Biosynthesis of Hygromycin-B Antibiotic by Streptomyces crystallinus AZ151 Isolated from Assuit, Egypt
2012, 2(3), 46-65.
Hygromycin B is an aminoglycoside antibiotic that kills bacteria, fungi and higher eukaryotic cells by inhibiting protein synthesis. It is biosynthesized in this research by Streptomyces sp. AZ151, isolated from soil sample in Assuit governorate and chosen among 194 actinomycete isolates. Morphological, physiological and biochemical culture characteristics as well as 16S rRNA nucleotide analysis confirmed strain AZ151 as Streptomyces crystallinus. An optimum environmental and nutritional condition in culture medium of this strain showed strong antibacterial and antifungal activities. Using organic solvent extraction, silica gel column chromatography and TLC, a high active metabolite, Hygromycin-B, was separated and identified as a suggested empirical formula of C15H30N2O10 and confirmed a biological efficiency.
and Prabakarana, 2011). The bacterial genus Streptomyces is a high
G+C content, Gram-positive filamentous soil bacteria with a complex life cycle
that includes morphological differentiation and spore formation (Del-Sol
et al., 2007). Medical geography is the influence of environmental
(natural and human) factors on biological system of human, plant and animals
which is even recognized as an effective and basic factor in mortality (Esmaeili
and Moshiri, 2011). Also, it has long been appreciated as a rich source
for the production of various secondary metabolites including many pharmaceutically
valuable compounds such as antibiotics, anti-cancer agents, immunosuppressants
and enzyme inhibitors (Hindra and Elliot, 2010; Myles,
2003). Based on 16S rDNA sequence and phylogenetic tree analysis, Khucharoenphaisan
et al. (2012) assigned Streptomyces strain FSPNRU 102 and
reported that this a new isolate belong to the Streptomyces niveoruber.
It is well documented that the biosynthesis of Streptomyces secondary
metabolites is typically regulated via multiple regulatory pathways operating
with several layers of complicated control systems (Chen
et al., 2010; Lee et al., 2005). The
rRNA sequences is a particularly powerful tool in streptomycete taxonomy. In
addition, rRNA sequence has also been useful for answering questions concerning
the horizontal transfer of genes within the genus Streptomyces (Huddleston
et al., 1997).
The crude antibiotic was tested by using pre coated Thin-Layer Chromatography
(TLC) plates and purified by column chromatography using silica gel (Augustine
et al., 2005). The antibacterial activity of Hygromycin A (HA) arises
from protein synthesis inhibition and is dependent upon a methylenedioxy bridged-aminocyclitol
moiety. Selective gene deletions and chemical complementation in Streptomyces
hygroscopicus NRRL 2388 showed that the hyg18 and hyg25 gene products, proposed
to generate a myo-inositol intermediate, are dispensable for HA biosynthesis
but contribute to antibiotic yields (Palaniappan et al.,
2009). Antibacterial compound was purified from the filtrate by solvent
extraction method. A comparative study on the total antibiotic sensitivity of
the free cells and immobilized cells showed that the immobilized strains were
found to be effective against the tested microorganisms. The immobilized cell
of actinomycetes was found to be more efficient for the production of secondary
metabolites with batch fermentation (Dhananjeyan et al.,
2010). The morphological character showed the variety of aerial hyphae and
spore forming in each strain. The dendrogram was constructed based on biodegradation
activity of tested strains (Khucharoenphaisan et al.,
This research has first confirmed the isolation Streptomyces strain, AZ151 out of 194 isolates from 44 soil samples at upper Egypt (Assuit governorate). Then it confirmed the identity of this strain, by morphological, physiological and biochemical characteristics as well as 16S rRNA, as Streptomyces crystallinus. Optimum environmental and nutritional requirements were carried out to obtain the highest yield of antibiotic. An antimicrobial compound was separated and purified from the culture broth of this strain through organic solvent extraction, column chromatography and TLC purification. It possesses strong inhibitory activity toward fungal and bacterial strains tested which give a chance to be applied in medical and other fields.
MATERIALS AND METHODS
Microorganism: The actinomycete AZ151 was isolated from soil sample
collected from Assuit governorate. It was purified using the soil dilution plate
technique described by Williams and Davies (1965).
Screening for antimicrobial activity: The anti-microbial activity was
determined according to Kavanagh (1972).
