Complete Degradation of Hexahydro‐1,3,5‐Trinitro‐1,3,5‐Triazine (RDX) by a Co‐Culture of Gordonia sp. KTR9 and Methylobacterium sp. JS178

The presence of hexahydro‐1,3,5‐trinitro‐1,3,5‐triazine (RDX) in soil and groundwater is a major contamination issue at many military facilities around the world. Gordonia sp. KTR9 metabolizes RDX as a nitrogen source for growth producing 4‐nitro‐2,4‐diazabutanal (NDAB) as a dead‐end product. Methylobacterium sp. strain JS178 degrades NDAB as a sole source of nitrogen for growth. A mixed culture of strains KTR9 and JS178 was able to completely degrade RDX. There was no difference in rate of RDX degradation by KTR9 alone or in co‐culture with JS178. The first‐order degradation coefficients of RDX and NDAB in the co‐culture were 0.08 hr^?1 and 0.002 hr^?1, respectively. In the co‐culture that initially contained RDX plus NDAB, strain JS178 degraded the NDAB that was produced by KTR9 as shown by a decrease in the molar yield of NDAB (from RDX) from 1.0 to –0.11. Co‐cultures of strains KTR9 and JS178 could be used to promote complete degradation of RDX in soils or groundwater. ©2016 Wiley Periodicals, Inc.     

Identification of pyrene‐degradation pathways: Bench‐scale studies using Pseudomonas fluorescens 29L

This article summarizes the bench‐scale studies to identify pyrene‐degradation pathways using an environmental microbial isolate, Pseudomonas fluorescens 29L. Strain 29L was grown on 50 mg of pyrene per liter of mineral medium. At a pyrene biodegradation rate of 14.7 mg/L of medium/day, 82.38 percent of pyrene was degraded in six days. Naphthalene and phenanthrene accounted for 1.09 percent and 3.69 percent, respectively, of the carbon mass from pyrene in the late log phase. Substituted benzene compounds accounted for 26.10 percent of the carbon mass from pyrene in the late log phase. In the stationary phase, carboxylic acids accounted for 10.44 percent of the carbon mass from pyrene. Strain 29L mutants were used for enzyme assays. Pyrene is oxidized by monoxygenases and dioxygenases, and the oxidized ring is cleaved. These enzymes were induced in the presence of pyrene and their activities peaked in the late log phase. No gentisate 1,2‐dioxygenase activity was detected in Strain 29L wild type (WT), whereas mutant M15 did not show any catechol 2,3‐dioxygenase activity. This indicates the possibility of multiple branchings in the pyrene‐biodegradation pathways. In conclusion, multiple degradative pathways are operating concurrently in this strain. The study shows the versatility of Pseudomonas fluorescens Strain 29L for pyrene degradation. It also emphasizes the need to study pyrene‐degradation pathways in other microorganisms so as to enhance the bioremediation potential for the in situ treatment of pyrene‐contaminated sites. © 2008 Wiley Periodicals, Inc.     

共基质和无机盐对原油降解菌株降解原油效果的影响

从大港油田石油污染土壤中分离筛选出1株原油降解菌X3,对原油的降解率达72．6％,经鉴定X3菌株属于假单胞菌属（Psedomonas）。利用生物摇床对X3菌株降解原油的实验发现,共代谢基质α-乳糖对X3菌株降解原油有促进作用,可使原油降解率提高到80．3％;而葡萄糖和蔗糖对X3菌株降解原油有抑制作用。Fe2＋对X3菌株的降解原油也有促进作用,在α-乳糖和Fe2＋的共同作用下,X3菌株对原油的降解率可达82．3％;K＋和Mg2＋对X3菌株降解原油则有抑制作用。在FeSO4质量浓度为0．2～0．3mg／L时,X3菌株对原油的降解率最高,FeSO4质量浓度继续增加,X3菌株对原油的降解率下降。     

Effects of physicochemical factors on PAH degradation by Planomicrobium alkanoclasticum

Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants that are mutagenic, carcinogenic, and toxic to living organisms. Here, the ability and effectiveness of selected bacteria isolated from an oil‐contaminated area in biodegrading PAHs were evaluated, and the optimal conditions conducive to bacterial PAH biodegradation were determined. Of six bacterial isolates identified based on their 16S rRNA sequences, Planomicrobium alkanoclasticum could subsist on and consume nearly all hydrocarbons according to the 2,6‐dichlorophenolindophenol assay. The efficacy of this isolate at PAH biodegradation was then empirically confirmed. After 30 days of incubation, P. alkanoclasticum degraded 90.8% of the 16 PAH compounds analyzed and fully degraded eight of them. The optimum P. alkanoclasticum growth conditions were 35°C, pH 7.5, and NaNO₃ as the nitrogen source. Under these biostimulant conditions, P. alkanoclasticum degraded 91.4% of the total PAH concentration and completely decomposed seven PAHs after 15 days incubation. Hence, P. alkanoclasticum is an apt candidate for the biodegradation of PAHs and the bioremediation of sites contaminated by them.     

过氧化氢、过碳酸钠活化过硫酸钠氧化—微生物降解联用技术修复原油污染土壤

分别以H₂O₂和Na₂CO₃·1.5H₂O₂活化Na₂S₂O₄降解原油污染土壤,考察氧化后土壤的原油降解率、pH、微生物含量以及原油组分的变化,比较两种活化剂对过硫酸钠氧化—微生物降解联用技术修复原油污染土壤效果的影响。实验结果表明：两种活化剂氧化处理7 d后的最大原油降解率分别达到42.94%和44.07%;氧化后原油组分的占比情况发生变化,w（饱和烃）增加5.28~11.93个百分点,而w（芳香烃）、w（胶质）和w（沥青质）则分别降低了0.10~2.53,2.53~3.80,0.94~3.43个百分点;添加微生物菌剂进行50 d的生物降解后,两种活化剂的最大原油降解率分别达到71.00%和75.70%,比单独微生物降解时提高了5.96~12.08个百分点。     

Pseudomonas sp. (Strain 10–1B): A potential inoculum candidate for green and sustainable remediation

Soil pollution caused by polycyclic aromatic hydrocarbons (PAHs) is a consequence of various industrial processes which destabilizes the ecosystem. Bioremediation by bacteria is a cost‐effective and environmentally safe solution for reducing or eliminating pollutants in soils. In the present study, we artificially polluted agricultural soil with used automobile engine oil with a high PAH content and then isolated bacteria from the soil after 10 weeks. Pseudomonas sp. strain 10–1B was isolated from the bacterial community that endured this artificial pollution. We sequenced its genomic DNA on Illumina MiSeq sequencer and evaluated its ability to solubilize phosphate, fix atmospheric nitrogen, and produce indoleacetic acid, in vitro, to ascertain its potential for contribution to soil fertility. Its genome annotation predicted several dioxygenases, reductases, ferredoxin, and Rieske proteins important in the ring hydroxylation initiating PAH degradation. The strain was positive for the soil fertility attributes evaluated. Such combination of attributes is important for any potential bacterium partaking in sustainable bioremediation of PAH‐polluted soil.     

Factors affecting polycyclic aromatic hydrocarbon biodegradation by Aspergillus flavus

This study investigated the ability of fungi isolated from highly contaminated soil to biodegrade polycyclic aromatic hydrocarbon (PAH) compounds, as well as the effect of several parameters on the biodegradation ability of these fungi. The isolated fungi were identified using ITS rDNA sequencing and tested using 2,6‐dichlorophinolendophenol to determine their preliminary ability to degrade crude oil. The top‐performing fungi, Aspergillus flavus and Aspergillus fumigatus, were selected to test their ability to biodegrade PAH compounds as single isolates. After 15 days of incubation, A. flavus degraded 82.7% of the total PAH compounds, with the complete degradation of six compounds, whereas A. fumigatus degraded 68.9% of the total PAHs, with four aromatic compounds completely degraded. We also tested whether different temperatures, pH, and nitrogen sources influenced the growth of A. flavus and the degradation rate. The degradation process was optimal at a temperature of 30°C, pH of 5.5, and with nitrogen in the form of yeast extract. Finally, the ability of the fungal candidate, A. flavus, to degrade PAH compounds under these optimum conditions was studied. The results showed that 95.87% of the total PAHs, including 11 aromatic compounds, were completely degraded after 15 days of incubation. This suggests that A. flavus is a potential microorganism for the degradation of PAH compounds in aqueous cultures.     

