling definitively identified the polymer as a complex seven-monomer copolymer consisting of P(3HHxD-co-3HHxDe-co-3HOD-co-3HODe-co-3HTeD-co-3HTrD-co-3HHeD). These results indicate that Enterobacter sp. MPLSI-2 can produce substantial PHA from both pure and agro-industrial substrates and that optimized recovery improves overall yield.

Discover Applied Sciences
Adama Science and Technology University (ET)
Responsible consumption and production
Openalex Percentile: Top 19%
biodegradable polymer synthesis and properties
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