Research Article | Open Access
G. Sanjotha1, C.T. Shivasharana1 and Sudheer I. Manawadi2
1PG Studies in Biotechnology and Microbiology, Karnataka University, Dharwad, India.
2Department of Biotechnology, Government Arts and Science College, Karwar, India.
J. Pure Appl. Microbiol., 2019, 13 (4): 2261-2272 | Article Number: 5872
https://doi.org/10.22207/JPAM.13.4.40 | © The Author(s). 2019
Received: 23/09/2019 | Accepted: 30/11/2019 | Published: 18/12/2019
Abstract

Biosynthesis of kojic acid by fungi has been acquired huge attention nowadays because it can be used as an alternative method to chemically synthesized compounds. The fundamental feature of the microbiological agitation practice was to obtain potential fungi to achieve greater amount of kojic acid, the fungal isolate used in this study exhibited maximum growth on PDA and was identified as A.flavus based on its microscopic and macroscopic characteristics and ITS sequence analysis. In this vignette, appropriate cultivation conditions were carried out to gain a highest quantity of kojic acid. The maximum yield of kojic acid (31g/l) was reached by formulating the medium. The massive amount of kojic acid and maximum biomass was achieved from A. flavus by utilizing yeast extract as a nitrogen source and carbon source as glucose. The optimum incubation temperature employed was at 30oC, optimal pH was 3. Antagonistic activity was analyzed against both bacterial and fungal pathogens. The ethyl acetate extract exhibit increased antibacterial activity and maximum antifungal activity comparable with methanol, and chloroform.

Keywords

Aspergillus flavus, kojic acid, antimicrobial activity, optimization, dry biomass.

Introduction

Throughout evolution, an attempt was made to include marine microbes into the area of the pharmaceutical industry to discover new drugs1. Fungal isolates obtained from marine habitats have been identified as renowned producers of unique bioactive compounds2. Various Species of the genera Aspergillus have known repositories of antimicrobial substances with the highest efficiency3. The global health care system is facing the problem of multi-resistant microbes4-6. Most of the bacterial species exhibit antagonistic properties towards various antibiotics. In recent years, the majority of bacterial isolates such as S. aureus are exhibiting resistance mechanisms against ciprofloxacin, erythromycin, clindamycin7-10, Escherichia coli, Pseudomonas spp. and Klebsiella spp were involved in drug-resistant bacterial septicemia in Ile-Ife, Nigeria10 .

In the living cells, the chemical synthesis of kojic acid develops free radicals11. To overcome this consequence, several attempts have been made to choose a different approach to produce kojic acid. Recent investigations have concentrated on the isolation and usage of kojic acid from microorganisms as another non-toxic and secure method. In industry, biosynthesis of kojic acid from Aspergillus species is treated as one of the finest approaches12. More than 58 various species like Aspergillus, Penicillium, Mucor, etc, are used for Production of kojic acid13.

As far as the advancement of the potentiality of fungi to produce a considerable number of biologically active secondary metabolites that are involved in enhancement of ecological strength, and most of them perform the significant role as agents in defense mechanism, advancing regulators, insect attractants and as an agent for communicating with other organisms14. These pharmacologically active substances exhibit various properties such as antimicrobial, antitumor, antihyper-cholesterolemic, and Immunosuppressant15-19.

Additionally endophytic fungi are also renowned for the synthesis of similar bioactive metabolites from plants like Catharanthus alkaloids that are produced by endophytic fungi such as  campthothecin, vinblastine, vincristine and, paclitaxel these are potent drugs for cancer20, In such a way endophytic fungi  Aspergillus flavus influence prominent role in finding novel bioactive metabolites and they require very small quantity of substance from plants. In some tropical areas, maximum exposure of skin to sunlight can result in an elevated risk that leads to skin cancer, oxidative stress, and sunburn21. To prevent the hazardous cause of ultraviolet rays, kojic acid isolated from fungi has been used in many cosmetic creams, lotions, and soaps because they prevent hyperpigmentation and tyrosinase inactivity, it is also used to avoid food browning22.

