Ahmad, SASAAhmadShamaan, NANAShamaanSyed, MAMASyedDahalan, FAFADahalanKhalil, KAKAKhalilAb Rahman, NANAAb RahmanShukor, MYMYShukor2024-05-292024-05-2920172362-01611391-458810.4038/jnsfsr.v45i3.8189WOS:000411831800006https://oarep.usim.edu.my/handle/123456789/10913The 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. Sewn different heavy metals, namely, As5+, Cu2+ Cd2+, Ni2+, Cr6+, Ph2+, and He at 1 ppm were tested. Results of the study showed that degradation of phenol by free cells was inhibited by Hg2+, Cu6+ 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 Cr 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.en-USAcinetobacter sp.biodegradationheavy metalsimmobilised cellsPhenol degradation by Acinetobacter sp in the presence of heavy metalsJ. Natl. Sci. Found. Sri LankaArticle247253453