Retracted: Optimization, Composition, and Antioxidant Activities of Exo- and Intracellular Polysaccharides in Submerged Culture of Cordyceps gracilis (Grev.) Durieu & Mont.

[This retracts the article DOI: 10.1155/2015/462864.].

The concerns are as follows: (1) Figure 1(b) in each article presents the same photograph, though they are meant to represent different fungal species.(2) Tables 1 and 2 in each article show many exact digit matches between the articles for the polysaccharide yield means and standard errors, especially in Table 1, despite the results representing different species.
(3) The distribution of insignificant digits (i.e., digits unimportant to the measured value) is expected to be uniform [4].The decimal values in the polysaccharide yield means and standard errors in Tables 1 and 2 in the three articles have a significantly nonuniform distribution.(4) The scanned laboratory notebooks have no dates or signatures.The raw data for the polysaccharide yield replicates do match the published means and standard errors, but this means there is a perfect match between the means and standard errors for the IPS yields by temperature between the articles in Evidence-Based Complementary and Alternative Medicine and BMC Complement.Altern.Med, even though these results correspond to different values in the underlying data.The decimal values in the raw data for the IPS yields by temperature also have a significantly nonuniform distribution.(5) One of the Evidence-Based Complementary and Alternative Medicine article authors, Dr. Narender

Introduction
Cordyceps Fr. is a widespread genus with 400 species worldwide [1][2][3].Many species of this genus have been reported as the source of disease combating natural products with tremendous biological activities and considered as a rare and exotic medicinal fungus for centuries.Fruit bodies and mycelial extracts of this fungus have been found to exhibit different pharmacological activities [4].
Commercial cultivation through submerged culture is now becoming quite useful because of higher mycelial yield with fewer chances of contamination [33,34].EPS as well as IPS extracted from submerged culture possess the same biological activities [35].However, the productivity of polysaccharides has been found to vary with environmental conditions and medium composition, including carbon source, nitrogen source, and pH [36].In view of this, present studies were conducted to optimize the EPS and IPS production by one-factor-at-a-time method and orthogonal matrix method, monosaccharide composition and to evaluate the antioxidant activities of EPS and IPS in submerged culture of C. gracilis.

Extraction of EPS and IPS. Exopolysaccharides (EPS)
were extracted by the standard method with minor modifications [39].Briefly, mycelial biomass in the medium was centrifuged at 10,000 ×g for 12 min.The supernatant obtained was mixed with three volumes of pure ethanol and left for 24 hours at 4 ∘ C. The resulting precipitate was then separated by centrifugation at 8000 ×g for 10 min.The precipitate (EPS) was washed with ultrapure water and subsequently lyophilized for quantitative assessment and analysis.
For intracellular polysaccharides, mycelial biomass was subjected to extraction with boiling water for an hour and the mixture was filtered through Whatman number 1 filter paper.The filtrate was allowed to precipitate with four volumes of 95% (v/v) ethanol and left overnight at 4 ∘ C. The polysaccharides thus precipitated were separated by centrifugation at 8000 ×g for 10 min.The precipitates (IPS) were washed with ultrapure water and subsequently lyophilized for quantitative assessment and analysis [40].

Polysaccharides Composition.
Monosaccharide composition of polysaccharides was determined by high performance liquid chromatography coupled to an evaporative light scattering detector [41].Polysaccharide fraction (0.1 g) was extracted with 2.5 mL of 70% aqueous methanol followed by 1.5 mL of 70% aqueous methanol and then 1 mL of 70% aqueous methanol.This extract was centrifuged at 4000 rpm at 4 ∘ C for 10 min.Supernatant was collected and volume made up to 5 mL with 70% methanol.The extract was passed through Millipore filter (0.45 m) prior to injection on the HPLC.

DPPH Radical Scavenging Activity.
The DPPH scavenging activity was measured by the standard method described by Vamanu [42].Briefly, DPPH (200 m) solution at different concentrations (2-10 mg/mL) was added to 0.05 mL of the samples dissolved in ethanol.An equal amount of ethanol was added to the control.Ascorbic acid was used as the control.The absorbance was read after 20 min at 517 nm and the inhibition was calculated using the formula where  0 was the absorbance of the control and   was the absorbance in the presence of the sample.EC50 values were calculated using different sample concentrations (2-10 mg/mL) to obtain antiradical curves.Antiradical curves were plotted referring to concentration on the -axis and relative scavenging capacity on the -axis.EC50 values were calculated using the following equation: where log 0 is the center of the curve.

ABTS Radical Scavenging
Assay.ABTS radical scavenging activity was measured by the method described by Li et al. [43].For this, 10 L of the sample was added to 4 mL of the diluted ABTS •+ solution (prepared by adding 7 mM of the ABTS stock solution to 2.45 mM potassium persulfate, kept in the dark, at room temperature, for 12-16 h before use).
The solution was then diluted with 5 mM phosphate-buffered saline (pH 7.4) to an absorbance at 730 nm of 0.70 ± 0.02 [43].After the addition of 10 L of the sample to 4 mL of the diluted ABTS •+ solution, the absorbance was measured at 30 min.Ascorbic acid was used as control.The ABTS radical scavenging activity was calculated as Different sample concentrations (2-10 mg/mL) were used to obtain EC50 values.Standard curve was prepared with