Hence kojic acid and its derivatives have developed huge applications in medicine, Pharmaceutical industries, agricultural, chemical and food industries22. Along with kojic acid, its derivatives are also found to enhance solidity and solubilizing nature of kojic acid in various oily creams in the cosmetic industry23-26. Further other derivatives of kojic acid can have the capacity to inhibit tyrosinase activity and it has 8 times deeper potentiality than kojic acid24.

Some earlier reports have described as flufuran (5-(hydroxymethyl)-furan-3-carboxylic acid) is an isomer of kojic acid but recent studies indicates that flufuran was misidentified 27.

Kojic acid (5-hydroxy-2-hydroxymethyl-gamma- pyrone; KA) is synthesized from different microbes like fungi and some bacteria28,29. In the group of Aspergillus species, the oryzae-flavus- tamarii category is considered as the highest producer of kojic acid30. It is an essential secondary metabolite mainly obtained from carbohydrates. Kojic acid has wide applications in the medical field as an anti-inflammatory drug, it has been used as a pain killer, in the food industry it is utilized as an anti-speck, as a flavor enhancer, and in traditional foods, it gives special taste and color31,73. The purpose of usage of kojic acid in the agriculture field is that it acts as an anti-melanosis of agriculture products by preventing polyphenol oxidase formation32. Kojic acid exhibits bio-pesticide and bio- fungicidal activities in agriculture. In the agriculture field, it has been preferred for its biodegradable activity. It has various biological activities such as antibacterial, antifungal, antioxidant. It is also used as a whitening agent in the cosmetic industry33. Various microorganisms produce kojic acid as azidometalkojates form that exhibits antimicrobial activity. Besides, it acts as a chelating agent in insecticides production34,35.

Different carbon, nitrogen sources, pH and temperature can be employed for an adequate amount of kojic acid production. Until now, an ample amount of kojic acid has been obtained with the glucose that was used as a carbon source. Most of the Aspergillus and Penicillium species are potent producers of Kojic acid36.

Among Aspergillus species, Aspergillus flavus being attentive as the maximum producer of Kojic acid. Therefore the present survey was carried out to isolate and explore the antagonistic activity of biologically active compounds obtained from Aspergillus flavus and the results achieved were used to progress the control cultural strategy to produce maximum kojic acid.

Materials and Methods

Obtaining the fungi and its extracts
Soil samples were gathered from different regions in and around the coastal area of Karwar, Karnataka, India, during winter and summer seasons. Each sample was placed in sterilized tightly sealed polythene bags and brought to the laboratory for further investigation. Fungal isolates were separated by employing a serial dilution method on PDA medium supplemented with chloramphenicol (50ppm) to retard the growth of bacteria, incubated at 28°C at pH 6, for seven days, isolated colonies were grown separately.

Isolate that showed better growth was identified by using slide culture technique and lactophenol cotton blue staining technique and it was identified based on their morphological characteristics. Molecular characterization was carried out. Chromosomal DNA was extracted by using a spin column kit (Hi-Media, India or similar manufacturers. Fungal ITSrRNA gene (600 bp)37 amplification was carried out by using a PCR method in a thermal cycler and were purified using Exonuclease I – Shrimp Alkaline Phosphatase (Exo-SAP)38. Sanger method in ABI 3500xl genetic analyzer (Life Technologies, USA) was used to sequence purified amplicons. Sequencing files (.ab1) rearranged using CHROMASLITE (version 1.5) and further evaluated by Basic Local Alignment Search Tool (BLAST) with adjacent culture sequence recovered from the National Centre for Biotechnology Information (NCBI) database that locates a range of local analogy among sequences39. The program correlates protein or nucleotide sequences to database sequences and determines the statistical implication of similarities40. The BLAST algorithms deployed to interpret practical and progressive correlation among the sequences and it also helps to relate members of gene families. (i) Fundamental examination to search probably closely linked type strain sequences using the BLASTN program22 (ii) Pairwise arrangement to enumerate the sequence analogy values within the query sequence and the sequences identified in step (i)41. Therefore, each isolate is reported with the first five-ten hits observed in the said database. And the strain was identified and confirmed as Aspergillus flavus. Therefore further studies were conducted by employing A.flavus for the extraction of bioactive compounds. 

