Isolation and characterization of a novel bacterial strain from a Tris-Acetate-Phosphate agar medium plate of the green micro-alga Chlamydomonas reinhardtii that can utilize common environmental pollutants as a carbon source

Background: Chlamydomonas reinhardtii, a green micro-alga can be grown at the lab heterotrophically or photo-heterotrophically in Tris-Phosphate-Acetate (TAP) medium which contains acetate as the sole carbon source. When grown in TAP medium, Chlamydomonas can utilize the exogenous acetate in the medium for gluconeogenesis using the glyoxylate cycle, which is also present in many bacteria and higher plants. A novel bacterial strain, LMJ, was isolated from a contaminated TAP medium plate of Chlamydomonas. We present our work on the isolation and physiological and biochemical characterizations of LMJ. Methods: Several microbiological tests were conducted to characterize LMJ, including its sensitivity to four antibiotics. We amplified and sequenced partially the 16S rRNA gene of LMJ. We tested if LMJ can utilize cyclic alkanes, aromatic hydrocarbons, poly-hydroxyalkanoates, and fresh and combusted car motor oil as the sole carbon source on Tris-Phosphate (TP) agar medium plates for growth. Results: LMJ is a gram-negative rod, oxidase-positive, mesophilic, non-enteric, pigmented, salt-sensitive bacterium. LMJ can ferment glucose, is starch hydrolysis-negative, and is very sensitive to penicillin and chloramphenicol. Preliminary spectrophotometric analyses indicate LMJ produces pyomelanin. NCBI-BLAST analyses of the partial 16S rRNA gene sequence of LMJ showed that it matched to that of an uncultured bacterium clone LIB091_C05_1243. The nearest genus relative of LMJ is an Acidovorax sp. strain. LMJ was able to use alkane hydrocarbons, fresh and combusted car motor oil, poly-hydroxybutyrate, phenanthrene, naphthalene, benzoic acid and phenyl acetate as the sole carbon source for growth on TP-agar medium plates. Conclusions: LMJ has 99.14% sequence identity with the Acidovorax sp. strain A16OP12 whose genome has not been sequenced yet. LMJ’s ability to use chemicals that are common environmental pollutants makes it a promising candidate for further investigation for its use in bioremediation and, provides us with an incentive to sequence its genome.


Introduction
Our research laboratory primarily focuses on the functional genomics of eukaryotic oxygenic photosynthesis using the model green micro-alga, Chlamydomonas reinhardtii. The work in this article stemmed from a side research project of four undergraduates from the University of West Georgia and, one high school student from the Carrollton High School in Georgia. This undergraduate/high school student research project was centered on minimizing bacterial contamination of C. reinhardtii in our research lab.
Chlamydomonas can be grown at the lab heterotrophically or photo-heterotrophically at room temperature in Tris-Phosphate-Acetate (TAP) medium, which contains acetate as the sole carbon source 1 . When grown in TAP medium, Chlamydomonas can utilize the exogenous acetate to synthesize glucose using the glyoxylate cycle, without being dependent on photosynthesis for glucose biosynthesis 2 . Aerobic bacteria can also utilize glyoxylate cycle to metabolize fatty-acids or two carbon-compounds such as acetate to synthesize oxaloacetate, which can be used for gluconeogenesis 3,4 . The acetate in the TAP medium can be substituted with alternative carbon sources to test if bacteria can use the tested chemicals as the sole alternative carbon and energy source.
We isolated a bacterial strain from a contaminated Chlamydomonas TAP-agar medium culture plate. This bacterium was named LMJ, after the abbreviated name of the Chlamydomonas strain it contaminated: LMJ.SG0182. We performed growth analyses and several microbiological tests on LMJ. LMJ grows faster on TAP medium than on lysogeny broth (LB) medium, is a mesophilic, non-enteric, gram-negative bacillus. LMJ does not grow on Mannitol Salt Agar (MSA) and MacConkey agar (MAC) and is sensitive to 1% NaCl. LMJ is starch hydrolysisnegative, gamma hemolytic and is oxidase-positive.
LMJ has a light pinkish-brown color on LB agar and creamy white color on TAP agar. We have found that on TAP + 1% tryptone medium plates in light, LMG colonies are pinkish brown pigmented, unlike that on the TAP-agar medium plates, indicating tryptone ingredients give the pinkbrown color to LMJ on TAP+1% tryptone medium. Preliminary spectrophotometric analyses of the pigment/chemicals exuded by LMJ indicate that the light pink-brown pigment is pyomelanin. Pyomelanin is an auto-oxidized and self-polymerized product of homogentisate (HGA), which is an important intermediate in the tyrosine catabolic pathway 5 . Pyomelanin is one of the many forms of melanin that is produced by bacteria, fungus and other organisms 5-10 . Generation of pyomelanin can provide a survival advantage, scavenge free radicals, bind various drugs, offer protection against light and reactive oxygen species, and is involved in iron reduction and acquisition, and extracellular electron transfer 11-17 .
We have amplified and sequenced partially LMJ's 16S rRNA gene. The best hit identified via the NCBI-BLAST analyses of the partial 16S rRNA gene sequence of LMJ is that of an uncultured bacterium clone LIB091_C05_1243 (Accession #: JX086489.1). We have submitted the partial 16S rRNA sequence of LMJ to the GenBank with the definition: Bacterium strain clone LIB091_C05_1243 variant 16S ribosomal RNA gene, partial sequence (Accession number: MN633292.1). The nearest relative of LMJ with a genus name is Acidovorax sp. strain A16OP12 (Accession #: MN519578.1).
Betaproteobacteria are highly metabolically diverse and contain chemolithoautotrophs, photoautotrophs, generalist heterotrophs and opportunistic pathogens. Acidovorax is a genus of betaproteobacteria of the order Burkholderiales and family Comamonadaceae 18,19 . Strains classified as Acidovorax have been associated with soils, wastewater treatment plants, plants, and clinical samples [20][21][22][23][24][25][26][27][28] . Reflecting the diversity inherent in this widespread distribution, isolates within this diverse genus have been linked to a variety of phenotypes ranging from plant pathogenicity, to denitrification, to the biodegradation of contaminants 29 .
Acidovorax sp. can degrade alkanes, polyhydroxyalkanoates (PHA) and polycyclic aromatic hydrocarbons (PAH) [30][31][32][33][34][35][36][37][38] . We tested the growth of LMJ on Tris-Phosphate (TP)-agar medium containing PAH, PHA, other aromatic compounds, cyclic alkanes and 10W30 car motor oil to determine if LMJ can use these compounds as the sole carbon source. LMJ was able to use cyclohexyl chloride, phenanthrene, naphthalene, benzoate, phenyl acetate and fresh and combusted 10W30 car motor oil. The abovementioned chemicals occur as common environmental pollutants in soil and water. In future, whole genome sequencing of LMJ and proper quantitative assays to determine LMJ's ability to degrade (and remove) toxic chemicals from the TP-growth medium are needed to probe its full potential for usage in environmental bioremediation. In this primarily undergraduate and high school student-driven research project, we are presenting our research on the isolation and physiological and biochemical characterizations of the novel bacterial strain, LMJ.