Taxonomic studies of actinomycete isolate (AZ151)
Morphological characteristics: Morphological characteristics of aerial hyphae,
spore mass, spore surface, color of aerial and substrate mycelia and soluble
pigments production were conducted by growing the organism on starch-nitrate
agar medium and Yeast extract-malt extract agar medium (Atta
et al., 2011).
Physiological and biochemical characteristics: Lecithinase was detected
using egg B yolk medium according to the method of Nitsch
and Kutzner (1969), Lipase (Elwan et al., 1977),
Protease (Chapman, 1952), Pectinase (Hankin
et al., 1971), α-amylase (Ammar et al.,
1998) and Catalase Test (Jones, 1949). Melanin pigment
(Pridham et al., 1956). Esculin broth and xanthine
have been done according to Gordon et al. (1974).
Nitrate reduction was performed according to the method of Gordon
(1966). Hydrogen sulphide production was carried out according to Cowan
and Steel (1974). The utilization of different carbon and nitrogen sources
was carried out according to Pridham and Gottlieb (1948).
Determination of Diaminopimelic acid (DAP) and sugar pattern was carried out
according to Becker et al. (1964) and Lechevalier
and Lechevalier (1970).
Color characteristics: The ISCC-NBS Color Name Charts illustrated with
centroid detection of the aerial, substrate mycelia and soluble pigments (Kenneth
and Deane, 1955).
DNA isolation and manipulation: The locally isolated actinomycete strain
was grown for 6 days on a starch agar slant at 30°C. Two milliliters of
a spore suspension were inoculated into the starch- nitrate broth and incubated
for 4 days on a shaker incubator at 200 rpm and 30°C to form a pellet of
vegetative cells (pre-sporulation). The preparation of total genomic DNA was
conducted as described by Sambrook et al. (1989).
Amplification and sequencing of the 16S rRNA gene: PCR amplification
of the 16S rRNA gene of the local actinomycete strain was conducted using two
primers, StrepF; 5.-ACGTGTGCAG CCCAAGACA-3. and Strep R; 5.ACAAGCCCTGGAAACGGGGT-3.
(Edwards et al., 1989). The PCR mixture consisted
of 30 pmol of each primer, 100 ng of chromosomal DNA, 200 μM dNTPs and
2.5 units of Taq polymerase, in 50 μL of polymerase buffer. Amplification
was conducted for 30 cycles of 1 min at 94°C, 1 min of annealing at 53°C
and 2 min of extension at 72°C. The PCR reaction mixture was then analyzed
via agarose gel electrophoresis and the remaining mixture was purified using
QIA quick PCR purification reagents (Qiagen, USA). The 16 S rRNA gene was sequenced
on both strands via the dideoxy chain termination method (Sanger
et al., 1977).
Sequence similarities and phylogenetic analysis: The BLAST program (www.ncbi.nlm.nih.gov/blast)
was employed in order to assess the degree of DNA similarity. Multiple sequence
alignment and molecular phylogeny were evaluated using BioEdit software (Hall,
Parameters controlling antimicrobial agent biosynthesis: These included; incubation period and temperature; agitation and aeration; pH values; carbon source and nitrogen sources; vitamins, MgSO4.7H2O and K2HPO4 concentrations; inoculum age and size, amino acids; and medium kinds. All these parameters have been determined by the standard methods.
Fermentation and purification of antibacterial agent
Streptomyces crystallinus, AZ151 inoculum was introduced aseptically
into each sterile flask containing the following ingredients (g L-1):
Arabinose, 20; NaNO3, 2.0; K2HPO4, 0.8; MgSO4.7H2O,
0.7; vitamin H, ppm and KCl, 0.5. The pH was adjusted at 8.0 before sterilization.
After 10 days of incubation at 35°C filtration was carried out through filter
paper Whatman No. 1 and followed by centrifugation at 5000 rpm for 15 min. Only
clear filtrates were tested for their antimicrobial activities.
Extraction: The clear filtrate was adjusted at different pH values (4-9) and extraction process was carried out using different solvents separately at the level of 1:1 (v/v). The organic phase was concentrated to dryness under vacuum using a rotary evaporator.