Production of kojic acid
The sterile 70ml medium in 250 ml Erlenmeyer flask employed for kojic acid production from 1ml of stock solution of A. flavus, (1 x 108 spore per ml) consisting of glucose (100 g/l); NaNO3 (2 g/l); KH2PO4 (1 g/l); MgSO4·7H2O (0.5 g/l); KCl (0.5 g/l); and FeSO4·7H2O (0.01 g/l). The culture was incubated at 30°C, 150rpm in incubator shaker for 30 days. Mycelium was separated by filtering through layers of sterile muslin cloth and then centrifuged at 6000rpm for 15min. Later Filtrate was transferred to the separating funnel containing ethyl acetate, chloroform, methanol (1:1 ratio) separately, aqueous and organic layers were separated followed by evaporation in a rotary evaporator. Kojic acid crystals were obtained by evaporation, these crystals were weighed and then placed in a clean vial42. Kojic acid concentration was determined against blank (the filtrate collected from the medium that is not inoculated) all the observations were used in triplicates.

Analytical determination of kojic acid and glucose
The analytical determination of glucose concentration was carried out by the DNS method43. Dinitrosalicyclic acid (DNS) reagent consisting of 3,5- dinitrosalicylic acid (10 g/l), phenol (2g/l), sodium sulfite (5 g/l) and NaOH (10g/l) was developed and 1ml of DNS reagent was added to 1ml of supernatant, boiled for 10min in boiling water bath, then it was cooled and 1ml of Rochelle salt was supplemented. The spectrophotometer was used to measure the absorbance at 575 nm.

The determination of the quantity of kojic acid was performed by a colorimetric method44. The experiment was conducted by mixing 1ml of supernatant with 1ml of ferric chloride (FeCl3) solution, which was prepared by placing FeCl3.6H2O (1gm) in 100ml of HCl (0.1N). The reddish color was formed due to the reaction between hydroxyl and phenolic functional groups present in the samples. The absorbance of the sample was estimated at 500nm by employing a spectrophotometer and used the kojic acid standard curve to determine the kojic acid equivalent.

Screening of antimicrobial activity
The extract obtained from the isolate was bioassayed for antibacterial and antifungal activity, this was analyzed by agar-based disk diffusion method45, against two gram-negative and two gram-positive bacteria and one fungal isolate. 0.2 ml of an overnight grown culture of target bacteria were inoculated on Nutrient agar medium, in similar fashion 0.2 ml of cultured target fungal isolate was on sabouraud’s agar medium. By using sterile spreader the two cultures were evenly spread out. A constant amount of 20µl of the extract of the isolate was applied on the sterile Whatman antibiotic assay discs of 6 mm diameter later located over the surface of the agar medium. Bacterial cultures were incubated at 37°C for 24h and fungal plates at 25°C for 72h. Diameters of inhibition zones were recorded. The analysis was achieved in duplicate.

Estimation of the dry weight of fungi
To determine the dry weight of the isolate the culture broth was drained through the sterile filter paper (Whatman 1). The mycelium was washed. The weight of the empty filter paper was measured, later weight was measured along with the fungal mycelium and then filter paper along with mycelium was placed in the oven at 95°C until the stable weight was reached, subsequently fungal dry biomass was measured46.

