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Current Chemical Biology

Editor-in-Chief

ISSN (Print): 2212-7968
ISSN (Online): 1872-3136

General Research Article

Screening and Molecular Characterization of Cellulase Producing Actinobacteria from Litchi Orchard

Author(s): Sanju Kumari, Utkarshini Sharma, Rohit Krishna, Kanak Sinha and Santosh Kumar*

Volume 13, Issue 1, 2019

Page: [90 - 101] Pages: 12

DOI: 10.2174/2212796812666180718114432

Price: $65

Abstract

Background: Cellulolysis is of considerable economic importance in laundry detergents, textile and pulp and paper industries and in fermentation of biomass into biofuels.

Objective: The aim was to screen cellulase producing actinobacteria from the fruit orchard because of its requirement in several chemical reactions.

Methods: Strains of actinobacteria were isolated on Sabouraud’s agar medium. Similarities in cultural and biochemical characterization by growing the strains on ISP medium and dissimilarities among them perpetuated to recognise nine groups of actinobacteria. Cellulase activity was measured by the diameter of clear zone around colonies on CMC agar and the amount of reducing sugar liberated from carboxymethyl cellulose in the supernatant of the CMC broth. Further, 16S rRNA gene sequencing and molecular characterization were placed before NCBI for obtaining recognition with accession numbers.

Results: Prominent clear zones on spraying Congo Red were found around the cultures of strains of three groups SK703, SK706, SK708 on CMC agar plates. The enzyme assay for carboxymethylcellulase displayed extra cellulase activity in broth: 0.14, 0.82 and 0.66 µmol mL-1 min-1, respectively at optimum conditions of 35°C, pH 7.3 and 96 h of incubation. However, the specific cellulase activities per 1 mg of protein did not differ that way. It was 1.55, 1.71 and 1.83 μmol mL-1 min-1. The growing mycelia possessed short compact chains of 10-20 conidia on aerial branches. These morphological and biochemical characteristics, followed by their verification by Bergey’s Manual, categorically allowed the strains to be placed under actinobacteria. Further, 16S rRNA gene sequencing, molecular characterization and their evolutionary relationship through phylogenetics also confirmed the putative cellulase producing isolates of SK706 and SK708 subgroups to be the strains of Streptomyces. These strains on getting NCBI recognition were christened as Streptomyces glaucescens strain SK91L (KF527284) and Streptomyces rochei strain SK78L (KF515951), respectively.

Conclusion: Conclusive evidence on the basis of different parameters established the presence of cellulase producing actinobacteria in the litchi orchard which can convert cellulose into fermentable sugar.

Keywords: Actinobacteria, carboxymethylcellulose, cellulase, Streptomyces, 16S rRNA gene sequence, litchi orchard.

