Halomonas Venusta Mediated Detoxication and Biotransformation of Selenite Into Selenium Nanoparticles Exhibiting Various Biomedical Applications

Marine environment is in constant threat due to anthropogenic activities which are involved in disturbing the aquatic ora and fauna due to accumulation of toxic metals and metalloids. The current study involves the use of microbial remediation strategy for reduction of toxic sodium selenite (Na 2 SeO 3 ) into less toxic elemental Se (Se 0 ) with concurrent synthesis of Se nanoparticles (SeNPs) possessing several biomedical potential. Selenite reducing bacterial strain isolated from Mandovi estuary of Goa, India was identied as Halomonas venusta based on 16S rRNA gene sequence analysis and designated as strain GUSDM4. It's maximum tolerance level for Na 2 SeO 3 was 100 mM. The 2, 3-diaminonaphthalene based spectroscopic analysis clearly demonstrated 93% reduction of 4 mM Na 2 SeO 3 to Se 0 during late stationary growth phase of Halomonas venusta. Biosynthesis of SeNPs commenced within 4 h during log phase which was clearly evident from red colour in the growth medium and a characteristic peak at 265 nm revealed by UV-Vis spectrophotometry. The intracellular synthesis of SeNPs was conrmed by transmission electron microscopy (TEM) of these bacterial cells. Characterization of SeNPs by X-ray crystallography, TEM and energy dispersive X-ray analysis clearly demonstrated spherical SeNPs of 20-80 nm diameter with hexagonal crystal lattice. These SeNPs at 50 µg/mL exhibited 90% free radical scavenging activity and also demonstrated anti-biolm activity at 20 µg/mL against common human pathogens which was evident by SEM analysis. These SeNPs interestingly revealed excellent dose-dependent and selective anti-proliferative activity against A549 cancer cell line and mosquito larvicidal activity against Aedes aegypti, Culex quinquefasciatus and Anopheles stephensi. Therefore, these studies have demonstrated amazing potential of marine bacterium, Halomonas venusta in bioremediation along with biosynthesis of SeNPs and their applications as free radical scavenger, anti-biolm, chemotherapeutic and larvicidal agents which is the rst report of its kind. toxic selenite to elemental selenium and biosynthesis of SeNPs with value added characteristics. In the present investigation, we have reported for the rst time biosynthesis of SeNPs using estuarine bacterial strain Halomonas venusta which showed anti-oxidant, anti-cancer and mosquito larvicidal potential.


Introduction
The extensive industrialization and various anthropogenic activities have signi cantly contaminated the estuarine environment with several metalloid pollutants viz. arsenic, tellurium and selenium over past several decades disturbing its ecological balance. Environmental protection from toxic metal and metalloid pollutants released in the aquatic and terrestrial environment requires speci c strategies to protect and restore these contaminated environments. Therefore, extensive broadening of research spectrum for bioremediation of these pollutants by diverse group of microorganisms is of great concern for environmental microbiologists.  (Allan et al. 1999). It is commonly referred as 'double-edged sword' since in human beings the nutritional dose of Se (i.e. 200-400 µg/day) boosts immunity and also promotes cell death (Arthur et al. 2003; Zeng et al. 2008). Moreover, its de ciency leads to 'Keshan disease' and excess of Se (<400 µg/mL) causes selenosis (Chen 2012; Morris and Crane 2013).
Selenite is introduced into the environment mainly due to weathering of rocks, coal carbonization, seleniferous agricultural drainage, sewage and e uents from various industries viz. glass, plastic, paint, pigments, oil and tanneries (Javed et al. 2015). Selenite contamination of water bodies and apparently drinking water adversely affects human health due to its biomagni cation (Ouédraogo et al. 2015). Being Selenite bioreduction to insoluble elemental selenium by bacteria can be nanostructured since the process of bioreduction and nanoparticle synthesis takes place simultaneously (Tan et al. 2016).
Therefore, the use of estuarine bacteria for simultaneous selenite reduction and biosynthesis of nanomaterials will certainly be highly favourable, environmental friendly and economically viable. Since other chemical and physical processes involve environmentally hazardous techniques along with the use of toxic materials and radiations (Velmurugan et al. 2014;Presentato et al. 2018).
Selenium in nano-dimensions has gained tremendous attention and are high in demand due to its extensive applications in electronics, agriculture, food, feed and environmental bioremediation along with a special emphasis in the eld of medicine due to its crucial biological role even at low concentration (Shirsat et al. 2015). The speci city, selectivity, bioavailability and low toxicity of SeNPs make them one of the most promising candidate to be used for biomedical applications. The antioxidant activity of SeNPs has gained tremendous attention worldwide; on the other hand, developing an antioxidant with low cost and toxicity remains a challenging task. Thus, development of a novel nontoxic, nano-Se antioxidant is desirable and imperative.
Se is also known as anti-microbial and anti-bio lm agent against diverse microbial pathogens. Due to the increasing drug resistance worldwide, scientists are now looking out for alternative antimicrobials to treat microbial infections. The problem is severe while handling bio lm-associated microbial infections. Under such circumstance's development of a novel, antibio lm material in nano-forms is mandatory. SeNPs have also been studied widely for their anti-cancer activity against various cancer cell lines (Chen et al. 2008;Zheng et al. 2011;Luo et al. 2012). Several concerns and complications in current anti-cancer therapy including non-speci city, non-selectivity, rapid drug deactivation, reduced pharmacokinetics, restricted bio-distribution, side effects and cost-effectiveness of anti-cancer drugs have severely hampered the effectiveness of treatments. However, SeNPs address all the above concerns making them ideal and most demanding novel anti-cancer drug.
It's worth mentioning that every year 70 million people are affected due to mosquito-borne diseases globally, among which 4 million is Indian population (Ghosh et al. 2012). Mosquito acts as an important vector for most of the fatal and life-threatening vector borne diseases viz. malaria, dengue, yellow fever, lariasis, zika and chikungunya. These diseases pose a serious threat to both developing and developed countries across the globe due to their re-emergence and tendency to spread outside the known geographic regions causing epidemics. Nanoparticle-based approach to control this vector would be very promising due to its speci city. In the present study, we have reported Halomonas venusta mediated detoxi cation and biotransformation of selenite into selenium nanoparticles exhibiting anti-oxidant, antibio lm, anticancer, and mosquito larvicidal activity.

