Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.07.08.737209

Response surface methodology for melanin nanoparticle production optimization from producer strain Pseudomonas stutzeri BTCZ305 with invitro anti-inflammatory and wound healing potential

Abstract

Culture conditions were optimized for the production of melanin nanoparticle by the bacterial strain Pseudomonas stutzeri BTCZ 305. Response surface methodology was employed for determining the most significant fermentation conditions using variables including, pH, temperature and L-tyrosine concentration identified through one-factor-at-a time approach. Box-behnken design consisting of 17 different combinations of all these factors were performed. Using this methodology, a quadratic regression model was built and the optimal combinations of media constituents for maximum melanin production 1192.27 g/mL were determined as temperature (32.5 {degrees}C), pH (8.5) and L-tyrosine concentration (7 g/L). Melanin productionwas obtained experimentally coincident with the predicted value and the model was proven to be adequate. The nanostructural distribution, its stability in colloidal suspension and particle size were also characterized with the help of TEM, particle size analysis and Zeta potential. The potent applicability of this molecule in anti-inflammation and wound healing was also elucidated. HighlightsO_LIMelanin nanoparticle synthesis by marine bacterial strain Pseudomonas stutzeri BTCZ 305 C_LIO_LIMedia optimization using one-factor-at-a-time method C_LIO_LIStatistical media optimization using Response surface methodology and Box-behnken design of experiment C_LIO_LINanoparticle characterization using TEM, particle size analysis and zeta potential. Its functional role in anti-inflammation and wound healing. C_LI

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Mathew, D., Bhatt, S. G.. 2026-07-08. Response surface methodology for melanin nanoparticle production optimization from producer strain Pseudomonas stutzeri BTCZ305 with invitro anti-inflammatory and wound healing potential. https://doi.org/10.64898/2026.07.08.737209

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A self-limiting dimeric TIR effector specialised for type III CRISPR-mediated immunity

Antiviral defence systems frequently utilise cyclic nucleotide second messengers. A prominent example is the type III CRISPR-Cas system, which generates cyclic oligoadenylates (cOA) on detecting viral RNA. cOA molecules can bind and activate a wide range of effectors to provide antiviral defence. In both prokaryotes and higher plants, activation of a catalytic Toll/Interleukin Receptor (TIR) domain by multimerization results in degradation of NAD+, limiting cell metabolism and thus viral replication. Here, we describe a CRISPR-associated TIR-containing effector that includes a SAVED (SMODS-associated and fused to various effector domains) domain for nucleotide sensing and a cOA-degrading ring nuclease Crn4 domain. We demonstrate that the TIR-SAVED-Ring nuclease (TSR1) effector binds cA3, resulting in activation of the TIR NADase activity. The Crn4 domain, which imposes an unusual dimeric quaternary structure on the effector, degrades cA3, providing a mechanism to auto-deactivate the effector. TSR1 is thus a highly unusual example of a dimeric and self-limiting TIR effector in antiviral immunity.

microbiology↗

DepoCat: Interactive database of experimentally verified phage depolymerases

Klebsiella phage depolymerases degrade polysaccharide capsules and exhibit narrow substrate specificity for particular capsular types. Despite a growing number of experimentally characterized enzymes, these data remain scattered throughout the scientific literature, while existing protein sequence repositories are dominated by entries with computationally assigned, unverified functional annotations. Here we present DepoCat, the first interactive database of phage depolymerases with experimentally verified function and specificity, available at http://depocat.uwr.edu.pl. The database currently contains 131 proteins meeting rigorous inclusion criteria, spanning 75 distinct capsular types. Each entry integrates experimental and computational resources. The web interface provides an integrated Classifier tool with two search modes: sequence-based search and structure-based search - enabling preliminary structural classification and inference of putative substrate specificity of newly identified depolymerases. We demonstrated the utility of both modes on a set of 17 experimentally verified non-Klebsiella phage depolymerases, for which structural analysis enabled unambiguous class assignment in almost all cases despite low or undetectable sequence similarity to the database reference dataset. DepoCat constitutes a publicly accessible resource supporting research into the structural diversity and sequence-structure-specificity relationships of phage depolymerases, while also facilitating the identification of candidates for therapeutic and diagnostic applications.

microbiology↗

A two-step model of FtsZ-ring disassembly in Bacillus subtilis

Bacillus subtilis grows and divides by binary fission, directed by medial localization of cell division protein FtsZ. Disruption of either the Min system or EzrA results in aberrant FtsZ positioning. Here we compare FtsZ dynamics in cells disrupted for either MinD or EzrA when grown in microfluidic channels. Here we show that cells lacking MinD or EzrA appear to be similarly defective in Z-ring disassembly after septation, but play different roles as simultaneous disruption results in a synergistic defect in division. Moreover, we account for a low frequency of minicell formation in the absence of EzrA, as MinD but not EzrA is necessary for removal of ZapA from polar Z-rings. Finally, overexpression of MinCD results inhibits division through pervasive Z-ring disassembly but appears to concentrate ZapA through localized sequestration. Combined, our results indicate a closer relationship between MinCD and ZapA than previously recognized and show that Z-ring disassembly can be genetically separated into discrete steps. We propose a two-step model for Z-ring disassembly that mirrors the assembly process, such that after and/or during septation, the Z-ring separately decondenses and protofilaments are disassembled to monomers for recycling.

microbiology↗