EXPLORATION OF ACTINOMYCETES DIVERSITY IN DIVERSE SOILS OF SOLAPUR–RAICHUR REGION AND OPTIMIZATION OF CULTURE CONDITIONS FOR MICROBIAL TRANSFORMATION OF COMPACTIN INTO PRAVASTATIN

Authors

  • Sidhant Kawade Author
  • L. H. Kamble Author

DOI:

https://doi.org/10.4238/w7tj0e41

Keywords:

Actinomycetes; soil diversity; selective isolation; pretreatment; compactin; pravastatin; bioconversion; fermentation optimization

Abstract

Actinomycetes remain one of the most prolific sources of clinically and industrially important secondary metabolites, yet their diversity in many Indian agro-industrial soils is still incompletely documented. In this study, soil samples were collected from 14 distinct habitats across the Solapur–Raichur belt of Maharashtra and Karnataka, India — including industrial, agricultural, riverine and compost-associated sites — and screened for actinomycete diversity using a combination of selective isolation media, antibiotic supplementation, and physical/chemical pretreatment strategies. Yeast extract–malt extract–dextrose agar supplemented with cycloheximide (25 µg/mL), fluconazole (50 µg/mL), nystatin (25 µg/mL) and rifampicin (50 µg/mL) gave contamination-free recovery and was selected for the study. Among pretreatments, a combination of dry heat (40 °C), 0.5% calcium carbonate and 0.5% phenol yielded the highest isolate recovery. A total of 308 morphologically distinct actinomycete isolates were recovered, dominated by white, grey, black and creamish aerial-mycelium morphotypes, with black and brown soils yielding the greatest isolate density. All 308 isolates were screened by thin-layer chromatography for their ability to bioconvert compactin to pravastatin via whole-cell hydroxylation; isolates G4 and G7 (from Sangvi village soil, Akkalkot) showed the strongest reaction intensity. Fermentation parameters were subsequently optimized for these two isolates: starch–casein–dextrose broth (SCDM), pH 7.0 7.5 and 28 °C gave the best bioconversion activity. These findings identify G4 and G7 as promising candidates for further scale-up, enzyme characterization and molecular identification as industrial biocatalysts for pravastatin production.

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Published

2026-09-23

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Section

Articles