Materials And Methods
Isolation of selenite reducing estuarine bacteria

Determination of Minimum inhibitory concentration (MIC) for selenite
To determine the MIC for Na 2 Se0 3, the selected bacterial isolates were spot inoculated on ZMA plates with increasing concentrations of Na 2 Se0 3 (0-120 mM). The plates were incubated at 25 °C ± 2 for 24 h and were checked for appearance of brick red coloured colonies. The minimum concentration at which no visible colonies obtained was designated as MIC. Bacterial isolates with the highest MIC on solid media were selected for determining their MIC in the liquid medium. The strains were grown in the presence of various concentrations of sodium selenite (0-120 mM) and were checked for absorbance at 600 nm after 24 h of incubation.
Identi cation of selenite reducing bacterial strain GUSDM4 DNA extraction of the selenite reducing bacterial strain GUSDM4 was carried out using Dneasy® Blood & Tissue Kit (Qiagen, Hilden, Germany). Universal eubacterial primers: 27F (5'-AGAGTTTGATCMTGGCTCAG-3') and 1492R(5'-TACGGYTACCTTGTTACGACTT-3') were used to amplify 16S ribosomal RNA gene (16S rRNA) using Nexus Gradient Mastercycler (Eppendorf, Germany). The PCR amplicon was analysed on 1% agarose gel followed by puri cation using Wizard SVGel and PCR clean-up system (Promega, USA). The puri ed 16S rRNA gene was sequenced at Euro ns Genomics, Bangalore, India followed by BLAST analysis and the DNA sequence was submitted to Genbank (Altschul et al. 1990). The Phylogenetic dendrogram was constructed by the Neighbor-joining method using MEGA 7 software (Tamura et al. 2013).

Selenite uptake by bacterial strain GUSDM4
Time course study of selenite uptake was done using a modi ed spectrophotometric method as described by Watkinson (1996). Brie y, H. venusta GUSDM4 was grown in the presence of 2 and 4 mM Na 2 SeO 3 and every 4 h, 0.5 mL aliquot was centrifuged at 9727 X g for 10 min. The supernatant (100 µL) was used to determine the selenite content. Appropriate controls such as un-inoculated medium with Na 2 SeO 3 and inoculated medium without metal were kept and processed under similar conditions. For selenite estimation, 0.1 M HCl (5 mL), 0.1M NaF (0.25 mL) and 1M disodium oxalate (0.25 mL) were added and mixed in a test tube. Subsequently, 0.25 mL culture supernatant, 1.25 mL of 0.1% 2,3 DAN (2,3-diaminonaphthalene) was added, mixed and incubated at 60 °C for 15 min. The above mixture was cooled at room temperature and 3 mL of cyclohexane was added to extract selenium -2,3 DAN complex with vigorous shaking. The solution was then centrifuged at 3000 X g for 12 min and absorbance at 377 nm of the organic phase was determined using UV-Vis spectrophotometer (Shimadzu -1601, Japan). The experiments were performed in triplicates and the standard error was determined.