Precipitation: The precipitation process of the crude compound was carried out using petroleum ether (b.p. 60-80°C) followed by centrifugation at 5000 r.p.m for 15 min. The precipitate was tested for its antimicrobial activities.
Separation: Separation of the antimicrobial compound into its individual components was conducted by thin layer chromatography using chloroform and methanol (24:1, v/v) as a solvent system.
Purification: The purification of the antimicrobial compound was carried out using silica gel column (2.5x50) chromatography. Chloroform and Methanol 8:2 (v/v), was used as an eluting solvent. The column was left overnight until the silica gel (Prolabo) was completely settled. One milliliter crude extract to be fractionated was added on the silica gel column surface and the extract was adsorbed on top of silica gel. Fifty fractions were collected (each of 5 mL) and tested for their antibacterial activities.
Physico-chemical properties of antimicrobial agent
The elemental analysis of C, H, O, N and S was carried out at the microanalytical
center, Cairo University, Egypt.
Spectroscopic analysis: The IR, UV and Mass spectrum were determined at the micro analytical center of Cairo University, Egypt.
Biological activity: The Minimum Inhibitory Concentration (MIC) has
been determined by the cup method assay (Kavanagh, 1972).
Characterization of the antibacterial agent: The antibiotic produced
by Streptomyces crystallinus, AZ151 was identified according to the recommended
international references of Umezawa (1977) and Berdy
Isolation, purification and bioactivity of actinomycete isolates: Isolation and purification of actinomycete colonies (the broadest source of antibiotics) from 40 soil samples collected from various Egyptian localities e.g. (Assiut, Luxor and El-Minia governorates). The highest number of isolates (84) out of 194 (43.2%) were isolated on starch nitrate agar medium followed by 55 isolates (28.3%) on both starch casein agar and glycerol asparagine agar (data not shown). Screening test for 194 actinomycete isolates, against certain bacteria, fungi and yeast, confirmed that the highest percentage (38%) 74 active isolates was obtained against Staphylococcus aureus 90.5% (67) followed by Aternaria alternata, 43.2% (32) and Klebsiella pneumoniae, 41.8% (31) while the lowest percentage was obtained against Fusarium verticillioides 21.6% (16 isolates), Salmonella typhi 20.2% (15 isolates), Escherichia coli 9.4% (7 isolates), Aspergillus fumigatus 9.4% (7 isolates), Saccharomyces cerevisiae 8.1% (6 isolates) and Aspergillus flavus 6.7% (5 isolates) (data not shown).
Characterizations of the actinomycete isolate, AZ151
Morphological characteristics: Spore chains are spiral and rectiflexibiles,
spore masses are medium red and reddish gray, spore surfaces are smooth and
reverse color light yellow to light brown while, diffusible pigment production
is moderate yellowish brown to deep brown (Plate 1).
Cell wall hydrolysate: The cell wall hydrolysate contains LL-diaminopimelic
acid (LL-DAP) and sugar pattern not detected.
||Scanning electron micrograph of the actinomycete isolate AZ-A151
growing on starch nitrate agar medium showing spiral spore were, rectiflexibiles
and had a smooth surface. Neither sclerotic granules, sporangia nor flagellated
spores were observed (X20, 000)
Physiological and biochemical characteristics: The actinomycete isolate AZ151 could hydrolyze starch and protein, whereas lipid, pectin and catalase are negative, Melanin pigment is positive, degradation of xanthin, esculin, production of H2S, decomposition of urea, utilization of citrate and KCN are positive but nitrate reduction is negative.
The isolate under study utilizes; D-mannose, D-glucose, D-galactose, mannitol, meso-inositol, raffinose and trehalose but do not utilize, D- xylose, sucrose, L-rhamnose, L-arabinose, lactose, maltose and ribose; whereas, doubtful result was obtained with D-fructose. Good growth on L-glycine, L-asparagine and L-lysine. No growth on L-valine, L-leucine L-histidine, L-phenyl alanine and L-methionine. Moreover, no growth in the presence of up to 5% NaCl. The growth is not inhibited in the presence of 0.1% (w/v) phenol and at 451°C but inhibited in the presence of 0.01% (w/v) sodium azide. The actinomycete isolate is resistant to Ampicillin (25 μg mL-1), Nalidixic acid (30 μg mL-1), Cefoperazone (75 μg mL-1) and Fusidic acid (10 μg mL-1), whereas not resistant to Polymyxin (30 μg mL-1), Gentamicin (10 μg mL-1) and Kanamycin (30 μg mL-1) (Table 1).