Growth media and cultures
We used the Chlamydomonas wild type strain 4A+ (CC-4051 4A+ mt+) strain in our antibiotic-sensitivity testing experiments. 4A+ strain was maintained on TAP agar medium in dim light intensities (1520 µmol m -2 s -1 ) at 22°C. Liquid 4A+ cultures were grown in 50 mL flasks in 15 mL of TAP in low light (50-80 µmol m -2 s -1 ) for 3 days. LMJ bacterial strain was maintained in the lab under dim light at 22°C on either TAP or LB agar medium plates. Liquid cultures of LMJ were grown in culture tubes in 3 mL of TAP or LB medium. 4A+ and LMJ liquid cultures were shaken at 150 rpm for aeration on a MaxQ420HP incubator shaker (Thermo Fisher Scientific, Waltham, MA). Light intensities were measured using a LI-250A light meter (LI-COR, Inc., Lincoln, NE).
The detailed protocol utilized to produce the TAP and TP medium used in this article is available from Protocols.io: https:// doi.org/10.17504/protocols.io.bgzujx6w.
LMJ growth analyses a) Testing salt-sensitivity of LMJ: LMJ was streaked on LB, TAP, LB-1% NaCl and TAP +1% NaCl agar medium plates. Streaked LMJ media plates were incubated either 22°C or at 37°C for 3 days and then imaged. b) Testing bile salts-/salt-sensitivity and ability to ferment lactose/mannitol: Growth assays on MAC and MSA were performed by streaking LMJ on MAC and MSA plates purchased from Carolina Biological (Burlington, NC). Media plates were incubated at room temperature for 4 days and then imaged to capture the LMJ growth and the pH change in the media. Escherichia coli and Staphylococcus aureus was used as a positive control for the MAC and the MSA experiment, respectively. c) Testing LMJ's ability to use different sugars as a sole carbon source: LMJ was streaked on agar plates containing TP-phenol red medium (pH 7.2) supplemented with 1% glucose, 1% sucrose and 1% lactose, respectively. Media plates were imaged after 5 days of growth at 22°C to capture the LMJ growth and the pH change in the media. d) Testing LMJ's ability to use different hydrocarbons and aromatic compounds as a sole carbon source: TP-agar plates were coated with different doses of cyclohexyl chloride, phenanthrene, naphthalene, benzoic acid, phenyl acetate and fresh and combusted 10W30 oil, using a modified technique 39 . 1% stock solutions of all chemicals (except 10W30 motor oil) were prepared by either dissolving or diluting the chemicals in chloroform. 10W30 fresh and used motor oils were diluted in chloroform to make a 2% (v/v) stock solution. 4 mL of 1% cyclohexyl chloride and 1% polyhydroxybutyrate (PHB) were coated on a TP plate. 2 mL and 4 mL of 1% phenanthrene stock solution were coated on TP plates. 0.5 mL, 1 mL and 2 mL of 1% napthalene, 1% benzoate and 1% phenyl acetate and 2% combusted and fresh 10W30 car motor oil were coated on TP plates. LMJ was streaked on the chemical-coated TP plates and incubated at room temperature. After 2 weeks, the plates were imaged using a Samsung Galaxy S5 camera. Images of all medium plates are available as Underlying data 40 .
Gram staining, oxidase test and starch hydrolysis test a) Gram staining: LMJ from LB-agar plate and LB and TAP shaking liquid cultures were used for Gram staining. Gram staining was performed using standard Gram staining protocol using Gram stain reagents from VWR (Radnor, PA). Gram-stained cells were viewed under oil immersion lens with a X100 magnification. Images of gram-stained cells were taken by a Samsung Galaxy S5 camera using a cell phone adapter for the microscope eyepiece. b) Oxidase test: Oxidase test was performed using Difco DrySlide Oxidase Disposable Slide purchased from Carolina Biological (Burlington, NC). The dry slide contains a film coated with an oxidase reagent (tetramethyl-p-phenylenediamine dihydrochloride). LMJ and Microbacterium sp. cells were taken from tryptic soy agar medium plates which does not contain any fermentable sugar. Fermentable sugars generate acid which can drop the pH below 5.1 and can give a false negative oxidase test result (https://microbeonline.com/oxidase-test-principle-procedure-and-oxidase-positive-organisms/) (Carolina Biological, Burlington, NC). Cells were streaked on the dry slide in two separate reaction areas. After 10 seconds, the color of the streak was captured with a Samsung Galaxy S5 camera.
c) Starch hydrolysis test: Starch hydrolysis test was performed on Mueller-Hinton-agar medium plates purchased from Carolina Biological (Burlington, NC). LMJ and E. coli were streaked on Mueller-Hinton agar medium plates and incubated for 48 hours at 37°C. After 48 hours of growth, plates were imaged. After imaging, Mueller-Hinton agar plates were flooded with Gram iodine and incubated for 10 minutes to test for the absence or presence of starch in the medium and the plate was re-imaged.
Antibiotic susceptibility test using disc diffusion method We modified the Kirby-Bauer (KB) disc diffusion method to perform the antibiotic susceptibility tests on TAP-agar plates (https://www.asm.org/Protocols/Kirby-Bauer-Disk-Diffusion-Susceptibility-Test-Pro). We grew LMJ in 3 mL of liquid TAP or in liquid LB and diluted the overnight culture 5-fold with liquid medium. The optical density of the 5-fold diluted culture was measured at 600 nm with a Beckman Coulter DU 730 Life science UV/Vis spectrophotometer (Brea, CA) 41 . The optical density of culture was adjusted with liquid medium to achieve an optical density of 0.08-13 which matches the 0.5 McFarland standard. Chlamydomonas strain 4A+ was grown in liquid TAP for three days and the optical density of the Chlamydomonas culture was measured at 750 nm with a Beckman Coulter DU 730 Life science UV/Vis spectrophotometer (Brea, CA) 42 . Measurement at 750 nm avoids the absorption of light by cellular pigments (chlorophyll and carotenoids) and is treated as a pure light scattering measurement 42 . The optical density of the Chlamydomonas culture was adjusted with TAP medium to achieve an optical density of 0.3-0.4.