Analyzing the effect of nutritional conditions on kojic acid production
Different aspects were employed for the increased production of kojic acid. These aspects comprised:

The response of carbon source
Different kinds of carbon sources such as glucose, fructose, maltose, lactose, sucrose, starch, cellulose, xylose, arabinose were employed in the final concentration of carbon remained same (100g/l) in the medium, pH of the cultures were adjusted, were sterilized and incubated for 13 days in order to determine the prominence of carbon on kojic acid biosynthesis and increase of fungal biomass by measuring dry weight of mycelia. Analysis of kojic acid and the level of glucose was performed by colorimetric method44A. flavus utilize glucose as the prime source to manufacture a maximum quantity of kojic acid47. Glucose that acquired during the agitation process converts into kojic acid by the action of various enzymes associated with cell48,49 such as hexokinase and gluconate dehydrogenase, glucose-6-phosphate dehydrogenase, glucose is considered as the finest precursor for the maximum kojic acid synthesis.

The response of nitrogen source
The response of prominent nitrogen on kojic acid formation as well as increased biomass was determined by using different nitrogen sources such as ammonium nitrate, ammonium dihydrogen phosphate, ammonium mono hydrogen phosphate, yeast extract, asparagine, sodium nitrate, potassium nitrate at 0.2% w/v concentration was used.

The response of incubation temperature
Temperature plays a vitalizing role in the greatest recovery of kojic acid and the maximum yield of biomass. Different ranges of temperature 15, 20, 25, 30, 35, 40, 45°C were studied to understand the effect of temperature.

The Response of pH
The fermentation medium was adjusted to various pH ranging from 2, 3, 4, 5, 6, 7, 8 to examine the consequence of an action of pH on the improvement of kojic acid biosynthesis and dry mass.

RESULTS AND DISCUSSION

Microscopic observation and molecular characterization
Macroscopic, microscopic study (Fig. 1 and 2) and molecular identification revealed that the fungal isolate was belonging to the genus Aspergillus and it is confirmed that isolate was A. flavus. The Genbank Accession number is MK521427.

Fig. 1. Macroscopic examination of A. flavus.

Fig. 2. Microscopic examination of A. flavus.

Recovery of kojic acid and the estimation of biomass
The A.flavus was isolated for its potentiality to manufacture the highest kojic acid first on the PDA medium and then it was cultured on the production medium [glucose (100 g/l); NaNO3 (2 g/l); KH2PO4 (1 g/l); MgSO4·7H2O (0.5 g/l); KCl (0.5 g/l); and FeSO4·7H2O (0.01 g/l).] at 28±2°C. Kojic acid was extracted with ethyl acetate, chloroform and methanol (1:1 ratio), aqueous and organic layers were separated, evaporated in a rotary evaporator to acquire maximum 24.1g/l of kojic acid and increased dry weight 8.2 g/l with ethyl acetate extract, while kojic acid and dry mass from methanol extract was 20.4g/l and 7g/l, and from chloroform extract 14.3g/l and 6.5g/l was achieved. Hence ample amount of kojic acid and dry mass were obtained with ethyl acetate extract as the fermentation process progressed up to 13days. Such type of performance of kojic acid biosynthesis and dry mass by A.flavus was reported50-56.

Fig.3. Effect of various carbon source on synthesis of kojic acid drymass and consumption of sugar by A.flavus.

Fig. 4. Effect of different nitrogen source on synthesis of kojic acid drymass and consumption of sugar by A.flavus.

Previous studies described that several species and strains of Aspergillus genus such as A. flavusA. oryzae and A. parasiticus57-66 are potent producers of kojic acid. Some earlier results showed that A. flavus strain 44-1 acquire 32.50 g/l of kojic acid by employing rotary shaker66. Our results were comparable with reporter67 who demonstrated that an increased amount of kojic acid 39.9g/l was obtained by A. flavus strain 44-1 by applying SMF. Contrarily, a minimum level of kojic acid production 20 g/l by A. oryzae NRRL 484 in shake flask culture was reported68. However, the kojic acid biosynthesis by A. oryzae NRRL 484 was recorded28 as 24 g/l. After the recovery of kojic acid, it was estimated quantitatively by using the standard method44. The highest amount of kojic acid 24.1 g/l was attained by ethyl acetate extract by A.flavus when compared to methanol extract and from chloroform extract as shown in (Table 2). The vignette explores that the greatest quantity of kojic acid was synthesized by A. flavus whereas Aspergillus tamarii produces less quantity of kojic acid49 (15.2 g/l).