Biosynthesis and localization of SeNPs by Halomonas venusta strain GUSDM4
The bacterial strain GUSDM4 was inoculated in ZMB supplemented with 2 mM Na 2 SeO 3 , incubated at 25°C mM. The culture was inoculated in ZMB asks with varying pH, temperature and sodium selenite concentrations respectively. The nanoparticle biosynthesis was monitored at 265 nm using UV-Vis spectrophotometer which is characteristic for elemental selenium. Time course study for the biosynthesis of SeNPs was also carried out under optimized conditions. The SeNPs were obtained by the protocol described by Vaigankar et al. (2018).

Characterization of biosynthesized nanoparticles
Biosynthesized SeNPs were suspended in methanol: chloroform (2:1 v/v) and analysed for their characteristic optical properties by scanning between 190 to 800 nm using UV-Vis spectrophotometer (Shimadzu-2450, Japan). X-ray diffraction pattern for biosynthesized SeNPs was obtained using X-ray diffractometer (Rigaku Mini ex). The Scherrer's equation was used to calculate the crystal size of the nanoparticles: where D is the mean grain size, k is constant, λ is the X-ray wavelength for CuKa radiation, β is the FWHM of the diffraction peak in radians and θ is the Braggs angle. The TEM analysis of the SeNPs was carried out to determine the morphology of the nanoparticles. SeNPs powder was dispersed in methanol and mounted on a carbon-coated copper TEM grid (Philips, model-CM200). The size of the SeNPs was calculated using Image J software. Energy dispersive X-ray analysis was also carried out to determine the elemental composition of the biogenic nanoparticles. SeNPs were coated with a thin lm of carbon and analysed for energy dispersive X-ray analysis using a scanning electron microscope along with EDS (JSM 5800 LV, model-JOEL, Japan).

Applications of biogenic SeNPs
Anti-oxidant activity DPPH (1,1-diphenyl-2-picryllhydrazly) free radical scavenging activity of biogenic SeNPs was investigated using a method described by Turlo et al. (2010) with minor modi cations. In the presence of antioxidant purple DPPH changes into yellow stable compound and hydrogen donating capacity of antioxidant determines the extent of reaction (Niki 2010). Different concentrations of biogenic SeNPs were mixed with 1 mL of freshly prepared 0.2 mM DPPH. These tubes were incubated in the dark for 30 min and absorbance of the samples was recorded at 570 nm spectroscopically using ascorbic acid as a standard and methanol as blank. The % free radical scavenging activity is expressed as follows: Anti-bio lm potential of SeNPs The anti-bio lm activity of biogenic SeNPs against potential human pathogens procured from Goa Medical College, Goa, India viz. Streptococcus pyogenes, Staphylococcus aureus, Klebsiella pneumoniae and Escherichia coli was studied using modi ed crystal violet assay in a 96 well sterile polystyrene microtiter plate as described previously ). Percent antibio lm was calculated using the following formula: where Absorbance of control corresponds to the bacterial cells grown in nutrient broth without NPs. The anti-bio lm assay was carried out in triplicate and the standard deviation was determined. To further con rm this SEM analysis of the bacterial pathogens grown in the presence of (0, 20, 25 and 50µg/mL SeNPs) were carried out as per the protocol described in Mujawar et al. (2019).