Using a sterile swab, optical density-adjusted cultures of LMJ and Chlamydomonas were plated on the TAP plates. Two sterile filter paper discs were placed on each TAP plate with a separating distance of 4-5 cm. On one disc 50 µg or 100 µg of the antibiotic in a 20 µL total volume and on the other disc, 20 µL of sterile water was added (control). Antibiotics that were applied were: penicillin; neomycin, chloramphenicol and polymyxin B. Antibiotic plates were incubated at room temperature for 3-4 days. LMJ and Chlamydomonas plates were imaged after 3 and 4 days of incubation respectively, as Chlamydomonas grows slowly than bacteria. Diameters of zone of inhibitions were measured using a ruler. Standard deviations and means were calculated using Excel and, statistical analyses of the data from three biological replicates per experiment were performed using Microsoft Excels' t-Test: Paired Two Sample for Means tool in the analysis ToolPak. Both One-Tailed and Two-Tailed Hypothesis Tests were performed. Statistical analyses 43 and images of all antibiotic plates 44 are available as part of the Underlying data.
Analyses of pigment/chemicals of LMJ LMJ from TAP-agar plates were streaked on fresh TAP +1% tryptone-agar plates. One plate was incubated under light intensity of 350 µmol photons m -2 s -1 and the other plate was kept in dark at 22°C. Images of the plates were taken after 3 days of growth to monitor pigment production. LMJ cells were treated in three different ways for spectrophotometric analyses. 1) LMJ was grown in 2.5 mL of LB medium at 37°C for 3 days. 2 mL of the LB culture was centrifuged at 5000 X g for 2 minutes. The supernatant and the cell pellet were collected. Supernatant was alkalinized (20 µL of 6 M NaOH per ml of sample) and centrifuged at 16,000 X g for 2 minutes and the supernatant was collected. 2) LMJ cell pellet from treatment 1 was resuspended in 200 µL of 1% NaNO 2 solution and 1mL of 0.1N-HC1 by vortexing the sample for few minutes and incubated for 5 minutes. 3) LMJ cells from a LB-agar medium plate was resuspended in 1 mL of 6M NaOH by vortexing and incubated for 5 minutes. Acidified and alkalinized tubes of cell pellet washes from treatments 2 and 3 were centrifuged at 16,000 X g for 2 minutes and the supernatants were collected separately.
Supernatants obtained from the above stated three treatments were filtered using a 5 mL syringe fitted to a nylon membrane filters with a cut-off of 0.45 µm. Pigment formation in the alkalinized supernatant from the liquid LB culture and, the alkalinized-and acidified-supernatants from cell pellet washes were analyzed by using the wavelength scan program ranging 200 -600 nm in a Beckman Coulter DU 730 Life science UV/Vis spectrophotometer (Brea, CA). To detect pyomelanin in the supernatant of the LB liquid culture, the absorption peak at the 400 -405 nm region was monitored. To detect homogentisate (HGA) in the alkalinized supernatant from the cell pellet wash, the absorption peak at the 290 nm was monitored. To detect 1:4-benzoquinone-2-acetic acid (benzoquinone acetate; BQA), the absorption peak at the 250 nm was monitored in the acidified supernatant obtained from the cell pellet wash. Our protocol is a "quick and crude" version of the protocol available in the literature for preparation of samples for spectrophotometric assays of pyomelanin, BQA and HGA [45][46][47] .
Genomic DNA isolation and PCR amplification of the partial 16S rRNA gene Genomic DNA was isolated using Qiagen's blood and cell culture DNA mini kit (Qiagen, Valencia, CA) according to the protocol given in the technical manual. DNA concentration and purity of the isolated genomic DNA sample were measured using a Nanodrop 2000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA). Genomic DNA sample was separated on a 1% agarose gel and the quality of the sample was visualized by imaging the gel with a BioRad Molecular Imager Gel Doc XR+ (BioRad, Hercules, CA).
Forward and reverse 16S rRNA PCR primers were designed based on sequences in the literature for selecting primer pairs with the best overall coverage and phylum spectrum to reduce the bias in PCR-based microbial diversity studies 48 . The sequence of the forward primer 16SF is: 5' CCTACGGGNGGCWGCAG 3' and that of the reverse primer 16SR is: 5' GACTACHVGGG-TATCTAATCC 3'. HotStar Taq Plus DNA polymerase enzyme kit (Qiagen, Valencia, CA) was used for PCR following the given cycling conditions given in the Qiagen protocol booklet.
Gel extraction of the 16S rRNA amplicon and its cloning The PCR-amplified partial 16S rRNA genomic product was excised from the agarose gel and purified using the QIAquick Gel Extraction Kit (Qiagen, Valencia, CA). The purified PCR product was cloned using the TOPO TA cloning kit in the pCR4-TOPO TA vector (Thermo Fisher Scientific, Waltham, MA) according to the protocol given in the technical manual. One clone harboring the partial 16S rRNA gene of LMJ was sequenced by the UC Berkeley DNA Sequencing Facility. Chromas Lite and BLAST program were used to analyze DNA sequences. Raw electropherogram files and sequence text files are available as Underlying data 49 .

