Ahmad S.A.Shamaan N.A.Syed M.A.Dahalan F.A.Abdul Khalil K.Ab Rahman N.A.Shukor M.Y.2024-05-282024-05-2820171391458810.4038/jnsfsr.v45i3.81892-s2.0-85030232693https://www.scopus.com/inward/record.uri?eid=2-s2.0-85030232693&doi=10.4038%2fjnsfsr.v45i3.8189&partnerID=40&md5=13279de820c7d96b37cb0baa8b913a94https://oarep.usim.edu.my/handle/123456789/9038The purpose of this study was to investigate the ability of Acinetobacter sp. strain AQ5NOL 1 immobilised in gellan gum beads to degrade phenol in the presence of heavy metals. Seven different heavy metals, namely, As5+, Cu2+, Cd2+, Ni2+, Cr6+, Pb2+, and Hg2+ at 1 ppm were tested. Results of the study showed that degradation of phenol by free cells was inhibited by Hg2+, Cu2+ and Cr6+ after 48 hours of incubation by 97.91 %, 77.58 % and 75.26 %, respectively. Only Hg2+ and Cr6+ inhibited phenol degradation by immobilised Acinetobacter cells in 18 hours by 67.55 % and 53.19 %. Phenol degradation by immobilised cells was affected when Cr6+ and Hg2+ concentrations exceeded 0.5 and 0.1 ppm, respectively. However, inhibitory effects of heavy metals can be overcome by prolonging the incubation time for immobilised Acinetobacter sp. strain AQ5NOL 1 from 18 hours to 24 and 30 hours for Cr6+ (46.80%) and Hg2+ (21.40%), respectively. � 2017, National Science Foundation. All rights reserved.en-USAcinetobacter sp.BiodegradationHeavy metalsImmobilised cellsPhenol degradation by Acinetobacter sp. in the presence of heavy metalsJ. Natl. Sci. Found. Sri LankaArticle247253453