Performance analysis of Pseudomonas sp. strain SA3 in naphthalene degradation using phytotoxicity and microcosm studies.

The present study is aimed to develop a microbial system for efficient naphthalene bioremediation. A phytotoxicity study was carried out to check the naphthalene detoxification efficiency of Pseudomonas sp. strain SA3 in mung bean (Vigna radiata). For this, administration of the degraded product (supernatant) of 500 mg L-1 naphthalene by Pseudomonas sp. strain SA3 was studied on V. radiata till 168 h. The growth parameters of mung bean seedlings exposed to treated naphthalene solution were statistically similar to distilled water but a twofold decrease when exposed to untreated naphthalene solution. Further, through the soil microcosm study, the naphthalene degradation by pure colonies of Pseudomonas sp. strain SA3 was 6.8% higher as compared to when the natural microflora was mixed with Pseudomonas sp. strain SA3. Further naphthalene degradation by a microcosm model revealed that with an increased concentration of glucose, the carbon dioxide trap rate decreases.

Naphthalene degradation studies using Pseudomonas sp. strain SA3 from Alang-Sosiya ship breaking yard, Gujarat.

Polycyclic aromatic hydrocarbons (PAHs) remediation has received considerable attention due to their significant health concern and environmental pollution. However, PAHs contaminated sites also contain indigenous microbes that can potentially degrade naphthalene. Therefore, this study aimed to isolate, characterise and optimise process parameters for efficient naphthalene degradation. A total of 50 naphthalene degrading bacteria were isolated from Alang-Sosiya ship breaking yard, Bhavnagar, Gujarat and screened for their naphthalene degrading capacity. The selected isolate, Pseudomonas sp. strain SA3 was found to degrade 98.74 ± 0.00% naphthalene at a concentration of 500 ppm after 96 h. Further, optimisation of environmental parameters using one factor at a time approach using different inoculum sizes (v/v), pH, salinity, temperature, carbon and nitrogen source greatly accelerated the degradation process attaining 98.6 ± 0.46% naphthalene degradation after 72 h. The optimised parameters for maximum naphthalene degradation were pH 8, 0.1% peptone as nitrogen source, 8% salinity and 1% (v/v) inoculum size.

Ameliorating process parameters for zeaxanthin yield in Arthrobacter gandavensis MTCC 25325.

The present study aims to escalate the production of prophylactic agent zeaxanthin using a screened potential bacterial isolate. For this purpose, a freshwater bacterium capable of producing zeaxanthin was isolated from Bor Talav, Bhavnagar. The 16S rRNA sequence confirmed the isolate as Arthrobacter gandavensis. The bacterium was also submitted to Microbial Type Culture Collection, CSIR-Institute of Microbial Technology, Chandigarh, India, with the accession number MTCC 25325. The chemo-metric tools were employed to optimise the influencing factors such as pH, temperature, inoculum size, agitation speed, carbon source and harvest time on zeaxanthin yield. Thereafter, six parameters were narrowed down to three factors and were optimised using the central composite design (CCD) matrix. Maximum zeaxanthin (1.51 mg/g) was derived when A. gandavensis MTCC 25325 was grown under pH 6.0, 1.5% (w/v) glucose and 10% (v/v) inoculum size. A high regression coefficient (R2= 0.92) of the developed model indicated the accurateness of the tested parameters. To the best of our knowledge, this is the first report on tailoring the process parameters using chemo-metric optimisation for escalating the zeaxanthin production by A. gandavensis MTCC 25325.