Color and culture characteristics: Data recorded on AZ151 declared that, the growth of this strain was disappeared in ISP-1, moderate in ISP-2, 4, 5, 6 and 7 and good growth on SNA and ISP-3. While, the aerial mycelium appeared red on all media used except SNA medium, it was reddish gray. Substrate mycelium light brown on all media used except ISP-5 has shown light yellow. Almost all media used didn't induce any diffusible pigments except SNA shown moderate yellowed brown and ISP-6, 7 showed deep brown pigments (data not shown).
Molecular phylogeny of the selected isolate: The nucleotide sequence of the 16S rRNA gene (1.5 kb) of the actinomycete isolates AZ151 and the phylogenetic tree (as displayed by the Tree View program) revealed 92% similarity with Streptomyces crystallinus (Fig. 2). Multiple sequence alignment was conducted the sequences of the 16S rDNA gene of Streptomyces crystallinus and the sequencing product was determined as 1141 bp (Fig. 1).
|| The morphological, physiological and biochemical characteristics
of the actinomycete isolate AZ151
|-: Negative and +: Positive. ±: doubtful results, ++:
Moderate growth, +++: Good growth
Identification of actinomycete isolate, AZ151: This was performed basically
according to the recommended international Keys viz. (Buchanan
and Gibbons, 1974; Williams, 1989) and Numerical taxonomy
of Streptomyces species program (PIB WIN). On the basis of above collected
data and in view of the comparative study of the recorded properties of AZ151
in relation to the most closest reference strain, viz., Streptomyces crystallinus,
it could be concluded that it is identical on the basis of spore mass is medium
red or reddish gray, spore chain is spiral and rectiflexibiles and non motile
|| A comparative study of the characteristic properties of AZ151
in relation to reference strain, Streptomyces crystallinus
|ND: Melanin pigment not-detected
||The sequence alignment was conducted the sequences of the
16S rDNA gene of Streptomyces crystallinus
Cell wall hydrolysate contains LL-diaminopimelic acid and sugar pattern not
detected. Melanin pigments are produced. Utilization of D-mannose, D-glucose,
D-galactose, mannitol, meso-inositol, raffinose and trehalose but do not utilize
D-xylose, sucrose, rhamnose, L-arabinose, lactose, maltose and Ribose, whereas,
doubtful with D-fructose. In view of all the previous characteristics of AZ151,
it could be stated that it is suggestive of being belonging to Streptomyces
crystallinus (Table 2).
||The phylogenetic position of the local Streptomyces sp.
strain among neighboring species. The phylogenetic tree was based on the
pairwise comparisons of 16S rDNA sequences
Parameters controlling antimicrobial agent biosynthesis: The effect
of different environmental and nutritional factors on the antimicrobial activity
indicated that the maximum activities was obtained in starch nitrate broth medium
at, incubation period (10 days), incubation temperature (35°C), agitation
and aeration (160 rpm), pH value (8.0), carbon source (Starch), nitrogen source
(NaNO3), water soluble vitamin (vitamin H), inoculum age (12 days),
Fermentation and isolation of antimicrobial agent: The Streptomyces crystallinus, AZ151 inoculum was introduced aseptically into each sterile flask containing the following ingredients (g L-1): Arabinose, 20; NaNO3, 2.0; K2HPO4, 0.8; MgSO4.7H2O, 0.7; vitamin H, ppm and KCl, 0.5. The pH was adjusted at 8.0 before sterilization. After 10 days of incubation at 35°C filtration was carried out through filter paper Whatman No. 1 and followed by centrifugation at 5000 rpm for 15 min. Only clear filtrate was tested for its antimicrobial activity.
The clear filtrate containing the active metabolite, was adjusted at pH 7.0 then extraction process was carried out using Ethyl acetate at the level of 1:1 (v/v). The organic phase was collected and evaporated under reduced pressure using rotary evaporator. The residual material was dissolved in least amount of DMSO and filtered. The filtrates were test for their antibacterial activities. The antimicrobial agent was precipitated by petroleum ether (b.p. 60-80 EC) and centrifuged at 4000 r.p.m for 15 min. The fraction was test for antimicrobial activities. 8-10% (v/v), amino acid (Asparagine), MgSO4.7H2O concentration (0.7 g L-1), K2HPO4 (0.8 g L-1), inoculum size (8-10 % (v/v) and at inoculum culture age (12 days) (Table 3).