Table (1):
Characteristics of A. flavus.

Criteria Characteristics
Macroscopic  observation Colony on PDA media, after seven days of incubation at 28±20C shows 46 mm in diameter. Velvety, yellow to green or dark green, Reverse hyaline, goldish to red brown.
Microscopic observation Conidial heads are radiate and conidiophores are uncolored and Varying in length, commonly rough, hollow, and spiny in nature.
Microscopic morphology of phialides Both Uni-seriate and bi-seriate, whole vesicle is covered with phialides, extend in all directions


Antagonistic property of A. flavus
Kirbey-Bauer antibiotic testing (Agar based disk diffusion) method was carried out to test the antagonistic activity of the isolate against E. coli (MTCC 1687), P. aeroginosa (MTCC 1688), S. aureus (MTCC 96), B. subtillis (MTCC 441), A.flavus exhibit maximum zone of inhibition with crude ethyl acetate extract when compared to methanol extract and chloroform extract showed minimum zone of inhibition and chloramphenicol was used as control (Table 1). Antifungal activity by the isolate was conducted against C. albicans that was comparable with fluconazole as a standard antibiotic (Table 2). The diameter of the zone of inhibition was measured and was taken as a sensitivity test of bacteria and fungi.

Table (2):
Extraction solvents for the biosynthesis of kojic acid and dry mass by A.flavus.

Extraction Solvents Kojic acid (g/l) Dry mass (g/l)
Ethyl acetate 24.1 8.2
Methanol 20.4 7.0
Chloroform 14.3 6.5

Table (3):
Bioactivity of crude extracts of A.flavus against four bacterial pathogens.

Zone of inhibition in mm
Solvents Ec 1mg/ml Pa 1mg/ml Sa 1mg/ml Bs 1mg/ml Ch 1mg/ml
Ethyl acetate 20±0.1 19±0.2 20±0.1 21±0.7 23±0.7
Methanol 16±0.5 14±0.8 17±0.3 18±0.1 22±0.4
Chloroform 13±0.4 15±0.3 12±0.6 15±0.8 21±0.2

Table (4):
Bioactivity of crude extracts of A.flavus against fungal pathogen.

Zone of inhibition in mm
Solvents Ca 1mg/ml Fc 1mg/ml
Ethyl acetate 19±0.5 24±0.4
Methanol 14±0.1 22±0.7
Chloroform 11±0.2 21±0.2

The zone of inhibition of each extracts were expressed as the mean ± standard deviation. Ca-Candida albicans, Fc- Fluconazole

Table (5):
Effect of various carbon source on synthesis of kojic acid, drymass and consumption of sugar by A.flavus.

Carbon source Kojic acid g/l Dry weight g/l Sugar consumed g/l Residual sugar g/l Kojic acid/ sugar consumed g/l
Glucose 30.1 8.2 60 40 0.5
Sucrose 28.3 8 72 28 0.39
Fructose 25.2 7.6 84 16 0.3
Maltose 17.1 2 0 100 0
 Lactose 18.4 7.5 87 13 0.21
Starch 14.7 3 0 100 0
Cellulose 0 0 0 100 0
 Xylose 0 0 0 100 0
 Arabinose 0 0 0 100 0