Isolation of the bacterial strain LMJ
We found a creamy white bacterial contamination on a Chlamydomonas strain, LMJ.SG0182 TAP plate at our laboratory. ( Figure 1A). We purified the bacterial strain using the streak plate method to isolate single bacterial colonies on fresh TAP medium plates. We picked ten single colonies and transferred them to a LB agar medium plate ( Figure 1B). Colony # 10 was selected for our studies ( Figure 1B). Colony # 10 was streaked on fresh LB and TAP-agar medium plates to maintain the purified bacterial strain in the lab ( Figure 1C, D). We named this bacterial strain as LMJ after the abbreviated name of the Chlamydomonas strain LMJ.SG0182, as it was isolated from this Chlamydomonas strain's culture plate. LMJ is an acid-devouring strain as it was able to grow on the TAP-agar medium ( Figure 1D). LMJ culture on LB agar medium appears pigmented with a light pinkish-brown color ( Figure 1C) but on TAP agar medium the culture is creamy white ( Figure 1D).
TAP medium can be used as a new stringent minimal medium for LMJ TAP medium recipe can be found at the website of Chlamydomonas Resource Center. Hutner's trace element solution is an ingredient in the TAP medium. Hutner's trace element recipe can be found at https://www.chlamycollection.org/methods/media-recipes/hutners-trace-elements/. M9 medium is the standard minimal medium for growing bacteria. In our lab we use a slightly modified TAP medium recipe which has a final concentration of phosphate, nitrogen, magnesium and calcium approximately 10-fold, 2-fold, 2-fold and 2-fold higher than that in the TAP recipe found on the Chlamydomonas Resource Center website, respectively. Final concentrations of acetate and Hutner's trace elements are the same in both TAP recipes. Table 1 compares the chemical ingredients in our lab's TAP recipe with that present in the standard M9 medium described at http://www.thelabrat.com/protocols/m9minimal.shtml. M9 medium has a final concentration of phosphate, nitrogen, magnesium and carbon in the medium approximately 70-fold, 2.5-fold, 4-fold and 5-fold higher than that present in our lab's TAP medium, respectively. Additionally, M9 contains 0.05% salt (8.56 mM) ( Table 1). TAP has additional trace elements like iron, zinc, copper, manganese,  Table 1. Comparison of chemical ingredients in the TAP and in M9 growth media. TAP medium is used for growing Chlamydomonas heterotrophically or photo-heterotrophically. M9 medium is the standard minimal medium for growing bacteria. Note: Hutner's trace element is an ingredient in the TAP medium. TAP trace elements and EDTA shown in the table are components in the Hutner's trace element solution. pH of Hutner's solution is adjusted to 6.5 using KOH (not NaOH) pellets before it is used to make the TAP medium. Both growth media have (pH 7-7.2). Acetate in the TAP medium can be substituted with alternative carbon sources. TAP medium minus acetate is the TP medium in our work and the media recipes can be found at https://doi.org/10.17504/protocols.io.bgzujx6w.

