A New Enzyme for Biodiesel Production and Food Applications: Lipase of <i>Bacillus megaterium</i> F25 Isolated From an Aquatic Insect <i>Rhantus suturalis</i>
Karaman, Fatima, Incekara, Umit, Arslan, Nazli Pinar, Albayrak, Seyda, Ortucu, Serkan, Taskin, Mesut
This study aimed to isolate, purify, and characterize a lipase from the gut symbiont Bacillus megaterium F25 (GenBank accession: MF597792) of the aquatic insect Rhantus suturalis, with a focus on its potential applications in biodiesel and food industries. Under optimized culture conditions, B. megaterium F25 could produce 583 U/L of lipase in shaking flask culture. The purified lipase (PL) exhibited a specific activity with 113.89 U/mg, and its molecular weight was determined as 34 kDa. The activity of PL was enhanced by methanol, ethanol, Tween-80, Triton X-100, Ca2+, and Mg2+, while beta-mercaptoethanol, EDTA, SDS, Fe2+, Mn2+, and Cu2+ were inhibitory. PL showed optimal activity and stability at neutral and slightly acidic pHs, as well as in a temperature range of 20 degrees C-30 degrees C. PL displayed strong hydrolytic activity toward plant oils and animal fats, indicating its potency for both the food industry and the remediation of oil-contaminated environments. When tested as a catalyst, PL provided biodiesel production with a transesterification yield of 86.8% under optimized conditions (36 h reaction time, 4 mL enzyme solution, 30 degrees C, pH 7.0, and waste cooking oil:methanol ratio of 10 mL/40 mL). This is the first report on the lipase-producing potential of gut microbial symbionts of aquatic insects. Furthermore, B. megaterium lipase was tested for the first time as a biocatalyst for biodiesel production.
- Journal
- GLOBAL CHANGE BIOLOGY BIOENERGY
- Year
- 2024
- Volume
- 16
- Issue
- 12
- ISSN
- 1757-1693
- eISSN
- 1757-1707
- DOI
- 10.1111/gcbb.70009
- WoS UID
- WOS:001368674200001