Optimization conditions on kojic acid production by A. flavus
The kojic acid production by A. flavus was achieved by optimizing cultural conditions like carbon source, nitrogen source, incubation temperature and pH of the medium. To test the effect of carbon sources on the formulation of kojic acid and mycelia, different carbon sources were supplemented separately to the medium in constant concentration (100g/l). The outcome of the present work showed in (Table 5) indicates that the perfect carbon source for synthesis of kojic acid with dry mass was glucose (30.1g/l) and (8.2g/l) subsequently sucrose, fructose, lactose (28.3, 25.2, 18.4 g/l respectively) (8, 7.6, 7.5g/l respectively). According to some workers49,70,59, the structure of glucose is almost identical to kojic acid, during the fermentation process, direct conversion of glucose to kojic acid without the formation of smaller fragments will occur. Among the groups of carbon sources glucose, fructose, sucrose, and lactose exhibit the maximum amount of kojic acid and dry mass by a mold A.flavus when compared to maltose, starch, cellulose, xylose, and arabinose. In agreement with this report various kojic acid synthesizing strains utilize glucose, sucrose, and fructose as a carbon source to obtain 0.5 to 0.6 g of kojic acid per g of glucose70. Hence glucose is considered as both precursors for kojic acid biosynthesis and mycelial growth69,70.

Fig. 5. Effect of incubation temperature on kojic acid production, drymass and consumption of sugar by A.flavus.

Fig. 6. Effect of pH on kojic acid synthesis, drymass and consumption of sugar by A.flavus.

Among the various factors regulating the biosynthesis of kojic acid, the optimal source of nitrogen is a major component. The effect of nitrogen displayed in (Table 6) indicates that yeast extract, ammonium nitrate, and ammonium dihydrogen phosphate were the prominent nitrogen sources for manufacturing kojic acid (30.4, 24.3, 15.6 g/l respectively) with the consumption of glucose (81,73, 68 g/l respectively) and the dry biomass were (8.5,5.1,4.7 g/l respectively). The increased amount was obtained when yeast extract was used as a source of nitrogen with consumed glucose (81g/l). Our results were parallel with reporters who explained that the immobilized cell cultures exhibit consumption of glucose and the progression of kojic acid synthesis was maximum and are proportional with the rise in nitrogen concentration but at increased concentration, production of kojic acid was reduced and consumption of glucose was highest71.

Table (6):
Effect of different nitrogen source on synthesis of kojic acid drymass and consumption of sugar by A.flavus.

Nitrogen source Kojic acid g/l Dry weight g/l Glucose consumed g/l Residual glucose g/l Kojic acid/ Glucose consumed g/l
An 24.3 5.1 73 27 0.33
Adp 15.6 4.7 68 32 0.22
Ye 30.4 8.5 81 19 0.37
Amhp 10.3 4.2 58 42 0.17
As 7.1 4 79 21 0.08
Sn 0 0 0 100 0
Pn 1 0 0 100 0

An-Ammonium nitrate, Adp- Ammonium dihydrogen phosphate, , Ye- yeast extract, Amhp-Aammonium mono hydrogen phosphate,As- Asparagine, Sn- sodium nitrate, Pn- potassium nitrate

Temperature plays a leading role in mycelial growth and kojic acid synthesis by potential A.flavus was appeared at 30°C (30.1g/l) and dry biomass weight reached (8.2g/l). Some investigators showed that 25-30°C was the optimal temperature for the manufacturing of kojic acid by various fungi. 71

Table (7):
Effect of incubation temperature on kojic acid production, drymass and consumption of sugar by A.flavus.