Anti-cancer activity (MTT assay)
Biogenic SeNPs were evaluated for their cytotoxicity against cancer cells by MTT (3-(4, 5-dimethylthiazol-2-yl) -2, 5-diphenyltetrazolium bromide) assay. The dye is reduced by metabolically active human cells due to the action of various dehydrogenase enzymes to pink formazan dye. The adenocarcinomic human alveolar basal epithelial and normal human bronchial epithelial cell lines were used for this study. The cell lines were cultured in Dulbecco's modi ed Eagle medium with high glucose (DMEM-HG, DMEM-F12) supplemented with 10% Foetal Bovine Serum (FBS). The cells cultured in T-25 asks were trypsinized and aspirated into 5 mL centrifuge tubes. Subsequently, the cell pellet was obtained by harvesting cells at 300 X g and the cell suspension exhibiting a cell count of 2 X 10 4 was used for the assay. The 200 μL cell suspension was added to a 96 well microtitre plate and the plates were incubated in 5% CO 2 incubator at 37 o C for 24 h. The cells were incubated with different concentrations of SeNPs for 24 h, followed by addition of MTT reagent (10%) for 4 h. The media was aspirated without disturbing the formazan crystals formed. Consequently, 100 µL of DMSO was added to the plate and absorbance at 570 nm and 630 nm was measured using UV-Visible spectrophotometer. Sodium selenite and positive control with cisplatin was also evaluated for their cytotoxicity. The experiment was carried out in triplicates and cell viability relative to unexposed cells (control) was calculated as follows: Where (A test ) is absorbance of the cells treated with SeNPs and (A control ) is absorbance of the cells without SeNPs treatment.

Larvicidal activity of biogenic SeNPs
Source of mosquito immatures The larvae of Anopheles stephensi, Culex quinquefasciatus and Aedes aegypti were obtained from ICMR-National Institute of Malaria Research, Field Unit, Goa, insectary. The cyclic colonies of these mosquito species were maintained at a temperature of 27±2 °C with a relative humidity of 70 ± 5% and a photoperiod: scotoperiod of 12:12 h (light: dark). Healthy 3 rd instar larvae were used to conduct the bioassay.

Bioassay
All the three larvae of Anopheles stephensi, Culex quinquefasciatus and Aedes aegypti were used to carry out preliminary bioassay. SeNPs were dissolved in methanol and dilutions were made to attain an appropriate range of dosage. Third instar larvae (25) were transferred to autoclaved plastic containers in 250 mL of distilled water. These were exposed to various concentrations of SeNPs ranging from 10 to 100 ppm for 24 and 48 h along with methanol control without addition of NPs suspension. After 24 and 48 h post-treatment, the number of dead larvae was counted and percent mortality was calculated for each time interval. Abbott's formula was applied to calculate corrected mortality if the control mortality (%) was between 5 and 20. Probit analysis with SPSS PASW 18.0 was used to determine LC 50 , mean and standard errors. Abbott's formula for calculating corrected mortality is as follows:

Results And Discussion
Isolation of selenite reducing estuarine bacteria and it's MIC for selenite Morphologically distinct 50 discrete brick red bacterial colonies were obtained after plating the samples on ZMA with 2mM Na 2 SeO 3 which were considered for further studies (Supplementary Fig. 1). These selected bacterial isolates did not show any brick red pigmentation upon streaking on ZMA plates without Na 2 SeO 3 ( Supplementary Fig. 2). The Mandovi estuary of Goa is contaminated with various metals and metalloids including selenium due to numerous anthropogenic and industrial activities such as shipping, tourism, mining and construction. It has already been reported that various bacterial isolates from Mandovi estuary possess resistance as well as cross-resistance to iron, manganese, cobalt, copper, zinc, Identi cation of selenite reducing bacterial strain GUSDM4 The bacterial strain GUSDM4 was found to be Gram-negative, motile, rod-shaped, catalase, nitrate and oxidase positive aerobic bacteria. 16S rRNA gene sequencing and sequence comparison against GenBank database using NCBI-BLAST search, strain GUSDM4 was identi ed as Halomonas venusta (accession number: MG430411). The dendrogram analysis revealed phylogenetic relatedness with other species of Halomonas (Fig. 1).
Strain GUSDM4 was identi ed as Halomonas venusta. Interestingly, members belonging to family Halomonadaceae are characterized by high salt tolerance (5-25% NaCl) and survival at low to high temperatures (4-40 °C). These characteristics make it a remarkable candidate for selenite bioremediation in various habitats ranging from estuaries to saline lakes and oceans. There are very few reports on selenite reduction by genus Halomonas and this is the rst detailed study on selenite reduction by Halomonas venusta isolated from Mandovi estuary showing the highest level of selenite resistance.
Selenite uptake studies using bacterial strain GUSDM4 Selenite uptake by Halomonas venusta strain GUSDM4 grown in ZMB with 2 and 4mM Na 2 SeO 3 was observed during the early log phase of growth (2 h) with a steady increase during the mid-log phase. At mid log phase (26 h), a 50% reduction of selenite was observed. However, 93% and 96% utilization of selenite was achieved at the end of the stationary growth phase for 4 mM and 2 mM respectively (Fig. 2). The uptake studies also revealed signi cant ability of the strain GUSDM4 to reduce 93% of selenite to elemental selenium during the late stationary phase (58 h) of growth. It's worth mentioning that the previous study on Rhodospirillum rubrum showed selenite reduction at the commencement of the stationary phase which is non-favaourable and also contradictory to the current study (Kessi et al. 1999). Thus, further strengthening its potential to be used for various biotechnological applications including nanoparticle biosynthesis.