Separation of antimicrobial agent into individual components was carried out by thin-layer chromatography using a solvent system composed of chloroform and methanol (24:1, v/v). Among three bands developed, only one band at Rf 0.55 showed antibacterial activity. The purification process through column chromatography packed with silica gel, indicated that maximum activity was at fractions Nos. 14-23 (Fig. 3).
Physicochemical characteristics of the antimicrobial agent: The purified
antimicrobial agent produced by Streptomyces crystallinus, AZ151 produces
characteristic odour, its melting points is 160°C.
||The environmental conditions and nutritional requirements
affecting the biosynthesis of antimicrobial agent by Streptomyces crystallinus,
|*Mean values of triplicate determinations were calculated.
**SN: Starch nitrate medium, SC: Starch casein medium , YEME: Yeast extract
malt extract medium, GA: Glycerol asparagine medium, ISS: Inorganic salt
starch medium and TYE: Tryptone yeast extract medium
|| Antimicrobial activity of fractions for antimicrobial agent
|| IR spectrum of antimicrobial agent
The compound is freely soluble in chloroform, ethyl acetate, n-butanol, acetone,
ethyl alcohol, methanol and 10% isopropyl alcohol but insoluble in petroleum
ether, hexane and benzene.
Elemental analysis: The elemental analytical data of the antibacterial agent revealed the following data: C = 46.43; H = 7.46; N = 6.81; O = 39.43 and S = 0.0. This analysis indicates a suggested calculated empirical formula of C15H30N2O10.
Spectroscopic characteristics: The spectroscopic analysis of purified antimicrobial agent produced by Streptomyces crystallinus, AZ151 have been determined. The infrared (IR) spectrum showed characteristic band corresponding to 21 peaks (Fig. 4), the ultraviolet (UV) spectrum recorded a maximum absorption peak at 225 NM (Fig. 5) and the Mass spectrum indicate that the molecular weight was 432.36 (Fig. 6).
|| Ultraviolet absorbance of antimicrobial agent
|| Mass spectrum of antimicrobial agent
Identification of the antimicrobial agent: On the basis of the recommended keys for the identification of antibiotics and in view of the comparative study of the recorded properties of the antimicrobial agent, it could be stated that the antimicrobial agent is suggestive of being belonging to Hygromycin-B antibiotic (Table 4).
Biological activities of the antimicrobial agent: Data recorded in Table
5 indicated that the antimicrobial agent is fairly active against both,
Gram positive and Gram negative bacteria and unicellular and filamentous fungi.
|| A comparative study of characteristic properties of antimicrobial
agent in relation to Reference antibiotic (Hygromycin-B)
|| Minimum inhibitory concentration of the antimicrobial agent
The Minimum Inhibitory Concentration (MIC) of antibiotic produced by Streptomyces
crystallinus, AZ151 was determined and results showed that MIC (μg
mL-1) against Staphylococcus aureus (1.73), Klebsiella
pneumonia (3.9), Escherichia coli and Salmonella typhi (7.8),
for Aspergillus flavus and Alternaria alternata (31.25) and Saccharomyces
cerevisiae (62.5) (Table 5).
The aminoglycosides such as Hygromycin B are a large and diverse class of antibiotics
that characteristically contain two or more aminosugars linked by glycosidic
bonds to an aminocyclitol component. The cyclitol is 2-deoxystreptamine-streptomycin
which has a streptidine moiety (Umezawa and Hooper, 1982).
Soil, in particular, is an intensively exploited ecological inhabitant, of which,
produce many useful natural products, including clinically important antibiotics
(Waksman, 1961; Waksman, 1975).