超声-紫外光协同催化体系降解水中菲

以纳米TiO_2为催化剂,采用超声-紫外光协同催化体系降解水中菲,并考察了菲降解率的影响因素。实验结果表明:不同类型TiO_2对菲降解率的大小顺序为锐钛矿型TiO_2P25型TiO_2金红石型TiO_2;超声-紫外光协同催化体系对菲的降解率大于单独超声体系或紫外光催化体系,且均遵从一级反应动力学规律;在超声频率为60k Hz、声强为0.233 W/cm2、TiO_2投加量为0.06 g/L、pH为4.0、H_2O_2浓度为19.59 mmol/L的条件下降解75 min后,超声-紫外光协同催化体系对初始质量浓度为0.96 mg/L的菲的降解率可达76.78%。     

Complex co‐substrate addition increases initial petroleum degradation rates during land treatment by altering bacterial community physiology

A pilot‐scale land treatment unit (LTU) was constructed at the former Guadalupe oil production field with the purpose of investigating the effect of co‐substrate addition on the bacterial community and the resulting rate and extent of total petroleum hydrocarbon (TPH) degradation. The TPH was a weathered mid‐cut distillate (C10‐C32) excavated from the subsurface and stockpiled before treatment. A control cell (Cell 1) in the LTU was amended with nitrogen and phosphorus while the experimental cell (Cell 2) was amended with additional complex co‐substrate—corn steep liquor. During the pilot LTU operation, measurements were taken of TPH, nutrients, moisture, aerobic heterotrophic bacteria (AHB), and diesel oxidizing bacteria (DOB). The bacterial community was also assayed using community‐level physiology profiles (CLPP) and 16S rDNA terminal restriction fragment (TRF) analysis. TPH degradation in both cells was characterized by a rapid phase of degradation that lasted for the first three weeks, followed by a slower degradation phase that continued through the remainder of the project. The initial rate of TPH‐degradation in Cell 1 (?0.021 day^?1) was slower than in Cell 2 (?0.035 day^?1). During the slower phase, degradation rates in both cells were similar (?0.0026 and ?0.0024 respectively). AHB and DOB counts were similar in both cells during the fast degradation phase. A second addition of co‐substrate to Cell 2 at the beginning of the slow degradation phase resulted in an increased AHB population that lasted for the remainder of the project but did not affect TPH degradation rates. CLPP data showed that co‐substrate addition altered the functional capacity of the bacterial community during both phases of the project. However, TRF data indicated that the phylogenetic composition of the community was not different in the two cells during the fast degradation phase. The bacterial phylogenetic structure in Cell 2 differed from Cell 1 after the second application of co‐substrate, during the slow degradation phase. Thus, co‐substrate addition appeared to enhance the functional capacity of the bacterial community during the fast degradation phase when the majority of TPH was bioavailable, resulting in increased degradation rates, but did not affect rates during the slow degradation phase when the remaining TPH may not have been bioavailable. These data show that co‐substrate addition might prove most useful for applications such as land farming where TPH is regularly applied to the same soil and initial degradation rates are more important to the project goals. © 2003 Wiley Periodicals, Inc.     

Biodegradation of Polycyclic Aromatic Hydrocarbons by Exopolymers Synthesized by Moderately Halophilic Bacteria: Chemical Composition and Functional Properties

Three strains of halophilic bioemulsifier-producing bacteria; Bacillus sp. 2BSG-PDA-16, Bacillus sp. DV2-37 and Bacillus licheniformis ABRII6 were isolated from crude oil polluted water samples. Characteristics of exopolymers produced by these strains in media supplemented with various hydrocarbons instead of glucose were studied. Yield production, chemical composition, emulsifying, rheological and flocculating properties of exopolymers varied according to the strain and the carbon source. The highest amount of exopolymers synthesized by Bacillus sp. 2BSG-PDA-16, Bacillus sp. DV2-37 and B. licheniformis ABRII6 was 11, 18.5 and 12.4 g/l, respectively from media amended with glucose, while the most active emulsifiers were those obtained from media added with crude oil. Furthermore, all exopolymers produced were capable of emulsifying crude oil more efficiently than the three chemical surfactants tested as control (Tween 20, Tween 80 and Triton X-100). Respect to chemical composition, exopolymers produced on hydrocarbons always have lower content of carbohydrates and proteins than exopolymers produced in medium amended with glucose, however they showed higher amounts of uronic acids, sulfates and acetyl residues. The rheological study suggested that the exopolymers have characteristics of the pseudoplastic fluids. Efficiency of bacterial strains to remove PAH seems to agree with their potential applicability in oil bioremediation technology.     