Biosynthesis and localization of SeNPs by Halomonas venusta strain GUSDM4
Selenite reduction to elemental Se using strain GUSDM4 was evident by the colour change in the medium from yellow to brick red in the ask with 2 mM Na 2 SeO 3. Whereas, control ask without Na 2 SeO 3 and cell free supernatant with 2 mM Na 2 SeO 3 did not show any brick red colouration thus, con rming intracellular synthesis of SeNPs ( Supplementary Fig. 3). It was found that in the presence of selenite H. Venusta strain GUSDM4 demonstrated electron dense deposits throughout the periplasm which was distinctly absent in the control cells. Moreover, intracellular spherical deposits of SeNPs were also visible within the bacterial periplasm (Fig. 3 a, b). Halomonas venusta strain GUSDM4 successfully synthesized Se nanoparticles intracellularly which was initiated within 4 h of the growth phase and was con rmed from a characteristic at 265 nm using UV-Vis spectrophotometry.
The intracellular periplasmic nanoparticle synthesis was further con rmed using TEM analysis which exclusively demonstrated biosynthesis in exposed bacterial cells.

Optimization and time course study of SeNPs biosynthesis
Optimization of SeNPs biosynthesis with respect to pH, temperature and Na 2 SeO 3 was studied during intracellular synthesis. The optimum pH, temperature and Na 2 SeO 3 for SeNPs biosynthesis were 7, 25 °C and 4 mM respectively (Fig. 4 a, b, c). Time course study of SeNPs further revealed that the biosynthesis was initiated during early log phase (i.e. 4 h) which was evident from the colour change in the media and a distinctly sharp peak at 265 nm. Biosynthesis of SeNPs was time-dependent reaching maxima at 34 h of bacterial growth (Fig. 4d).
It was interesting to note that the estuarine strain GUSDM4 could synthesize SeNPs within a broad range of temperature (i.e. 18 to 40 °C) and pH (i.e. 5 to 10). Although MTC for the strain GUSDM4 was recorded to be 100 mM the nanoparticle synthesis was not carried at such a high concentration since it is a wellknown fact that nanoparticles at high salt concentrations tend to aggregate forming particles with a larger diameter which is undesirable (Stoeva et al. 2002). Earlier studies on SeNPs biosynthesis by marine Bacillus sp. MSh-1 demonstrated that biosynthesis was initiated after 14 h of incubation (Forootanfar et al. 2014). Therefore, our strain GUSDM4 is very e cient in the biosynthesis of SeNPs.

Characterization of biosynthesized nanoparticles
The UV-Vis spectrophotometry analysis clearly revealed an absorbance peak of brick red colloidal solution at 265 nm due to surface plasmon resonance indicating the presence of SeNPs (Fig. 5a) (Fig. 5b). TEM micrographs of SeNPs revealed spherical morphology with size ranging from 20 to 80 nm (Fig. 5d). The EDAX analysis demonstrated the absorption peaks at 1.5, 11.2 and 12.5 KeV thus, further reiterating presence of elemental Se (Fig. 5c).
The characterization of SeNPs using XRD, TEM and EDAX analysis con rmed the presence of pure spherical SeNPs exhibiting hexagonal crystal lattice with a diameter in the range of 20-80 nm. Previously, Zooglea ramigera has been reported to biosynthesize spherical SeNPs with diameter ranging from 30 to 130 nm (Srivastava and Mukhopadhyay 2013). Similarly, in another study size distribution of 200-400 nm was observed using the halophilic bacteria B. selenitriducens, S. shriftii and S. barnesii (Oremland et al. 2007). Size of NPs plays a major role in determining the functions of nanoparticles, smaller the size greater are the chances of enhancing its functionality and e ciency.