Chemical
Final Gram staining Gram staining of LMJ cells from a LB-agar medium plate revealed that LMJ cells are straight to slightly curved rods ( Figure 2). Cells occur singly, in pairs or in short chains. LMJ is a gram-negative bacterium ( Figure 2).

Analyses of LMJ growth on TAP-and LB-agar medium plates at different temperatures
We have monitored the growth of LMJ on LB-agar, TAP-agar and Mueller-Hinton agar medium over 5 days. LMJ has less dense growth on LB agar than on TAP agar or on Mueller-Hinton agar at 22°C ( Figure 3A, B, E). LMJ has dense growth at 37°C than at 22°C on all three media tested ( Figure 3C, D, F). It is to be noted that LMJ appears lightly pigmented on both LB-agar and Mueller-Hinton agar but not on TAP-agar ( Figure 1C and Figure 3C, E, F).

Salt-sensitivity of LMJ
LMJ grows on the nutrient-rich LB agar medium slowly compared to that on the TAP agar medium ( Figure 3). TAP does not contain NaCl (Table 1) but LB medium has 1% NaCl (http://2018.igem.org/wiki/images/f/f2/T--Toronto--_LB_ Medium_Preperation_Protocol.pdf). Gram-negative bacteria are usually sensitive to salt. Hence, we studied the growth of LMJ on LB, LB -1% NaCl, TAP, and TAP +1% NaCl-agar medium at 22°C and at 37°C. LMJ grew faster on LB-1% NaCl agar compared to that on the LB agar at both temperatures ( Figure 4A-D). LMJ grew very slowly on TAP +1% NaCl agar compared to that on the TAP-agar at both temperatures ( Figure 4E-H). The slow growth of LMJ was very pronounced at 22°C than at 37°C on both LB-agar and TAP +1% NaCl-agar medium ( Figure 4A, C, E, G). Taken together, our results show that LMJ is sensitive to even 1% of NaCl in LB that is tolerated well by many Gram-negative bacteria.
Liquid medium grown-LMJ cells are prone to cell lysis during Gram staining In Figure 2, LMJ cells from a LB-agar medium plate was used for Gram staining. We performed Gram staining using cells from LMJ liquid TAP and liquid LB cultures that were shaking in an incubator shaker at 150 rpm at 37°C ( Figure 5). Although the turbidity of the TAP or the LB liquid culture indicates dense growth ( Figure     Underlying data 50 ). We have monitored the LMJ LB and liquid culture growth over a period 96 hours and we did not see any clearing of the TAP and LB liquid cultures (see Underlying data 50 ). Cells from the liquid TAP culture were plated on a fresh TAP-agar medium plate and LMJ grew back within 4 days at room temperature (see Underlying data 50 ). Cells in liquid culture were not dead although we saw mainly cell debris and very few intact cells after gram staining. Taken together, our results indicate that LMJ is probably a biofilm forming bacteria. It could not form biofilm in a shaking liquid culture and cells were prone to lysis in the shaking liquid culture (see Discussion).