Optimization of Poly(<Emphasis Type="SmallCaps">dl</Emphasis>-Lactic Acid) Degradation and Evaluation of Biological Re-polymerization

Poly(dl-lactic acid) or PLA is a biodegradable polymer. It has received much attention since it plays an important role in resolving the global warming problem. The protease produced by Actinomadura keratinilytica strain T16-1 was previously reported as having PLA depolymerase potential and being applicable to PLA biodegradation, which was used in this work. Therefore, this research demonstrates the important basic knowledge on the biological degradation process by the crude PLA-degrading enzyme from strain T16-1. Its re-polymerization was evaluated. The optimization of PLA degradation by statistical methods based on central composite design was determined. Approximately 6700 mg/l PLA powder was degraded by the crude enzyme under optimized conditions: an initial enzyme activity of 200 U/ml, incubated at 60 °C for 24 h released 6843 mg/l lactic acid with 82% conversion, which was similar to the commercial enzyme proteinase K (81%). The degradable products were re-polymerized repeatedly by using commercial lipase as a catalyst under a nitrogen atmosphere for 6 h. A PLA oligomer was achieved with a molecular weight of 378 Da (n = 5). This is the first report to demonstrate the high efficiency of the enzyme to degrade 100% of PLA powder and to show the biological recycling process of PLA, which is promising for the treatment and utilization of biodegradable plastic wastes in the future.     

Lysinibacillus sphaericus and Geobacillus sp Biodegradation of Petroleum Hydrocarbons and Biosurfactant Production

Petroleum oil is a major driver of worldwide economic activity, but it has also created contamination problems during the storage and refining process. Also, unconventional resources are natural resources, which require greater than industry‐standard levels of technology or investment to exploit. In the case of unconventional hydrocarbon resources, additional technology, energy, and capital have to be applied to extract the gas or oil. Bioremediation of petroleum spill is considered of great importance due to the contaminating effects on human health and the environment. For this reason, it is important to reduce total petroleum hydrocarbons (TPH) in contaminated soil. In addition, biosurfactant production is a desirable property of hydrocarbon‐degrading microorganisms. Seven strains belonging to Lysinibacillus sphaericus and Geobacillus sp were selected to evaluate their ability to biodegrade TPH in the presence of toxic metals, their potential to produce biosurfactants, and their ability to improve the biodegradation rate. The seven bacterial strains examined in this study were able to utilize crude petroleum‐oil hydrocarbons as the sole source of carbon and energy. In addition, their ability to degrade crude oil was not affected by the presence of toxic metals such as chromium and arsenic. At the same time, the strains were able to reduce toxic metals concentration through biosorption processes. Biosurfactant production was determined using the drop‐collapsed method for all strains, and they were characterized as both anionic and cationic biosurfactants. Biosurfactants showed an increase in biodegradation efficiency both in liquid minimal salt medium and landfarming treatments. The final results in field tests showed an efficiency of 93 percent reduction in crude oil concentration by the selected consortium compared to soil without consortium. The authors propose L. sphaericus and Geobacillus sp consortium as an optimum treatment for contaminated soils. In addition, production of biosurfactants could have an application in the extraction of crude oil from unconventional hydrocarbon resources. © 2014 Wiley Periodicals, Inc.     

萘降解菌的筛选及其对多环芳烃的降解

从柴油污染土壤中筛选分离出一株萘降解菌N-3,进行了菌种鉴定及萘双加氧酶基因(nah)验证,并考察了该菌对不同种类多环芳烃(PAHs)的降解能力及降解过程中脱氢酶活性的变化。实验结果表明:该菌为铜绿假单胞菌(Pseudomonas aeruginosa),含有nah基因;当分别对液体培养基中质量浓度为50 mg/L的萘、菲、蒽、芘、芴降解84 h时,菌株N-3对萘、菲、蒽、芘、芴的降解率分别为28.81%,34.83%,36.65%,27.50%,23.47%。菌株N-3的脱氢酶活性与其对不同PAHs的降解率呈一定的正相关性。该菌不仅能有效降解萘,且对其他种类PAHs也有一定降解作用。     