Applications of biogenic SeNPs
Anti-oxidant activity Biogenic SeNPs exhibited excellent dose-dependent anti-oxidant activity. An increasing percent free radical scavenging activity with increasing concentrations of SeNPs was recorded (Fig. 6). For instance, the percent scavenging activity at 25 µg/mL of biogenic SeNPs was recorded 50% while 90% at 50 µg/mL.
The biogenic SeNPs interestingly demonstrated 90% free radical scavenging activity at 50 µg/mL. Higher antioxidant activity of SeNPs is mainly due to the presence of seleno-enzymes viz. glutathione peroxidase and thioredoxin reductase, which are known to play a pivotal role in preventing the free radicals. Previous ndings on anti-oxidant activity by biogenic SeNPs also showed a similar dosedependent trend but at higher concentrations i.e. 100 to 1000 µg/mL. In this case, the percent scavenging activity at 100 µg/mL was 80%, while at 1000 µg/mL the activity was 100% (Ramya et al. 2015).
However, the current study demonstrated approximately 90% free radical scavenging activity at 50 µg/mL SeNPs which is highly signi cant. Moreover, another study demonstrated 23.1 ± 3.4 % free radical scavenging activity at 200 µg/mL SeNPs (Forootanfar et al. 2014). Differences in the % free radical scavenging activity may be attributed to the difference in the size of biosynthesized nanoparticles with the fact that smaller particles are known to exhibit greater free radical scavenging activity as compared to larger aggregates (Torres et al. 2012).

Anti-bio lm activity
SeNPs demonstrated dose-dependent anti-bio lm activity against Gram-positive and Gram-negative bacterial pathogens (Fig. 7a). Highest anti-bio lm activity was recorded against K. pneumonia at 20 ( (Fig. 7b). SeNPs also exhibited excellent anti-bio lm activity against four potential bio lm forming bacterial strains. The highest anti-bio lm activity was observed against K. pneumoniae followed by E. coli, S. aureus and S. pyogenes. Previously, a similar % reduction of S. aureus, P. aeruginosa and P. Mirabilis bio lms were reported (Shakibaie et al. 2015). These results also corroborated with the SEM analysis demonstrating the dislodging of bacterial bio lms. This opens a new arena of applications for SeNPs as coating agents in medical and health-related devices in order to prevent bacterial infections caused by bio lm forming bacteria. Likewise, these SeNPs may also have promising applications in industrial sectors as potential tools to combat biofouling. In addition, they can also serve as excellent candidates to eradicate bio lm formation in sewage tanks and other sewerage systems.
Anti-cancer activity Dose-dependent toxicity of SeNPs towards cancer cells was very much evident. SeNPs were very effective in inhibiting the A549 cell lines at concentrations as low as 10 µg/mL while at 70 µg/mL complete mortality was observed (Fig. 8a). Interestingly, SeNPs were ineffective against normal human bronchial epithelial cells (BEAS-2B) as no mortality was observed. We have also clearly observed effect of SeNPs on cancer cell line using electron microscopy (Fig. 8 b, c, d (Supplementary Fig. 4).
The vector control strategies mainly target adults or larvae and largely involve the use of chemical insecticides. The repetitive use of these hazardous insecticides foster various complications which mainly include development of insecticide-resistance, natural biological control system disruption, outburst of other insects and undesired effect on non-target insect spp. (Yang et al. 2002). The advantages associated with larval control include low mortalities and effective coverage due to behavioural responses of immature mosquito. Nanoparticle-based approach can be most desired due to its speci city and effectiveness at low concentrations. Thus, the use of biogenic SeNPs as a mosquito larvicidal agent would be much favourable. SeNPs synthesis within 4 h of the growth phase and was con rmed from a characteristic peak at 265 nm using UV-Vis spectrophotometry. XRD, TEM, and EDAX analysis further con rmed the presence of pure spherical SeNPs exhibiting hexagonal crystal lattice with a diameter in the range of 20-80 nm. The biogenic SeNPs interestingly demonstrated 90% free radical scavenging activity at 50µg/mL and also exhibited excellent dose dependent anti-cell proliferative characteristics. Additionally these SeNPs also revealed the larvicidal potential against mosquito spp. Thus, a biotechnologically potent estuarine Halomonas venusta strain GUSDM4 can be utilized simultaneously for bioremediation of toxic selenite to elemental selenium and biosynthesis of SeNPs with value added characteristics. In the present investigation, we have reported for the rst time biosynthesis of SeNPs using estuarine bacterial strain Halomonas venusta which showed anti-oxidant, anti-cancer and mosquito larvicidal potential.  Growth pattern and selenite uptake by strain GUSDM4 in the presence of 2 mM and 4 mM Na2SeO3.    Free radical scavenging activity of biogenic SeNPs. Ascorbic acid (Aa) served as a standard.