Among soil inhabitants, actinomycetes and more specifically streptomycetes,
are of practical importance because they produce most of the useful natural
antibiotics for medical use. Nevertheless, selective isolation of soil actinomycetes
is important for understanding their ecological properties and for finding novel
strains which can produce useful bioactive secondary metabolites. Therefore,
various media and techniques have been developed for selective isolation of
actinomycetes (Hozzein et al., 2008). A total
6 actinomycetes were isolated from the soil sample through crowded plate technique
were subjected to primary screening and identified as Intrasporangium
sp., Dactyl sporangium sp., Micromonospora sp., Streptoverticillium
sp. and two Streptomyces sp. (Raja et al.,
In the course of searching for new actinomycetes producing antibiotics in our study, screening program has been conducted. The data presented in this study gave detail information on the isolation and identification of actinomycetes from various Egyptian localities e.g. (Assiut, Luxor and El-Minia governorates). The results indicated the highest percentage of isolation (43.2%), 84 isolates out of 194, were isolated on Starch Nitrate Agar (SNA) medium followed by (28.3%), 55 isolates on both starch casein agar and glycerol asparagine agar (data not shown).
The most active isolates, in terms of mean diameter of inhibition zone (mm), 74 (38%) was obtained against Staphylococcus aureus 90.5% (67) followed by Aternaria alternata 43.2% (32) and klebsiella pneumoniae, 41.8% (31) while the lowest percentage was obtained against Fusarium verticillioides 21.6% (16 isolates), Salmonella typhi 20.2% (15 isolates), Escherichia coli 9.4% (7 isolates), Aspergillus fumigatus 9.4% (7 isolates), Saccharomyces cerevisiae 8.1% (6 isolates) and Aspergillus flavus 6.7% (5 isolates).
Many other percentages were also found 100% (14) against Phytophthora megasperma,
followed by Alternaria solani and Alternaria alternata 78.5% (11)
while the lowest percentage was obtained against Fusarium solani and
Saccharomyces cerevisiae 14.2% (2) and 7.1% (1), respectively (Aghighi
et al., 2004). In addition, streptomycetes isolates appear to be
highly active against Gram-positive bacteria (Hamdi et
al., 1980; Hussein et al., 1981; Saadoun
et al., 1998).
Among our strains (194), an actinomycete isolates (AZ151) showed high potencies
against all microorganisms tested. Its morphological, physiological and biochemical
characteristics as well as, its color and culture characteristics have been
investigated. A similar study found that the highest percentage of active isolates
was red and gray series and the lowest in the green and white ones (Saadoun
et al., 1998). However, most antimicrobial producing species of streptomycetes
were found in the gray and yellow series of no chromomeric type and no antibiotic
produced by white and green series chromomeric type (Aria
et al., 1976). Antimicrobial sensitivity testing of these strains
was done by Kirby-Bauer disc diffusion method (Khan et
al., 2011). Minimum Inhibitory Concentration (MIC) of the extracts was
determined by the micro broth dilution against 14 clinical and standard strains
of methicillin resistant and sensitive of Staphylococcus aureus (Dadgar
et al., 2006). Over 110 soil actinomycetes isolates were screened
among which one isolate showed high level of activity in Agar disk and Well
diffusion methods against E. carotovora subsp. carotovora and
identified as a new strain of Streptomyces plicatus (strain 101) (Zamanian
et al., 2005).
The species belonging to the genus Streptomyces constitute 50% of the
total population of soil actinomycetes and 75-80% of the commercially and medicinally
useful antibiotics have been derived from this genus (Mellouli
et al., 2003). Over 110 soil actinomycetes isolates were screened
among which one isolate showed high level of activity in Agar disk and Well
diffusion methods against E. carotovora subsp. carotovora and
identified as a new strain of Streptomyces plicatus (strain 101) (Zamanian
et al., 2005).
The extract from culture filtrate of endophytic Streptomyces sp. ST8
by ethyl acetate has activity against S. mutans ATCC25175 and 104B.
The extract at such concentrations (0.05-5 mg mL-1) showed the inhibition
of bacterial adherence on glass surfaces and saliva-coated hydroxyapatite. The
crude extract also decreased the activity of glucosyltransferase and glucan-binding
lectin from both strains (Taechowisan et al., 2008).
Besides, selective isolation of soil actinomycetes is important for understanding
their ecological properties and for finding novel strains which can produce
useful bioactive secondary metabolites. Therefore, various media and techniques
have been developed for selective isolation of actinomycetes (Hozzein
et al., 2008).