Temperature oC Kojic acid g/l Dry weight g/l Glucose consumed g/l Residual glucose g/l Kojic acid/ Glucose consumed g/l
15 10.2 2.3 54 46 0.18
20 12.5 3.1 59 41 0.21
25 26.1 5.6 74 26 0.35
30 30.1 8.2 83 17 0.36
35 20.6 4.5 78 22 0.26
40 3 2.7 41 59 0.07
45 0 1 0 100 0

Various ranges of pH were employed to achieve the greatest kojic acid and the highest level of mycelial growth by A.flavus. The potential fungi A.flavus showed better growth at pH 3 to 5 (7.5, 8.4, 7.1 g/l) on the contrary at pH 6 to 8 the growth was completely reduced (5.2, 2, 1 g/l) while, biosynthesis of increased quantity of kojic acid (31.5 g/l) was obtained with maximum consumption of glucose (86 g/l ) at pH 3 however the amount of kojic acid was gradually decreased at pH s 4, 5, 6 and pH 7 and 8 production was entirely nil as displayed in (Table 8). Our results are coinciding with the results72,28 reported that the strains, A. flavus, A. parasiticus, and A. oryzae exhibit optimum pH values 4.5, 6.2, 6.5 for the secretion of kojic acid. Comparably, A. oryzae produces kojic acid at pH 473, in contrast, the kojic acid values appeared in our investigation were not consistent with other reporters, in which the largest amount of kojic acid was obtained from glucose at very acidic pH (1.9 to 3.0)74. During growth progress at pH 4.5 to 6, the fungi use enzymes to convert glucose into kojic acid36. However, the growth of the fungi was continuous at pH between 2 and 3 the production of kojic acid appeared75. The change in the outcome of our vignette with the values of earlier results can be described by the changes in the utilization of carbon and the nitrogen source. The most favorable pH for kojic acid is controlled by the kind of carbon and nitrogen source employed in the fermentation medium76.

Table (8):
Effect of pH on kojic acid synthesis, drymass and consumption of sugar by A.flavus.

pH Kojic acid g/l Dry weight g/l Glucose consumed g/l Residual glucose g/l Kojic acid/ Glucose consumed g/l
2 19.8 4.2 75 25 0.26
3 31.5 7.5 86 14 0.36
4 27.2 8.4 78 22 0.34
5 19.7 7.1 65 35 0.3
6 9.5 5.2 48 52 0.19
7 0 2 0 100 0
8 0 1 0 100 0

Apart from Kojic acid various fungal isolates produce some other organic acids, according to some investigators, organic acids such as Malic acid (50.5M) from (Aspergillus flavus)77, Itaconic acid (87.32g/l )from (Aspergillus terreus)78,  Cyclopiazonic acid from (Aspergillus tamarii)79 and (Aspergillus flavus)80 are obtained from several species of Aspergillus.

Besides, most of the plants are also notable for the production of various organic acids, for example, Tartaric, Citric, Malic, Lactic, Succinic, Acetic, Oxalic acids81, some Malus species generously incorporated malic acid and citric acid82, there are no shreds of evidence for kojic acid production from plants.

CONCLUSION

The present investigation was focused to optimize cultural conditions to synthesize maximum kojic acid from A.flavus. Glucose and yeast extract were the optimal carbon and nitrogen sources. Kojic acid can be obtained by employing other carbon sources like sucrose, fructose, and lactose. The optimum incubation temperature was 30°C and pH 3 (31.5 g/l ). Hence, in the present work, authors attribute kojic acid production from marine Aspergillus flavus, and compared to other acids, Kojic acid achieved from Aspergillus species has wide applications in various fields. Additionally, further investigation is needed to boost human power to fight with various microbial diseases.

Declarations

ACKNOWLEDGMENTS
We wish to thank Microbial Type Culture Collection and Gene Bank (MTCC), is funded by the Department of Biotechnology (DBT) and the Council of Science and Industrial Research (CSIR), Government of India, for providing different strains. We would like to express sincere thanks P.G Department of studies in Biotechnology and Microbiology, Karnataka University, Dharwad, Karnataka for providing facilities.

CONFLICT OF INTEREST
The authors declare that there is no conflict of interest.

AUTHORS’ CONTRIBUTION
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.

FUNDING
None.

ETHICS STATEMENT
This article does not contain any studies with human participants or animals performed by any of the authors.

AVAILABILITY OF DATA
All the data accomplished in the time of this research are incorporated in the manuscript.

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