Pigment studies
Many bacteria are known to produce a brown-black melanin pigment called pyomelanin 5,17 . Light and oxygen are needed for the formation of pyomelanin 45 . Aromatic amino acid tyrosine is needed for pyomelanin formation 5 . Phenylalanine can also contribute to the synthesis of pyomelanin as it can be can be converted to tyrosine by the enzyme phenylalanine-4-hydroxylase 51 . LB medium contains 1% tryptone which is a rich source of different amino acids including the aromatic amino acids (https://khimexpert.com/wp-content/uploads/2018/12/GCM23-Tryptone.pdf).
We tested if the light brown color of LMJ on LB medium is because of tryptone which provides aromatic amino acids.
We grew LMJ on TAP +1% tryptone-agar medium plates in dark and in light. In the dark, on TAP + 1% tryptone medium plate LMJ did not appear to be pigmented, unlike that in the light ( Figure 6). We found that 1% tryptone and light are needed for pigment production in LMJ ( Figure 6). Pyomelanin is a negatively charged extracellular pigment of high molecular weight, derived from the tyrosine catabolism pathway 11 (Figure 7). Pyomelanin is usually produced because of defects in the tyrosine catabolism pathway that leads to an accumulation of homogentisate (HGA) and occurs naturally in many pyomelanin over-producing strains 5,52 (Figure 7). Accumulation of HGA can occur because of an inactivation of the enzyme homogentisate 1, 2 dioxygenase (HmgA) 52,53 (Figure 7). Accumulated HGA is secreted out of the cells by an ABC transporter and is auto-oxidized to 1:4-benzoquinone-2-acetic acid (benzoquinone acetate; BQA) and then polymerized to form the brown pigment pyomelanin (Figure 7). We wanted to see if we can detect HGA, BQA and pyomelanin in the alkalinized LMJ LB liquid culture medium and in the acidified and alkalinized LMJ cell pellet-wash supernatants [45][46][47] .
Pyomelanin absorption peak is between 400 and 405 nm [45][46][47] . We observed a 402 nm absorption peak in the absorption curve of alkalinized LMJ liquid LB culture medium ( Figure 8A). BQA absorbs maximally in the UV region at 250 nm 45 . We observed an absorption peak at 252 nm in the absorption curve of acidified-cell pellet wash supernatant derived from LMJ liquid LB culture ( Figure 8B). HGA absorbs maximally in the UV region at 290 nm 45 . We observed an absorption peak at 291 nm in the absorption curve of alkalinized cell pellet wash supernatant derived from LMJ cells from a LB-agar medium plate ( Figure 8C). A slight 1-2 nm shift was observed in the HGA and BQA absorption peaks in our samples compared to the values found in literature (see Discussion) 45 . Taken together our results strongly indicate the LMJ produces pyomelanin and its production is stimulated under light by tryptone ( Figure 6 and Figure 8). We did not have tyrosine at the time of submission of this work.
LMJ growth on MAC and MSA MAC is a selective and differential medium used for isolation and differentiation of enteric gram-negative bacteria based on their ability to ferment lactose. Bile salts and crystal violet in MAC  inhibit the growth of gram-positive bacteria. Lactose in MAC is a source of fermentable carbohydrate. Neutral red is a pH indicator present in MAC that turns red at a pH below 6.8 and is colorless at a pH greater than 6.8. Bacteria that ferment lactose and thereby produce acid in the medium will appear pink because of the neutral red turning red while bacteria that are lactose non-fermenters will produce normal-colored or colorless colonies. LMJ was unable to grow on MAC ( Figure 9A; right) unlike E. coli, a gram-negative enteric bacterium ( Figure 9A; left). E. coli appeared pink on MAC plate, indicating it can ferment lactose ( Figure 9A; left). Additionally, bile salts precipitated out of the MAC medium surrounding the growth of E. coli because of the acidic pH ( Figure 9A; left). Our results indicate that LMJ is a non-enteric bacterium. Inability of LMJ to grow on MAC could be because: 1) LMJ cannot use lactose as a carbon/energy source; 2) because it is sensitive to bile salts and crystal violet in the MAC medium or 3) a combination of 1 and 2.
MSA is a selective and differential medium. MSA contains a high concentration (about 7.5-10%) of NaCl. This makes MSA selective for many high salt-tolerant gram-positive bacteria (Staphylococcus, Enterococcus and Micrococcus) as the high salt concentration is inhibitory for growth of most bacteria. MSA also contains the sugar mannitol and the pH indicator phenol red. If a bacterium can ferment mannitol to acid, the color of phenol red in the agar will change from red to yellow. LMJ being gram-negative and salt-sensitive (Figure 2 and Figure 4), fails to grow on MSA ( Figure 9B, right) while Staphylococcus aureus, a mannitol-fermenter, grew on MSA and produced acid that changed the phenol red's color to yellow ( Figure 9B, left).

Ability of LMJ to use different sugars as an alternative carbon source
We grew LMJ on TP + 1% sugar agar which contained phenol red as the pH indicator. We replaced the carbon source acetate in the TAP medium with sugars like glucose, sucrose and lactose ( Figure 10). TAP minus acetate medium is called TP medium in this work. Figure 10A, Figure 10C and Figure 10E represent control TP + 1% glucose, TP + 1% sucrose and TP + 1% lactose plates, respectively. LMJ grew very well on TP + 1% glucose agar and fermented glucose to produce acid ( Figure 10B). It did grow to some extent on TP +1% sucrose agar but not as well as it did on the TP +1% glucose agar ( Figure 10B, D). It was hard to confirm if LMJ fermented sucrose to any significant degree as there was no distinct color change of phenol red like that in Figure 10B ( Figure 10D). But it is to be noted that the color of phenol red in the control TP +1% sucrose agar was light red ( Figure 10C) and that on LMJ-TP +1% sucrose agar was light orange ( Figure 10D), indicating there could have been some sugar fermentation. No visible growth of LMJ was observed on TP +1% lactose agar. Taken together with results from the LMJ growth on MAC medium ( Figure 9A), LMJ cannot use the disaccharide lactose as a carbon source ( Figure 9A and Figure 10F) but can use monosaccharide glucose and disaccharide sucrose as alternative carbon sources ( Figure 10B, D).

Starch hydrolysis test
Starch hydrolysis test is used to identify bacteria that can hydrolyze starch (amylose and amylopectin) using the enzymes α-amylase and oligo-1,6-glucosidase. Because of the large size, amylose and amylopectin molecules cannot cross the bacterial cell wall. To use starch as a carbon source, bacteria must secrete α-amylase and oligo-1,6-glucosidase into the extracellular space. These enzymes break the starch molecules into smaller glucose subunits which can be utilized by the cells. To interpret the results of the starch hydrolysis test, Gram iodine was added to the agar. Iodine reacts with the starch to form a dark brown/blue color. Hydrolysis of starch will create a clear zone around the bacterial growth. Both LMJ ( Figure 11B) and E. coli ( Figure 11D) tested negative in the starch hydrolysis test as there was no clear zone around the growth on the Mueller Hinton agar. We did not have an access to a starch-positive strain to use as a positive control in the starch hydrolysis test.

