BibTex Citation Data :
@article{Reaktor66353, author = {Chintya Lumbantoruan and Erni Misran and Zuhrina Masyithah}, title = {Provision and Identification of Local Microorganisms Based on Lake Toba Water and Its Utilization on Plastic Biodegradation}, journal = {Reaktor}, volume = {24}, number = {2}, year = {2024}, keywords = {}, abstract = { Local Microorganisms (LMO) are fermentation solutions made from agricultural, plantation and household organic waste. LMO is made by mixing three main sources of ingredients, namely a glucose source, a complex carbohydrate source, and a microorganism source which are next fermented anaerobically. The LMO solution made can be used to reduce plastic pollution through biodegradation. This research aims to analyse the variation of the volume of Lake Toba water as a source of microorganisms in making LMO which is used to degrade plastic and to identify plastic degrading local microorganisms. The research methodology consisted of making standard curves and growth curves, making LMO, testing the biodegradation of Low-Density Polyethylene (LDPE) plastic, isolating microorganisms, performing biochemical test, testing the clear zone for plastic degrading microorganisms, and identifying microorganisms. LMO was made by mixing raw materials according to the ratio of microorganism volume to substrate namely 20:80 (% v/v); 30:70 (% v/v); and 40:60 (% v/v) which were fermented for 99 hours at temperature of 37 C. The results show that there is a change in LMO pH before and after fermentation namely from 4.75; 4.9; and 4.94. to 3.46; 3.45; and 3.48. The decrease in pH occurs due to the activity of microorganisms that produced organic acids. The three variations of LMO produce degradation percentage of LDPE plastic, namely 2.353% w/w; 3.012% w/w; and 4.023% w/w. The variation ratio of 40:60 (% v/v) shows the largest percentage of LDPE degradation, which was then isolated, and 5 isolates were obtained. The five isolates were also screened to validate their potential in degrading LDPE and 2 isolates were found which produced clear zones which were identified by gram staining as Staphylococcus aureus and Streptococcus sp . }, issn = {2407-5973}, pages = {41--51} doi = {10.14710/reaktor.24.2.%p}, url = {https://ejournal.undip.ac.id/index.php/reaktor/article/view/66353} }
Refworks Citation Data :
Local Microorganisms (LMO) are fermentation solutions made from agricultural, plantation and household organicwaste. LMO is made by mixing three main sources of ingredients, namely a glucose source, a complex carbohydratesource, and a microorganism source which are next fermented anaerobically. The LMO solution made can be usedto reduce plastic pollution through biodegradation. This research aims to analyse the variation of the volume of LakeToba water as a source of microorganisms in making LMO which is used to degrade plastic and to identify plasticdegrading local microorganisms. The research methodology consisted of making standard curves and growth curves,making LMO, testing the biodegradation of Low-Density Polyethylene (LDPE) plastic, isolating microorganisms,performing biochemical test, testing the clear zone for plastic degrading microorganisms, and identifyingmicroorganisms. LMO was made by mixing raw materials according to the ratio of microorganism volume tosubstrate namely 20:80 (% v/v); 30:70 (% v/v); and 40:60 (% v/v) which were fermented for 99 hours at temperatureof 37 C. The results show that there is a change in LMO pH before and after fermentation namely from 4.75; 4.9;and 4.94. to 3.46; 3.45; and 3.48. The decrease in pH occurs due to the activity of microorganisms that producedorganic acids. The three variations of LMO produce degradation percentage of LDPE plastic, namely 2.353% w/w;3.012% w/w; and 4.023% w/w. The variation ratio of 40:60 (% v/v) shows the largest percentage of LDPEdegradation, which was then isolated, and 5 isolates were obtained. The five isolates were also screened to validatetheir potential in degrading LDPE and 2 isolates were found which produced clear zones which were identified bygram staining as Staphylococcus aureus and Streptococcus sp.
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Last update: 2024-12-19 23:06:45
JURNAL REAKTOR (p-ISSN: 0852-0798; e-ISSN: 2407-5973)
Published by Departement of Chemical Engineering, Diponegoro University