Graphical Abstract

[1]
Lynd LR, Weimer PJ, Van Zyl WH, Pretorius IS. Microbial cellulose utilization: Fundamentals and biotechnology. Microbiol Mol Biol Rev 2002; 66(3): 506-77.
[2]
Xing-hua L, Hua-jun Y, Roy B, et al. The most stirring technology in future: Cellulase enzyme and biomass utilization. J Microbiol Biotechnol 2009; 1: 229-33.
[3]
Cherry JR, Fidants AL. Directed evolution of industrial enzymes: An update. Curr Opin Biotechnol 2003; 14: 438-43.
[4]
Venkata NRE, Goli D, Rajesh T, et al. Screening and isolation of cellulase producing bacteria from dump yards of vegetable wastes. W J Phar Pharmaceu Res 2013; 3: 428-35.
[5]
Arifin H, Abdullah N, Umi K, Shirai Y, Hassan MA. Production and characterization by Bacillus pumilus EB3. Int J Eng Technol 2006; 3: 47-53.
[6]
Arunachalam R, Wesely EG, George J, Annadurai G. Novel approaches for identification of Streptomyces noboritoensis TBG-V20 with cellulase production. Curr Res Bacteriol 2010; 3: 15-26.
[7]
Li W, Zhang WW, Yang MM, Chen YL. Cloning of the thermosi cellulase gene from newly isolated Bacillus subtilis and its expression in Escherichia coli. Mol Biotechnol 2009; 40: 195-201.
[8]
Koomnok C. Selection of cellulase producing thermophilic fungi. 31st Congress on Science and Technology of Thailand of Technology. 2005 Oct 18-20; 2005.
[9]
Pathom-aree W, Stach JEM, Ward AC, et al. Diversity of actinomycetes isolated from challenger deep sediment (10,898m) from the Mariana Trench. Extremophiles 2006; 10: 181-9.
[10]
Okoro CK, Brown R, Jones A, et al. Diversity and cultivable actinomycetes in hyper-arid soils of the Atacama Desert, Chile. Antonie van Leeuwenhoek 2009; 95(2): 121-33.
[11]
Goodfellow M. Williams. ST. Ecology of actinomycetes. Annu Rev Microbiol 1983; 37: 189-216.
[12]
Goodfellow M. Selective Isolation of actinobacteria.Manual of industrial microbiology and biotechnology. Washington, DC: ASM Press 2010; pp. 13-27.
[13]
Goodfellow M, Kampfer P, Busse H-J, et al. Bergey’s manual of systematic bacteriology. New York: Springer 2012; Vol. 5.
[14]
Chakraborty N, Sarker SC, Lahiri SC. Cellulose degrading capabilites of cellulolytic bacteria isolated from the intestinal fluids of the silver cricket. Environmentalist 2000; 20(1): 9-11.
[15]
Stackebrandt E, Rainey FA, Ward-Rainey NL. Proposal for a new hierarchic classification system, Actinobacteria classis nov. Int J Syst Bacteriol 1997; 47: 479-91.
[16]
Weisburg WG, Barns SM, Pelletier DA, Lane DJ. 16S ribosomal DNA amplification for phylogenetic study. J Bacteriol 1991; 173(2): 697-703.
[17]
Williams ST, Goodfellow M, Alderson G, Wellington EMH, Sneath PHA, Sackin M. Numerical classification of Streptomyces and related genera. J Gen Microbiol 1983; 129: 1743-813.
[18]
Rodicio MR, Mendoza MC. Identification of bacteria through 16S rRNA sequencing: Principles, methods and applications in clinical microbiology. Enferm Infecc Microbiol Clin 2004; 22: 238-45.
[19]
Michael JJ, Sharon LA. 16S rRNA gene sequencing for bacterial identification in the diagnostic laboratory: Phrases, perils and pitfalls. J Clin Microbiol 2007; 45: 2761-4.
[20]
Bosshard PP, Abels S, Zbinden R, Bottger EC, Altwegg M. Ribosomal DNA sequencing for identification of aerobic gram-positive rods in the clinical laboratory (an 18-month evaluation). J Clin Microbiol 2003; 41: 4134-40.
[21]
Shirling EB, Gottlieb D. Method for the characterization of Streptomyces species. Int J Syst Bacteriol 1966; 16: 159-67.
[22]
Hankin L, Anagnostakis SL. Solid media containing carboxymethylcellulose to detect Cx cellulase activity of microorganisms. J Gen Microbiol 1977; 98: 109-15.
[23]
Apun K, Jong BC, Sellah MA. Screening and isolation of a cellulolytic and amylolytic Bacillus from sago pith waste. J Gen Appl Microbiol 2000; 46: 263-7.
[24]
Miller GL. Use of dinitrosalicyclic acid reagent for determination of sugar. Anal Chem 1959; 31: 426-8.
[25]
Nurkanto A. Cellulolitic activities of actinomycetes isolated from soil rhizospheres of Waogeo, Raja Ampat, West Papua. Jurnal Tanah Tropika 2009; 14: 239-44.
[26]
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Measurement with folin phenol reagent. J Biol Chem 1951; 193: 256-75.
[27]
Hintermann G, Crameri R, Kieser T, Hiitter R. Restriction analysis of the Streptomyces glaircescens by agarose gel electrophoresis. Arch Microbiol 1981; 130: 218-22.
[28]
Wang TY, Wang L, Zhang JH, Dong WH. A simplified universal genomic DNA extraction protocol suitable for PCR. Genet Mol Res 2011; 10: 519-25.
[29]
McGinnis S, Madden TL. Blast: At the core of a powerful and diverse set of sequence analysis tools. Nucleic Acids Res 2004; 32(Suppl. 2): W20-5.
[30]
Tamura K, Dudley J, Nei M, Kumar S. MEGA 4: Molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol 2007; 24: 1596-9.
[31]
Olmezoglu E, Herand BK, Oncel MS, Tune K, Ozkan M. Copper bioremoval by novel bacterial isolates and their identification by16S rRNA gene sequence analysis. Turk J Biol 2012; 36: 469-76.
[32]
Kumari S. Studies on PCR mediated amplification of AUD (Amplifiable Unit of DNA) in actinomycetes. Muzaffarpur, India: B R A Bihar University 2015.
[33]
Sharma U, Kumari S, Sinha K, Kumar S. Isolation and molecular characterization of phytase producing actinobacteria from fruit orchard. Nucleus 2017; 60: 187-95.
[34]
Bhat MK. Cellulases and related enzymes in biotechnology. Biotechnol Adv 2000; 18: 355-83.
[35]
Mohanta YK. Isolation of cellulase-degrading actinomycetes and evaluation of their cellulolytic potential. Bioengin Biosci 2014; 2: 1-5.
[36]
Singhania RR, Sukumaran RK, Patel AK, Larroche C, Pandey A. Advancement and comparative profiles in the production technologies using solid state and submerged fermentation for microbial cellulases. Enz Microb Tech 2010; 46: 541-9.
[37]
Immanuel G, Dhanusha P, Prema P, Palavesam A. Effect of different growth parameters on endonuclease enzyme activity by bacteria isolated from coir retting effluents of estuarine environment. Int J Environ Sci Technol 2006; 3: 25-34.
[38]
Hopwood DA. Forty years of genetics with Streptomyces: From in vivo through in vitro to in silico. Microbiol 1999; 145: 2183-202.
[39]
Kumar S, Sinha U. Delayed senescence in a thermophilic actinomycete by calcium ions in shake culture. Microb Lett 1989; 42: 55-9.
[40]
Vinogradova SP, Kushnir SN. Biosynthesis of hydrolytic enzymes during co-cultivation of macro- and micromycetes. Appl Biochem Biotechnol 2003; 39: 573-5.
[41]
Weisburg WG, Barns SM, Pelletier DA, Lane DJ. 16S ribosomal DNA amplification for phylogenetic study. J Bacteriol 1991; 173: 697-703.
[43]
Kieser T, Bibb MJ, Buttner MJ, Chater KF, Hopwood DA. Practical Streptomyces Genetics. Norwich, England: The John Innes Foundation 2000.

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