In this study, we found the nucleotide sequence of the 16S rRNA gene (1.5 kb) of the actinomycete isolate, AZ151 evidenced a 92% similarity with Streptomyces crystallinus 16S rRNA genes. In addition, multiple sequence alignment was conducted the sequences of the 16S rDNA gene of Streptomyces crystallinus, (CHR and SNG). The sequencing product was determined as 1141 bp2). On the basis of theses data and in view of the comparative study of the recorded properties of AZ151 in relation to the most closest reference strain, viz. Streptomyces crystallinus, it could be stated that it is suggestive of being belonging to Streptomyces crystallinus which can produce a broad-spectrum antibiotic.
In addition, 16S rRNA sequence data have proved invaluable in Streptomycetes
systematics, in which they have been used to identify several newly isolated
Streptomyces (Mehling et al., 1995). This
finding is in agreement with that noticed of antibiotic phenazine derivatives
and their formation pathways in a new Streptomyces strain P510, where
culture characteristics and 16S rRNA nucleotide analysis confirmed strain P510
as Streptomyces griseoluteus (Wang et al.,
Several methods have been developed to identify Streptomyces species.
These include, culturing methods using the selective plating technique (Kuster
and Williams, 1964), construction of genetic marker systems (Wipat
et al., 1991), a combination of chemical markers, the presence of
LL diaminopimelic acid and the absence of characteristic sugars in the cell
wall (Lechevalier and Lechevalier, 1970; Atta
et al., 2011). Also, sensitivity to antibiotics and phages, serological
reactions and ecological properties has also been used for the classification
of Streptomyces spp. (Shirling and Gottlieb, 1966;
Lechevalier and Lechevalier, 1980).
The highest antimicrobial activity was achieved at optimum environmental and
nutritional conditions in Streptomyces crystallinus AZ151 culture. Several
studies have shown the optimization of nutritional and environmental conditions
for antibiotic production (Kumar and Satyanarayana, 2007;
Latifian et al., 2007; Gupta
et al., 2008; Kagliwal et al., 2009;
Atta et al., 2011). San et
al. (2010) worked on two venoms of Calloselasma rhodostoma and
Ophiophagus hannah and determined (MIC) with Staphylococcus aureus
ATCC25923, ATCC29213 and ATCC43300. The MIC values obtained for Calloselasma
rhodostoma were 125 μg mL-1 when tested against S. aureus
ATCC25923 and ATCC43300 while it was 250 μg mL-1 when tested
against S. aureus ATCC29213. MIC values obtained for Ophiophagus hannah
were 250 μg mL-1 when tested against all three strains.
In fact, the active metabolites were extracted by ethyl acetate (Criswell
et al., 2006; Sekiguchi et al., 2007;
Augustine et al., 2005). The extract from culture
filtrate of endophytic Streptomyces sp. ST8 by ethyl acetate has activity
against S. mutans ATCC25175 and 104 B. The extract at such concentrations
(0.05-5 mg mL-1) showed the inhibition of bacterial adherence on
glass surfaces and saliva-coated hydroxyapatite. The crude extract also decreased
the activity of glucosyltransferase and glucan-binding lectin from both strains
(Taechowisan et al., 2008).
The organic phase was collected and evaporated under reduced pressure using
rotary evaporator. Moreover, the purification process indicated that maximum
activity was recorded between fraction Nos. 14-23. Many workers used a column
chromatography packed with silica gel and the same situation was observed (Hitchens
and Kell, 2003; Criswell et al., 2006; Sekiguchi
et al., 2007).
In this study we determined the physico-chemical characteristics of the purified antimicrobial agents produced by Streptomyces crystallinus AZ151 and indicated that, it produces characteristic odour, its melting points is 160°C, infrared (IR) spectrum showed characteristic band corresponding to 21 peaks, a maximum absorption UV peak recorded at 225 NM and Mass spectrum confirmed that the molecular weight is at 432.36. Consequently, the elemental analytical data are find to be:
C = 46.43; H = 7.46; N = 6.81 and O = 39.3, indicate a suggested empirical
formula of C15H30N2O10 and being
belonging to Hygromycin-B antibiotic. Physico-chemical characteristics of many
antibiotics were determined (Koshiyama et al., 1969;
Singh and Gurusiddaiah, 1984; Omura
et al., 1987; Uyeda et al., 2001;
Yanai and Murakami, 2004; Atta et
al., 2011)." class="btn btn-success" target="_blank">View Fulltext
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