Oxidase test
The oxidase test is used to identify aerobic, facultative anaerobic or microaerophilic bacteria that produce cytochrome c oxidase, an enzyme of the electron transport chain. When present, cytochrome c oxidase oxidizes the oxidase reagent (tetramethyl-p-phenylenediamine; TMPD) to indophenols (purple colored product) within 5-10 seconds. When the enzyme is not present, the reagent remains reduced and is colorless. Oxidase-positive strains take 5-10 seconds to form indophenols and the color change occurs within 30 seconds. Delayed oxidase-positive strains form indophenols within 60-90 seconds and oxidase-negative strains can either remain colorless or take more than 2 minutes to show the purple color because of slow spontaneous non-enzymatic oxidation of TMPD in air (https://www.asm.org/Protocols/Oxidase-Test-Protocol). Our oxidase test results show that LMJ is oxidase-positive (Figure 12; left) and Microbacterium sp. is oxidase-negative ( Figure 12; right). Hence LMJ is an aerobic bacterium and uses cytochrome c in the electron transport chain (Figure 3-Figure 6, Figure 8 and Figure 12).
Testing of antibiotic-sensitivity of Chlamydomonas and LMJ to identify an antibiotic that will eliminate LMJ contamination of Chlamydomonas We tested four antibiotics to determine which of these four antibiotics and at what dose, will be effective in inhibiting growth of LMJ with no/minimal detrimental effect on Chlamydomonas growth. In the first set of experiments, we determined the antibiotic-sensitivity of LMJ and Chlamydomonas 4A+ strain separately to identify the effective antibiotic and, the required dose. In the second set of experiments, we streaked Chlamydomonas and LMJ together on the TAP-agar medium plate containing the antibiotic with the effective dose that we found to be potent against LMG (without hindering Chlamydomonas growth) from the first experiment. This was done to confirm that the selected antibiotic is effective in eliminating LMJ contamination on Chlamydomonas TAP-agar plates.
We modified the traditional KB disc diffusion method to test for antibiotic-sensitivity as described under Method section. We tested two different doses (50 µg and 100 µg) of penicillin, polymyxin B, neomycin and chloramphenicol. Table 2 shows the average diameter of the zone of inhibition for each antibiotic dose, with the standard deviations. Statistical analyses are available as part of the Underlying data 43 . Images of all antibiotic plates are available as Underlying data 44 .   (on the right) streaked on a disposable slide containing a film coated with oxidase reagent (tetramethyl-p-phenylenediamine dihydrochloride). Image of the slide was taken after 10 seconds of the application of the cells on the slide. LMJ is cytochrome c oxidase-positive as cytochrome c oxidase, if present, oxidizes the oxidase reagent on the film to form purple colored-indophenols. Microbacterium sp., a yellowpigmented bacterium, is oxidase-negative and fails to form the purple-colored product. Cells were taken from strain specific-tryptic soy agar medium plates.  any zone of inhibitions (Table 2). LMJ was highly sensitive to penicillin (Table 2), despite being a gram-negative bacterium. p-values for the one-tailed and two-tailed hypothesis test for both doses were infinitely small and statistically significant.
To ensure that the penicillin-sensitivity of LMJ is not because of the TAP-agar medium used in our experiments, we tested penicillin-sensitivity of LMJ and E. coli (control) on LB-agar medium and LB-1% NaCl agar medium using 50 µg and 100 µg of penicillin ( Figure 13). We found that LMJ did not grow on LB-agar in the presence of penicillin ( Figure 13A, B). LMJ grew on LB-1% NaCl + penicillin plates and showed a prominent zone of inhibition like it showed on TAP-agar penicillin plates ( Figure 13C, D). E. coli was not sensitive to either of the two penicillin doses ( Figure 13E, F). We have shown in Figure 4A, E that 1% NaCl inhibits growth of LMJ at 22°C. Hence penicillin in combination with 1% NaCl completely prevented growth of LMJ on LB-agar + penicillin plates ( Figure 13A, B). We did not measure the diameter of the inhibition zones as this experiment was performed to compare penicillin sensitivity of two gram-negative bacteria, namely E. coli and LMJ on LB agar medium.

b) Polymyxin B-sensitivity testing:
Polymyxin B binds to the lipopolysaccharide of the outer membranes of gram-negative bacteria and increases the permeability of the bacterial outer membrane, which causes cell death. At 50 µg (500 IU) dose, LMJ is more sensitive to polymyxin B than Chlamydomonas ( Table 2). The p-values for the one-tailed and two-tailed tests for the 50-µg dose were 0.4% and 0.09%, respectively, indicating that the polymyxin B sensitivity of LMJ is statistically significant. The p-values for the one-tailed and two-tailed tests for the 100-µg dose were 6.4% and 12.9%, respectively indicating that there was no significant difference in polymyxin b-sensitivity between Chlamydomonas and LMJ (Table 2).
c) Neomycin-sensitivity testing: Neomycin inhibits protein translation by binding to the 30S subunit of bacterial ribosomes. At 50 µg dose, there was no statistically significant difference in neomycin-sensitivity between Chlamydomonas and LMJ as the p-values for the one-tailed and two-tailed tests for the 50 µg dose were 50% and 100%, respectively. At 100 µg dose, LMJ was more sensitive to neomycin than Chlamydomonas ( Table 2). The p-values for the one-tailed and two-tailed tests for the 100-µg dose were 0.2% and 0.5 % respectively, indicating that there was a significant difference in neomycin-sensitivity between Chlamydomonas and LMJ (Table 2). d) Chloramphenicol-sensitivity testing: Chloramphenicol inhibits protein synthesis by binding to the 50S subunit of bacterial ribosomes. Chlamydomonas was resistant to both 50 µg and 100 µg of chloramphenicol as it did not show any zone of inhibitions (Table 2). LMJ was highly sensitive to chloramphenicol compared to Chlamydomonas (Table 2). e) Testing the potency of penicillin and chloramphenicol in minimizing LMJ contamination on Chlamydomonas culture plates: Our first set of experiments determined penicillin and chloramphenicol are the best antibiotic choices for minimizing LMG contamination. We tested combined growth of LMJ and the wild type Chlamydomonas strain 4A+ on TAP agar plate containing 50 µg penicillin/mL of the medium ( Figure 14A) and on TAP-agar plate containing 50 µg chloramphenicol/mL of the medium ( Figure 14B). LMJ growth was not visible on both penicillin and chloramphenicol TAP plates ( Figure 14).
PCR amplification of the partial 16S rRNA gene of LMJ Figure 15A shows a schematic diagram of a full-length 16S rRNA gene based on the E. coli 16S rRNA gene.  Figure 15A). Figure 15B shows that PCR amplification of the partial 16S rRNA gene generated an amplicon of approximately 460 bp in size ( Figure 15A).
NCBI-BLAST analyses of the 16S rRNA partial gene sequence of LMJ The amplicon shown in Figure 15B was sequenced to determine the nearest relative of LMJ. NCBI-nucleotide BLAST analyses identified the best match to LMJ's 16S rRNA gene partial sequence as that of an uncultured bacterium clone LIB091_C05_ 1243 16S ribosomal RNA gene partial sequence (Accession #: JX086489.1). This hit had a score of 843; 0 E-value and percent identity of 99.35%. Figure 16A shows three nucleotide substitutions (transitions) that are present in LMJ 16S rRNA gene sequence relative to uncultured bacterial clone hit (altered nucleotide in LMJ is shown in red font). Two of these nucleotide substitutions are in the conserved regions, C2 (nucleotide position 348) and, C3 (nucleotide position 542) and the third nucleotide substitution is in the V4 region (nucleotide position 607) ( Figure 16A).
We found that the nearest relative of LMJ with a specific genus name is Acidovorax sp. strain A16OP12 16S (Accession #: MN519578.1). Acidovorax sp. hit had a score of 837, 0 E-value and 99.14% sequence identity. In addition to the above stated three nucleotide substitutions, a fourth nucleotide substitution (another transition at nucleotide position 798) within the 11 bp invariant region in the C4 region was observed, when LMJ's partial 16S rRNA sequence was compared with that of the Acidovorax sp. strain A16OP12 (Accession #: MN519578.1) ( Figure 16B). We have deposited the partial 16S rRNA sequence of LMJ in GenBank with the definition: Bacterium strain clone LIB091_C05_1243 variant 16S ribosomal RNA gene, partial sequence (Accession number: MN633292.1). Raw electropherogram files and sequence text files are available as Underlying data 49 .
Ability of LMJ to use PAHs, saturated hydrocarbons and PHA as the sole carbon source Acidovorax sp. utilize alkanes, PAH and PHA as alternative carbon sources for growth 30-38 . Since the nearest relative of LMJ is Acidovorax, we tested if LMJ can utilize the above mentioned chemical compounds as a carbon source for growth. TP medium (lacks a carbon source) was supplemented with the following three different categories of external carbon sources in separate experiments: 1) saturated alkane hydrocarbons, 2) aromatic compounds (includes PAH) and, 3) PHA: PHB. Images of all medium plates are available as Underlying data 40 .   a) Testing hydrocarbons (cycloalkanes and 10W30 oil) as the sole carbon source: LMJ was streaked on TP-agar plate as a control to show that LMJ does not grow on a TP medium plate ( Figure 17A). 1% cyclohexyl chloride ( Figure 17B), 2% (v/v) fresh 10W30 motor oil ( Figure 17C) and 2% (v/v) combusted 10W30 motor oil ( Figure 17D) were used as carbon sources. We tested one dose of 1% cyclohexyl chloride (4 mL) and three different doses (0.5, 1 and 2 mL) of the 2% (v/v) stock solutions of the fresh and combusted 10W30 motor oil. In Figure 17, we are presenting the results of use of only one dose (2 mL) per types of motor oil. LMJ can grow well on TP-agar media plates coated with 4 ml of 1% cyclohexyl chloride ( Figure 17B), and 2 mL of 2% fresh and 2% combusted 10W30 motor oil as a carbon source ( Figure 17C, D).
b) Testing PAH and other aromatic compounds as the sole carbon source: Phenanthrene and napthalene are PAHs. Anthropogenic releases of benzoic acid and sodium benzoate into the environment are primarily from their uses as preservatives.
Phenylacetate is found in the environment as a common carbon source and is a central intermediate in the degradation of many aromatic compounds such as phenylalanine, phenylacetaldehyde, 2-phenylethylamine and environmental contaminants like styrene and ethylbenzene 58 .
c) Testing PHB as the sole carbon source: PHB is a polymer belonging to the polyesters class (PHA) that are of interest as bio-derived and biodegradable plastics 32 . We tested one dose of  1% PHB (4 mL) on the TP-agar plate ( Figure 19). LMG can grow on TP + PHB agar but it grows slowly ( Figure 19).