微生物降解重油的初步研究

丛石油污染的土壤中筛选出一株假单胞菌,考察了其对重油的降解效果。降解18d,重油的降解率达到42．8％,饱和烃、芳香烃、胶质、沥青质的降解率分别为42．95％,43．85％,44．5％,5．55％;质量浓度2．5g／L的表面活性剂Tween-80可使重油的18d降解率达到51．0％;弱碱性条件有利于重油的生物降解;生物泥浆法处理重油污染的土壤,1kg土壤中重油质量100g,降解45d,重油的降解率达到38．85％。     

A design tool for planning emulsified oil‐injection systems

Emulsified oils have been used to stimulate anaerobic bioremediation at hundreds of sites contaminated with chlorinated solvents, perchlorate, heavy metals, and nitrate. A simple spreadsheet‐based tool has been developed to assist in the design of injection‐only systems for distributing emulsified oils in barriers and area treatments. This tool allows users to quickly compare the relative costs and performance of different injection alternatives and identify a design that is best suited to site‐specific conditions. Contact efficiency is estimated using results of prior numerical model simulations and dimensionless scaling factors that relate the volume of oil and water injected to treatment‐zone dimensions. Sensitivity analysis results indicate that maximum oil retention is one of the most important factors controlling system performance and cost. © 2008 Wiley Periodicals, Inc.     

Bioremediation of petroleum‐impacted soils from investigation‐derived wastes

Optimal conditions for bioremediation of investigation‐derived wastes from petroleum‐impacted soils (PIS) were determined through biotreatability experiments. The PIS was collected as extruded cores obtained during sample drilling. These samples were processed into workable media prior to treatment in bioreactors. Soil moisture content in the bioreactors was adjusted to 30 percent, 40 percent, 50 percent (control), and 60 percent, dry‐weight basis, and nutrient levels were adjusted by applying fertilizer, yielding carbon (C) to nitrogen (N) ratios of 20:1, 10:1, and 5:1, versus a control C:N ratio of 140:1. Temperature, pH, viable bacterial plate counts, contaminant degradation rate, and microbial respiration were monitored. Concentrations of three selected branched alkanes in the aviation fuel contaminant, measured by gas chromatography, decreased for most treatments. The greatest degradation occurred with a moisture content of 40 percent and C:N ratio of 5:1. Increased contaminant degradation was consistent with increased microbial activity measured by respiration. There was poorer correlation between contaminant degradation and viable plate counts, which suggests that respirometry is a better measure of activity of the microbial population responsible for contaminant degradation. General plate counts, which enumerate only a fraction of the total population, may not be a reliable quantitative indicator of the actual microorganism population that is responsible for degradation. © 2003 Wiley Periodicals, Inc.     

Planning‐level source decay models to evaluate impact of source depletion on remediation time frame

A recent United States Environmental Protection Agency (US EPA) Expert Panel on Dense Nonaqueous Phase Liquid (DNAPL) Source Remediation concluded that the decision‐making process for implementing source depletion is hampered by quantitative uncertainties and that few useful predictive tools are currently available for evaluating the benefits. This article provides a new planning‐level approach to aid the process. Four simple mass balance models were used to provide estimates of the reduction in the remediation time frame (RTF) for a given amount of source depletion: step function, linear decay, first‐order decay, and compound. As a shared framework for assessment, all models use the time required to remediate groundwater concentrations below a particular threshold (e.g., goal concentration or mass discharge rate) as a metric. This value is of interest in terms of providing (1) absolute RTF estimates in years as a function of current mass discharge rate, current source mass, the remediation goal, and the source‐ reduction factor, and (2) relative RTF estimates as a fraction of the remediation time frame for monitored natural attenuation (MNA). Because the latter is a function of the remediation goal and the remaining fraction (RF) of mass following remediation, the relative RTF can be a valuable aid in the decision to proceed with source depletion or to use a long‐term containment or MNA approach. Design curves and examples illustrate the nonlinear relationship between the fraction of mass remaining following source depletion and the reduction in the RTF in the three decay‐based models. For an example case where 70 percent of the mass was removed by source depletion and the remediation goal (C_g/C₀) was input as 0.01, the improvement in the RTF (relative to MNA) ranged from a 70 percent reduction (step function model) to a 21 percent reduction (compound model). Because empirical and process knowledge support the appropriateness of decay‐based models, the efficiency of source depletion in reducing the RTF is likely to be low at most sites (i.e., the percentage reduction in RTF will be much lower than the percentage of the mass that is removed by a source‐depletion project). Overall, the anticipated use of this planning model is in guiding the decision‐making process by quantifying the relative relationship between RTF and source depletion using commonly available site data. © 2005 Wiley Periodicals, Inc.     

