Effects of light intensities and photoperiods on growth and proteolytic activity in purple non-sulfur marine bacterium, Afifella marina strain ME (KC205142)

Afifella marina strain ME (KC205142), a purple non-sulfur bacterium was isolated from mangrove habitats of Sabah. The effects of light intensities and photoperiods on proteolytic activity in Afifella marina strain ME (KC205142) were investigated. Secretion of proteolytic enzymes in Afifella marina was preliminarily assessed by skim milk agarose media. Subsequently, light intensities, such as, dark, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500 and 5000 lux were used to evaluate the effects on proteolytic activity in Afifella marina strain ME under anaerobic condition. After that, the effect of photoperiods on proteolytic activity was monitored under anaerobic light condition (3000 lux) at 0 h (0L/24D), 6 h (6L/18D), 12 h (12L/12D), 18 h (18L/6D) and 24 h (24L/0D) of photoperiod. The highest proteolytic activity of 74.67 U was recorded at 3000 lux illumination light intensity. The proteolytic activity in bacterium Afifella marina strain ME was positively associated with the dry cell weight. The proteolytic activity of 72.67 U in bacterium Afifella marina strain ME at 18 h (18L/6D) photoperiod is not significantly different (p > 0.05) from proteolytic activity of 74.67 U recorded at continuous light (24L/0D) condition. Light intensity of 3000 lux, culture period of 48 h and a photoperiod of 18 h (18L/ 6D) were the optimum parameters for proteolytic activity in bacterium Afifella marina strain ME.

[1]  Sandhya Mishra,et al.  Purification and characterization of haloalkaline thermoactive, solvent stable and SDS-induced protease from Bacillus sp.: a potential additive for laundry detergents. , 2012, Bioresource technology.

[2]  A. Chagas,et al.  Lipase Activity among Bacteria Isolated from Amazonian Soils , 2011, Enzyme research.

[3]  Y. Wang Use of probiotics Bacillus coagulans, Rhodopseudomonas palustris and Lactobacillus acidophilus as growth promoters in grass carp (Ctenopharyngodon idella) fingerlings , 2011 .

[4]  Surendra P. Singh,et al.  Screening, production, optimization and characterization of cyanobacterial polysaccharide , 2011 .

[5]  K. Jaeger,et al.  Extracellular enzymes affect biofilm formation of mucoid Pseudomonas aeruginosa. , 2010, Microbiology.

[6]  Ufuk Gündüz,et al.  Photosynthetic bacterial growth and productivity under continuous illumination or diurnal cycles with olive mill wastewater as feedstock , 2010 .

[7]  G. Jayaraman,et al.  Production of extracellular protease from halotolerant bacterium, Bacillus aquimaris strain VITP4 isolated from Kumta coast , 2009 .

[8]  R. Rajakumar Optimization of Protease Enzyme Production Using Bacillus Sp. Isolated from Different Wastes , 2009 .

[9]  Wang Changhai,et al.  Effects of Light Regime on Extracellular Polysaccharide Production by Porphyridium Cruentum Cultured in Flat Plate Photobioreactors , 2008, 2008 2nd International Conference on Bioinformatics and Biomedical Engineering.

[10]  J. Imhoff,et al.  Rhodobacter vinaykumarii sp. nov., a marine phototrophic alphaproteobacterium from tidal waters, and emended description of the genus Rhodobacter. , 2007, International journal of systematic and evolutionary microbiology.

[11]  S. Vikineswary,et al.  Biological Characterization of Rhodomicrobium vannielii Isolated from a Hot Spring at Gadek, Malacca, Malaysia , 2006 .

[12]  J. T. Staley,et al.  The alpha-, beta-, delta-, and epsilonproteobacteria , 2005 .

[13]  K. Oda,et al.  Purification and Characterization of Alkaline Serine Proteinase from Photosynthetic Bacterium, Rubrivivax gelatinosus KDDS1 , 2004, Bioscience, biotechnology, and biochemistry.

[14]  K. Ramachandran,et al.  Rhodovulum sulfidophilum in the treatment and utilization of sardine processing wastewater , 2004, Letters in applied microbiology.

[15]  S. Sen,et al.  Enzyme producing bacterial flora isolated from fish digestive tracts , 2002, Aquaculture International.

[16]  Richard A. Gross,et al.  The accumulation of poly(3-hydroxyalkanoates) in Rhodobacter sphaeroides , 1991, Archives of Microbiology.

[17]  B. M. Veeregowda,et al.  Biofilms: A survival strategy of bacteria , 2003 .

[18]  V. Chong,et al.  Phototrophic Bacteria as Feed Supplement for Rearing Penaeus monodon Larvae , 2002 .

[19]  R. Herrmann,et al.  Identification and Characterization of SppA, a Novel Light-inducible Chloroplast Protease Complex Associated with Thylakoid Membranes* , 2001, The Journal of Biological Chemistry.

[20]  A. Tsygankov,et al.  USE OF IMMOBILIZED PHOTOTROPHIC MICROORGANISMS FOR WASTE WATER TREATMENT AND SIMULTANEOUS PRODUCTION OF HYDROGEN , 1998 .

[21]  S. Takaichi,et al.  Porphyrobacter tepidarius sp. nov., a moderately thermophilic aerobic photosynthetic bacterium isolated from a hot spring. , 1997, International journal of systematic bacteriology.

[22]  A. Hiraishi,et al.  A new genus of marine budding phototrophic bacteria, Rhodobium gen. nov., which includes Rhodobium orientis sp. nov. and Rhodobium marinum comb. nov. , 1995, International journal of systematic bacteriology.

[23]  S. Suwanno,et al.  Optimization for growth of Rhodocyclus gelatinosus in seafood processing effluents , 1993, World journal of microbiology & biotechnology.

[24]  K. Schleifer,et al.  The Prokaryotes. A handbook on the biology of bacteria: ecophysiology, isolation, identification, applications. Volumes I-IV. , 1992 .

[25]  R. Chróst Environmental Control of the Synthesis and Activity of Aquatic Microbial Ectoenzymes , 1991 .

[26]  H. Ohigashi,et al.  Inactivation of T5 phage by cis-vaccenic acid, an antivirus substance from Rhodopseudomonas capsulata, and by unsaturated fatty acids and related alcohols. , 1991, FEMS microbiology letters.

[27]  S. Nagai,et al.  SELECTION OF RHODOBACTER SPHAEROIDES P47 AS A USEFUL SOURCE OF SINGLE CELL PROTEIN , 1986 .

[28]  U. Winkler,et al.  Glycogen, hyaluronate, and some other polysaccharides greatly enhance the formation of exolipase by Serratia marcescens , 1979, Journal of bacteriology.