Discussion
LMJ is a mesophilic, acetate-loving, pigmented, gram-negative rod. It is a salt-sensitive, oxidase-positive, starch hydrolysisnegative, non-enteric bacterium (Figure 1-Figure 12). LMJ is gamma hemolytic (results available as Underlying data 59 ). NCBI-BLAST analyses of the partial 16S rRNA gene sequence of LMJ revealed that its best match is the partial 16S rRNA gene sequence of an uncultured bacterium clone LIB091_C05_ 1243 16S (Accession #: JX086489.1). The isolation source for this NCBI match is from monochloramine-treated drinking water biofilms 60 . The second best match to the LMJ's partial 16S rRNA gene sequence is that of Acidovorax sp. strain A16OP12. This Acidovorax strain is isolated from a lake sediment in China (NCBI, Accession #: MN519578.1).

Pseudomonas facilis, Pseudomonas delafieldii, E. Falsen (EF)
Group 13, EF Group 16, and several clinical/environmental isolates have been assigned a new genus name, Acidovorax, and belongs to the acidovorans (acid-devouring bacteria) rRNA complex in rRNA superfamily III (betaproteobacteria) in the family Comamonadaceae 19 . Members of these genera are aerobic, mesophilic, gram-negative, oxidase-positive rods, starch-hydrolysis-negative and are commonly found in biofilm communities in soil, water and on plants 61 . Pyrosequencing analysis of bacterial biofilm communities in a water meter of a drinking water distribution system in Illinois revealed that 58% of betaproteobacteria in the biofilm on the water meter were Acidovorax sp. 62 . Biofilm formation is essential for the virulence of phytopathogenic strains of Acidovorax species 24,25,27,63-65 .
Our results indicate that LMJ forms biofilm ( Figure 5).  Figure 18A served as the negative control for this experiment. Plate was imaged after two weeks of growth at room temperature.
Many bacteria produce extracellular and surface-associated components such as membrane vesicles, extracellular DNA and moonlighting cytosolic proteins for which the biogenesis and export pathways are not fully understood 66 . In Pseudomonas aeruginosa, cells undergo explosive cell lysis as a mechanism for the biogenesis of bacterial membrane vesicles and biofilm 66 . LMJ liquid cultures were inoculated with tooth picks ( Figure 5). We have noticed LMJ growth on the tooth pick that is immersed in the shaking liquid media. In future, we will gram-stain cells from non-shaking liquid cultures to compare with that from the shaking cultures.  Figure 13). In a KB test if the diameter of the zone of inhibition is more than 29 mm, with a 10-µg dose (16.5 IU units) of penicillin, then the bacteria is sensitive to penicillin (see Methods). We used penicillin doses that were 5-to 10-fold higher than what is usually used in a KB test. There is one report of a multipleβ-lactam-antibiotic-resistant Acidovorax sp. strain MR-S7 67 .
If the diameter of the zone of inhibition is more than 17 mm, with a 30-µg dose of chloramphenicol in a KB test, the bacterium is susceptible to chloramphenicol (https://www.flinnsci.com/antibiotic-sensitivity-disk-chloramphenicol-30-g/ab1400/). LMJ is sensitive to chloramphenicol but Chlamydomonas is resistant. If the diameter of the zone of inhibition is more than 16 mm, with a 30 µg dose of neomycin in a KB test, the bacterium is susceptible to neomycin (https://www.flinnsci.com/antibioticsensitivity-disks-neomycin-30-g/ab1403/). If the diameter of the zone of inhibition is more than 12 mm with the application of 300 IU of polymyxin B in a KB test, then the bacteria is sensitive to polymyxin B 68 . We used antibiotic doses of neomycin and polymyxin B were 1.7-to 3.3-fold higher than what is used for KB tests (Table 2). LMJ is resistant to neomycin and polymyxin B (Table 2). We have not found any studies to date that have tested the sensitivity of Acidovorax sp. to polymyxin B, neomycin and chloramphenicol.
Many phytopathogenic Acidovorax strains are pigmented 18 . LMJ has light pink-brown pigmentation. Pseudomonas aeruginosa has water soluble pinkish red pyorubrin pigment and dark brown pyomelanin pigment 69-71 . Pyorubrin's biosynthesis is enhanced by the addition of 1% DL-glutamate in the growth media 69 . Pyorubrin has a characteristic absorption peak in the visible light at 520 nm 70 . Pyomelanin is produced as a product of tyrosine catabolism via homogentisate (HGA) (Figure 7). Pyomelanin biosynthesis needs oxygen and light and can be enhanced by the addition of 0.36-1% tyrosine in the growth medium.
Pyomelanin has a characteristic absorption peak in the visible light ranging from 400-405 nm 46,47 .
We used 1% tryptone as we did not have access to tyrosine at our lab. Commercial tryptone contains 1.86 grams of tyrosine/100 grams of tryptone (https://khimexpert.com/wp-content/ uploads/2018/12/GCM23-Tryptone.pdf). The 1% tryptone contained 0.186 g of tyrosine/L of liquid medium which is approximately 19-to 54-fold lower than what researchers have used in inducing pyomelanin production in bacteria 47,69 . Although 1% tryptone induced pigment production in LMJ on TAP medium ( Figure 6) it was not dark brown like that observed in other bacterial or fungal strains 5,46,47 . In future, we plan to test the enhancement of pigment production in LMJ with the addition of 1% tyrosine in the growth media.
LMJ pigmentation on TAP+1% tryptone in light and in dark and spectrophotometric pigment analyses strongly indicate that the light pink-brown pigmentation in LMJ is due to light-induced HGA-based pyomelanin production ( Figure 6 and Figure 8).
In our experiments, we have a very small shift of 1-2 nm in the absorption peaks for BQA and HGA ( Figure 8B, C) because we did not buffer our samples to a pH of 6.7-6.8 with phosphate buffer 69 . We performed this experiment using a "quick and crude" protocol to get preliminary data before we optimize our experimental protocol according to the protocols found in the literature 45,47 . We plan to optimize our protocols for preparing the samples for the spectrophotometric analyses using the method described in the literature 69 . We would also like to test if the addition of ascorbic acid in the buffered-acidified cell pellet washes can reduce BQA back to HGA via monitoring the shift in absorption maxima from 250 to 290 nm, as described previously 69 .
Pyomelanin protects cells against oxidative stress 5,15 . It would be interesting to probe pyomelanin's role in oxidative stress protection in LMJ. LMJ growth can be monitored on TAP +1% tyrosine agar plate in the presence/absence of hydrogen peroxide and photo-sensitizers like Rose Bengal, that generates the reactive oxygen species, singlet oxygen, in the presence of light and oxygen 72 . Experiments can be performed in the absence and presence of inhibitors of 4-hydroxyphenylpyruvate dioxygenase (HPPD) which are herbicides like 2-[2nitro-4-(trifluoromethyl) benzoyl]-1,3-cyclohexanedione (NTBC) (Figure 7) 11,73 . Additionally, effects of different light intensities, pH, UV light, heat and salt stress on pyomelanin production can be determined.
Two and three nucleotide substitutions in the conserved regions of the 16S rRNA gene were observed in LMJ when compared with that of the uncultured bacterial clone LIB091_C05_1243 and Acidovorax sp. strain A16OP12, respectively ( Figure 16). These results show that conserved regions of the 16S rRNA are not really "conserved" and conserved regions of the 16S rRNA gene exhibit considerable variations that need to be considered, when using this gene as a biomarker 74 .
Different environmental strains of Acidovorax sp. exist that can degrade polychlorinated-biphenyls, PAH, plastic films and saturated hydrocarbons (alkanes) which are major environmental pollutants 30-38,75-79 . In our first preliminary round of experiments, presented in this work, we have shown that at 22°C on TP medium, LMJ can use PAH, aromatic acids/esters, PHB, saturated chloro-alkane and motor oil as the sole carbon source (Figure 17-Figure 19). Our second round of experiments will focus on optimizing the process of uniformly coating the medium surface with chemicals as we had uneven deposition of chemical crystals on the plates. Uneven coating can affect LMJ's utilization of aromatic chemicals.
Acidovorax sp. DP5 displays a high extracellular depolymerase enzyme activity when grown in medium containing 0.25% (w/v) of PHB and 1 gram/L of urea as carbon and nitrogen source, respectively 32 . The depolymerase enzyme produced by strain Acidovorax sp. DP5 showed high percentage of degradation of PHB films in an alkaline condition at pH 9 under a temperature of 40°C 32 . Our third round of experiments would be to test different types of nitrogen sources, pH and temperature that would allow optimal growth on PHB and PAH-containing TP medium plates. It would be interesting to compare the growth of LMJ on M9 bacterial minimal medium against the growth on TP medium, when testing alternative carbon sources, as M9 medium has a higher phosphate and nitrogen content than the TAP medium, respectively (Table 1). We need to collaborate with a research lab that can test the concentration of these chemicals on the TP medium plates before and after the LMJ growth to get additional support that LMJ is removing PHB, PAH and other hydrocarbons in the TP medium plates.
In summary, LMJ shares morphological and many biochemical traits with Acidovorax sp. Currently in the NCBI database, there are 60 genome assemblies of 17 characterized Acidovorax species and 67 genome assemblies of uncharacterized Acidovorax environmental isolates. The genome of the nearest relative of LMJ, Acidovorax sp. strain A16OP12, an environmental isolate, has not been sequenced yet. Because of funding limitations, we could not sequence the whole genome of LMJ at the time of this study. But we will have funds in fall 2020 to sequence the LMJ's genome using Pacific Biosciences technology. This will allow us to: 1) determine assign a specific scientific genus/species/strain name to LMJ and, 2) will identify the genes in LMJ that play a role in its metabolic diversity relevant to bioremediation of common environmental pollutants. This project contains the following underlying data:

Data availability
• Data S1 LMJ (XLSX). (Means and standard  This project contains 16 images of antibiotic plates used for the antibiotic susceptibility tests using the disc diffusion method for Chlamydomonas and the bacterial strain, LMJ. This project contains the following underlying data: • ABI extension files obtained from partial sequencing of the LMJ strain 16S rRNA.
• Corresponding text files of DNA sequences.