Chemical augmentation for the remediation of a hydrocarbon‐contaminated site

Field trials with inorganic fertilizer (nitrogen, phosphorus, and potassium) nutrients were simulated in the greenhouse to remediate hydrocarbon‐polluted soils from a spill site in the Niger Delta, Nigeria. Samples of the polluted soils taken from two depths were displayed in a randomized complete block (RCB) design and treated with 10–100 g of (NH₄)₂SO₄, KH₂PO₄, and KCl. The agronomic addition of the chemical nutrients was found to enhance the concentrations of nitrate‐nitrogen, phosphate‐phosphorus, and potassium in the soils. Pretreated nitrate‐nitrogen content ranged from 432 to 590 mg/kg in the polluted samples (with a control at 522 mg/kg), while posttreatment concentrations were 3,285 ± 154 mg/kg and 3,254 ± 159 mg/kg for surface and subsurface soils, respectively. © 2007 Wiley Periodicals, Inc.     

Utilization of nanoscale zero‐valent iron for source remediation—A case study

A pilot‐scale study was performed using a palladium‐catalyzed and polymer‐coated nanoscale zero‐valent iron (ZVI) particle suspension at the Naval Air Station in Jacksonville, Florida. A total of 300 pounds of nanoscale ZVI particle suspension was injected via a gravity feed and recirculated through a source area containing chlorinated volatile organic compounds (VOCs). The recirculation created favorable mixing and distribution of the iron suspension and enhanced the mass transfer of sorbed and nonaqueous constituents into the aqueous phase, where the contaminants could be reduced. Between 65 and 99 percent aqueous‐phase VOC concentration reduction occurred, due to abiotic degradation, within five weeks of the injection. The rapid abiotic degradation processes then yielded to slower biological degradation as subsequent decreases in ‐elimination parameters were observed—yet favorable redox conditions were maintained as a result of the ZVI treatment. Post‐treatment analyses revealed cumulative reduction of soil contaminant concentrations between 8 and 92 percent. Aqueous‐phase VOC concentrations in wells side gradient and downgradient of the source were reduced up to 99 percent and were near or below applicable regulatory criteria. These reductions, coupled with the generation of innocuous by‐products, indicate that nanoscale ZVI effectively degraded contamination and reduced the mass flux from the source, a critical metric identified for source treatment. A summary of this project was recently presented at the US EPA Workshop on Nanotechnology for Site Remediation in Washington, D.C., on October 21–22, 2005. This case study supplied evidence that nanoscale zero valent iron, an emerging remediation technology, has been implemented successfully in the field. More information about this workshop and this presentation can be found at www.frtr.gov/nano/index.htm. © 2006 Wiley Periodicals, Inc.     

Isolation and Characterization of a <Emphasis Type="Italic">Burkholderia</Emphasis> sp. USM (JCM15050) Capable of Producing Polyhydroxyalkanoate (PHA) from Triglycerides,Fatty Acids and Glycerols

A consortium of microorganisms from oil polluted wastewater sample was cultivated to promote polyhydroxyalkanoate (PHA) accumulation before subjecting the mixed cultures to sucrose density gradient ultracentrifugation. This resulted in the fractionation of the bacterial cells according to their physical features such as size, morphology and/or densities. An isolate was identified as Burkholderia sp. USM (JCM15050), which was capable of converting palm oil products [crude palm kernel oil (CPKO), palm olein (PO), palm kernel acid oil (PKAO), palm stearin (PS), crude palm oil (CPO), palm acid oil (PAO) and palm fatty acid distillate (PFAD)], fatty acids and various glycerol by-products into poly(3-hydroxybutyrate) [P(3HB)]. Up to 70 and 60 wt% of P(3HB) could be obtained when 0.5%(v/v) CPKO and glycerol was fed, respectively. Among the various fatty acids tested, lauric acid followed by oleic acid and myristic acid gave the best cell growth and PHA accumulation. Compared to Cupriavidus necator H16, the present isolate showed better ability to grow on and produce PHA from various glycerol by-products generated by the palm oil industry. This study demonstrated for the first time an isolate that has the potential to utilize palm oil and glycerol derivatives for the biosynthesis of PHA.