ABSTRACT
Management of crustacean shell waste (SW) through an eco-friendly technique is an environmental obligation to control pollution. The present study showed a novel approach through the simultaneous application of proteolytic and chitinolytic bacteria to effectively degrade unprocessed crustacean SW. For this, the bacteria with concurrent chitinolytic and proteolytic activity (Bacillus subtilis, Priestia megaterium, or Bacillus amyloliquefaciens) were applied either alone or in combination with one proteolytic strain (Paenibacillus alvei) in the unprocessed lobster, crab, and shrimp SW. The method degraded the shells with high deproteinization (> 90%) and demineralization efficiency (> 90%). The degradation was confirmed through scanning electron microscopy. The highest weight loss achieved with shrimp, crab, and lobster shells was 93.67%, 82.60%, and 83.33%, respectively. B. amyloliquefaciens + P. alvei combination produced the highest weight loss in crab and lobster SW, whereas all combinations produced statistically similar weight loss in shrimp SW. There was a concurrent production of N-acetyl glucosamine (up to 532.89, 627.87, and 498.95 mg/g of shrimp, lobster, and crab shell, respectively, with P. megaterium + P. alvei and B. amyloliquefaciens + P. alvei in all SW) and amino acids (4553.8, 648.89, 957.27 µg/g of shrimp, lobster, and crab shells, respectively with B. subtilis + P. alvei in shrimp and B. amyloliquefaciens + P. alvei in crab and lobster). Therefore, it is concluded that, for the first time, efficient degradation of crustacean shell waste was observed using chitinolytic and proteolytic bacterial fermentation with the obtention of byproducts, providing a basis for further application in SW management.
ABSTRACT
PURPOSE: Myxobolus planilizae n. sp. is described from the intestinal muscles of the largescale mullet Planiliza macrolepis from Cochin backwaters, Kerala, India. METHODS: Host fishes inhabiting Cochin backwaters were collected using Chinese nets/gill nets. The morphometry and morphological studies were carried out using Nomarski differential interference contrast (DIC) optics, followed by molecular and phylogenetic analyses of the small subunit ribosomal DNA gene (SSU rDNA). RESULTS: Plasmodia small, pale white, and infect the muscles of the intestine; measured 0.13-0.22 (0.17) × 0.09-0.14 (0.13) mm. Mature myxospores pyriform in valvular view, and biconvex in sutural and apical views with a short anterior extension, and measured 7.45-8.75 (8.40) × 6.04-6.86 (6.25) µm. Shell valves with sutural ornamentations. Polar capsules two, equal, pyriform, measured 3.96-4.54 (4.45) × 2.22-2.94 (2.52) µm. Polar filament arranged in five coils, measured 24.41-34.44 (28.52) µm when extruded. In morphological and morphometric analysis, the present species exhibit remarkable variations from other species of the genus Myxobolus. In molecular analysis, the present species revealed the highest identity of 91.85% and divergence of 9.95% with related species, underlining its molecular uniqueness. In phylogenetic analysis, species of Myxobolus infecting mullets appeared as a separate clade and the present species was positioned distinctly with a high bootstrap value. CONCLUSIONS: Based on morphology, morphometry, and molecular and phylogenetic analyses, along with tissue/host specificities and geographic location, the present parasite is treated as new and is reported here as M. planilizae n. sp.
