Evaluation of antimicrobial activities of microalgae Scenedesmus dimorphus extracts against bacterial strains

Evaluation of antimicrobial activities of microalgae Scenedesmus dimorphus extracts against bacterial strains

Habibi Z.¹, Imanpour Namin J.²*, Ramezanpour Z.²

1. Department of Fisheries, Faculty of Natural Resources, University of Guilan, Sowmehsara, Iran.

2. International Research Institute of Sturgeons, Rasht, Iran.

^*Corresponding Author’s email: javid.iman@gmail.com

(Received: June 07. 2017 Accepted: Nov. 20. 2017)

The study was conducted to analyze the existence of bioactive phytochemicals extracts in green alga Scenedesmus dimorphus and their antimicrobial role. Various solvents such as methanol, ethanol, N-hegzane and diethylether were used for extraction. The extracts of of Scenedesmus dimorphus were tested against two Gram - positive bacteria (Bacillus subtilis and Micrococcus luteus), a Gram - negative bacterium (A. hydrophila) and Escherichia coli by the agar well diffusion method. Four different methanolic, ethanolic, hexane and diethylether extracts showed effective inhibition against different bacterial pathogens. Diethylether extract was very effective against bacterial strains compared to other extracts. Methanolic extract effectively inhibited A. hydrophila in comparison with other extracts, while ethanolic extract did not have any inhibitory effect on the bacterium. Methanolic, ethanolic, hexane and diethylether extracts were analyzed by GC mass. The most abundant compounds in methanolic extract of S. dimorphus included esters, plasticizer compound and terpens, while in the ethanolic, N-hexane and diethylether extracts, the most abundant compounds were found to be plasticizers, hydrocarbon and esters. These results indicate the presence of promising antimicrobial compounds in the examined algal species. Further phytochemical studies are required to elucidate the structutre and detailed activities of these compounds. So, we achieved antimicrobial activity in the methanolic, ethanolic, hexane and ether extracts of green microalgae against some pathogenic bacteria as well as employing GC mass autogram for S. dimorphus extracts for preliminary detection of active constituents.

INTRODUCTION

Microalgae has become a very popular source of antibacterial agents and offer numerous advantages for antimicrobial studies due to their huge biodiversity and fast growth rate (Pulz & Gross 2004). Microalgae are new source of structurally - novel and biologically - active compounds in the pharmaceutical industry (Patra et al. 1944; Ely et al. 2004 and Tuney et al. 2006). Some algae produce anti-oxidative, anti-inflammatory and anti-cancer compounds (Justo et al. 2001). The cell extracts and active constituents of different algae have been shown to uphold antibacterial activity against Gram-positive and Gram-negative bacteria (Borowitzka et al. 1992). Algal biomass and compounds have an extensive range of potential applications from animal feed in aquaculture to human nutrition and health products (Borowitzka 1988; Soltani et al. 2005; Skulberg 2006). Bacterial resistance to antibiotics has become a major problem in health care and has become even more problematic to treat newly-evolving pathogenic bacteria (Sieradzki et al. 1999). Numerous studies suggest that algae can produce hundreds to thousands of diverse chemical compounds with different biological activities. These substances can inhibit the growth of microorganisms or eradicate them. There is a continuous need to discover new antimicrobial compounds with chemical structures and novel mechanism of action because of the development of resistance to the antibiotics (Bhagavathy et al. 2011). Among the major bioactive constituents of algae with demonstrated antimicrobial potential, proteins, polysaccharides, polyunsaturated fatty acids (PUFAs), especially EPA and DHA, amino acids, and antioxidants (polyphenols, flavonoids, and carotenoids) are the most important ones (Senthilkumar & Sudha 2012; Al-Saif et al. 2014). Aquatic microorganisms and algae produce a pool of underinvestigated secondary metabolites and are potential sources of drug-like compounds to inhibit pathogens (Dussault 2016). Several recent studies have been revealed that seaweed and algae are potential sources that can be used as antimicrobial products (Rabia et al. 2013; Al-Saif et al. 2014; Maftuch 2016). Large number of literature have been released about compounds derived from algae with antibacterial activity, such as acrylic acid, halogenated aliphatic compounds, terpenes (Ming 2017). However, the identification of compounds directly responsible for the antimicrobial potential of algae is still a relatively incipient field of research, mainly owing to the new kinds of compounds found in recent years (Amaro et al. 2011, Pina- Perez 2017). In this study, we investigated the antibacterial activity of methanolic, hexane, diethylether, and ethanolic extracts of S. dimorphus along with their antibacterial compounds that were extracted using specific eluent. The bacterial species challenged, belong to a type of pathogenic bacteria that easily invade the freshwater and brackish water fish. So by testing in vitro results of an extract of S. dimorphus, we get pertinent information about power of its extract against freshwater and brackish water bacteria.

MATERIALS AND METHODS

Culturing and Growth of Algal organisms

Green unicellular alga Scenedesmus dimorphus is a typical freshwater species belonging to class Chlorophyceae and order Chlorococcales. The species was isolated from a earthen freshwater pond and maintained and cultured in the laboratory under appropriate culture conditions. The Zehnder medium was used throughout the maintenance and experimental period (Kotai 1972; Schlosser 1994). A 1000 ml - conical flasks containing 5 ml growth medium were inoculated with known number of cells (5×10⁴ cell.mL^-1) at 30°C temperature on shelves illuminated by fluorescent tubes (light intensity of 2500 lux). No aeration was provided. The cultures were hand shaken every day to prevent algal cells settle down. The algae were cultured for 10 days and harvested.

Extraction of bioactive metabolites

The dried biomass was sonicated with liquid nitrogen and then was extracted with 96% methanol and 95% ethanol (Cowan 1999 and Zheng et al. 2011). Extracts were centrifuged at 100rpm for 10 min and further concentrated in vacuum under reduced pressure. The stock solutions of extract were prepared in DMSO at 50 mg.ml^-1 for evaluation of antimicrobial activity (Hussain et al. 2011 and Jelodarian et al. 2013).

Preparation of antimicrobial agents

Methanolic, ethanolic, hexane and diethyl ether extracts were tested against a panel of microorganisms including gram-ve, Aeromonas hydrophila and Escherichia coli and gram +ve B. subtilis and Micrococcus luteus‏. Stock cultures were maintained on  tryptic soy broth and nutrient agar medium at 40°C, then sub-cultured in nutrient broth at 37°C prior to antimicrobial test. Ethanolic, methanolic, N-hexane and diethylether extracts were dissolved in 5ml  DMSO,  impregnated with 50μl of algal extracts and introduced to the upper layer of the seeded agar plate. The plates were incubated overnight at 37°C. Negative controls were prepared by using DMSO. Penicillin was used as positive reference standard. After incubation, the clear zone around the discs were measured and expressed in mm as a measure of inhibitory effects.

GC/MS Analysis of Scenedesmus dimorphus crude extract

Methanolic, ethanolic, N-hexane and diethyl ether extracts of S. dimorphus were analyzed by GC/MS. The GC/MS analyses were performed by a Thermo Scientific, Trace GC Ultra / ISQ Single Quadrupole MS, HP-5MS fused silica capillary column (15 m, 0.251mm, 0.1 mm film thickness). An electron ionization system with ionization energy of 118 eV was used for GC/MS detection. Helium gas was used as carrier at a constant flow rate of 3 mL.min^-1. The temperature increased from 50°C to 120°C. The injector and MS transfer line temperature were set at 300 °C. Quantification of all identified components was examined using a percent relative peak area. Tentative identification of the compounds was performed based on the comparison of their relative retention time and mass spectra with those of the NIST, WILLY library data of the GC/MS system.

RESULTS

Methanolic extracts of S. dimorphus were tested against Gram - positive bacteria including B. subtilis, M. luteus as well as Gram - negative species such as  A. hydrophila and E. coli.

The extract of S. dimorphus effectively inhibited B. subtilis, M. luteus, A. hydrophila and E. coli with inhibition zones of 13, 13.3, 21.3 and 11 mm respectively.Ethanolic extracts of S. dimorphus inhibited the growth of M. luteus,  E. coli and B. subtilis with inhibition zones of 15.66, 13.66 and 11.66 mm. However, there was no effective inhibition or control on A. hydrophila.

N- hexane extracts of S. dimorphus inhibited the growth of M. luteus and B. subtilis with inhibition zones of 13 and 12.66 mm respectively.

It also inhibited the growth of A. hydrophila and E. coli only with smaller inhibition zone about 11.33 and 7 mm respectively. Diethylether extract of S. dimorphus inhibited the growth of M. luteus, B. subtilis,  A. hydrophila and  E. coli with inhibition zones of 23.6 , 18, 21.6 and 22.66 mm respectively.

The diethylether extract of S. dimorphus effectively inhibited the growth of M. luteus with an inhibition zone of 23.6 mm.

Since bacterial fish diseases like saddleback disease, erythrodermatitis, red spot disease, fin rot, furunculosis and vibriosis are caused by Gram-negative bacteria, the results showed that these eukaryotic algae produce active secondary metabolites which can inhibit proliferation of fish pathogens.

GC mass Analysis of S. dimorphus methanolic crude extract

The chemical composition of ethanolic, methanolic, N-hexane and diethylether extracts of S. dimorphus determined by GC mass are shown in Fig. 1. The spectrum analysis revealed the presence of 4 distinct peaks. Noteworthy, among all the examined organisms, Gram - positive  B. subtilis and Gram - negativeA. hydrophila displayed maximum susceptibility to metabolic extract ofS. dimorphus. The results of GC mass analyses confirmed that all extracts of S. dimorphus had moderate inhibitory effects against the examined microorganisms.

Table 1. Antibacterial activities of ethanolic, methanolic, N-hexane and diethylether extracts of S. dimorphus against Gram - positive and Gram - negative bacteria presented by inhibition zone diameter (mm).

Table 2. GC/MC mass analysis of ethanolic crude extract of S. dimorphus.

Fig. 1. Gas chromatographic profile of the major constituents in ethanolic extract of S. dimorphus.

Table 3. GC mass analysis of methanol crude extract of S. dimorphus.

Fig. 2. Gas chromatographic profile of the major constituents in methanolic extractof S. dimorphus.

Table 4. GC mass analysis of hexane crude extract of S. dimorphus.

Table 5. GC mass analysis of diethylether crude extract of S. dimorphus.

Fig. 3. Gas chromatographic profile of the major constituents in S. dimorphus N-hexane extract.

Fig. 4. Gas chromatographic profile of the major constituents in diethylether extractof S. dimorphus.