R E T R A C T E D
Evidence-Based Complementary and Alternative Medicine 3 the sample concentration on the -axis and relative scavenging capacity on the -axis.EC50 values were calculated using the following equation: where log 0 is the center of the curve.
2.6.Reducing Power.Reducing power was estimated by the standard method given by Papuc et al. [44].Briefly, 200 L of the samples was mixed with sodium phosphate buffer (pH 6.6), 1 mM FeSO 4 , and 1% potassium ferricyanide and incubated for 20 min at 50 ∘ C; after that trichloroacetic acid was added and the mixtures were centrifuged.Supernatant (2.5 mL) was mixed with an equal volume of water and 0.5 mL 0.1% FeCl 3 .The absorbance was measured at 700 nm.
Reducing power of the samples was calculated using EC50 values with different sample concentrations (2-10 mg/mL).
Standard curve was made referring to concentration on the -axis and relative scavenging capacity on the -axis.EC50 values were calculated using the following equation: where log 0 is the center of the curve.

Ferrous Ion Chelating Assay.
For this, 1 mL of the sample (2-10 mg/mL) was mixed with 3.7 mL of ultrapure water, following which the mixture was reacted with ferrous chloride (2 mmol/L, 0.1 mL) and ferrozine (5 mmol/L, 0.2 mL) for 20 min.And the absorbance was read at 562 nm.EDTA was used as positive control.The chelating activity on the ferrous ion was calculated using the following formula: chelating activity (%) = [(  −   )/  ] × 100, where   is the absorbance of the blank and   is the absorbance in the presence of the extract [45].Chelating activity of samples was calculated using EC50 values with different sample concentrations (2-10 mg/mL) by standard curve referring to concentration on the -axis and chelating activity on the -axis.EC50 values were calculated using the following equation: where log 0 is the center of the curve.

Experimental Design.
Different factors considered for the orthogonal design were carbon sources, nitrogen sources, and ratio of carbon to nitrogen sources, temperature, pH value, medium capacities, rotation speed, and culture time.
According to the results of the single factor experiment, the orthogonal L 9 (3 4 ) was used for optimal culture conditions in submerged cultures.
2.9.Statistical Methods.All results are expressed as mean ± standard error. < 0.05 was considered significant, and SPSS software (SPSS Inc., Chicago, IL, USA) was used to calculate differences.All experiments were performed at least 3 times and with 3 replicates.The results were analyzed using one-way analysis of variance (ANOVA).Tests of significant differences were determined by Tukey-HSD at  < 0.05.[27,37].The results obtained under present experiments on the effect of rotation speed on polysaccharide production were the same as those obtained in C. ophioglossoides [37].Culture incubation time and pH range showed significant effect on EPS and IPS production.C. gracilis incubated for 6 days and pH 6.0 showed maximum EPS and IPS production (Table 1).

Results and Discussion
In the species, namely, C. ophioglossoides and C. sinensis, incubation period of 5-6 days and slightly acidic pH 5.0-6.0 promoted maximum IPS production [37,46].C. gracilis culture showed maximum EPS (405.24 ± 1.11 mg/L) and IPS (215.60 ± 1.71 mg/L) production at 23 ∘ C.This temperature for C. sinensis was observed as 20 ∘ C and, for C. ophioglossoides, it was found to be 25 ∘ C [37,47].Six different carbon sources were studied to find the suitable medium source for the production of EPS and IPS in Cordyceps gracilis.Although all the tested carbon sources yielded EPS and IPS, maximum EPS (464.82 ± 2.12 mg/L) and IPS (264.42 ± 2.62 mg/L) production took place in the medium supplemented with glucose as carbon source.Glucose was also found to be the most favorable carbon source for polysaccharide production in many of the Cordyceps species [37,48,49].To find the best nitrogen source, six different nitrogen sources were selected.Amongst them, yeast extract provided maximum EPS (465.21 ± 3.11 mg/L) and IPS (245.17 ± 3.24 mg/L) production.The results obtained under present studies are similar to those obtained from other researches [47].C/N ratio 10 : 1 promoted maximum EPS (395.29 ± 2.15 mg/L) and IPS (235.62 ± 1.40 mg/L) production for C. gracilis (Table 2).Present results are in conformity with previous reports on C. ophioglossoides, as C/N ratio 10 : 1 provided maximum IPS (653.79 ± 5.24 mg/L) production [37].
Monosaccharide composition of polysaccharides showed glucose in major percentage (62.15± 7.33%) followed by rhamnose (36.81 ± 4.57%) and galactose in minor quantities (0.10 ± 0.0%) (Table 3).Similar results were obtained for polysaccharide composition of C. militaris (L.) Link and other medicinal basidiomycetes, in which glucose was found to be the major monosaccharide along with sucrose and galactose [42,50].
Results obtained for influence of different factors on yield of EPS and IPS showed a significant positive effect.Results revealed the effect on EPS and IPS production in the order   4).

Antioxidant Activities of EPS and IPS.
The DPPH free radical scavenging activity of EPS and IPS extracted from the mycelium of C. gracilis showed positive and direct correlation with the concentration of the sample (Figure 1(c)).Both EPS and IPS extracted from C. gracilis showed high DPPH scavenging activity.However, EPS showed higher DPPH scavenging activity than IPS.The results are supported by EC 50 values, which were found to be 7.32 ± 0.09 mg/mL for EPS and 6.79 ± 0.04 mg/mL for IPS (Table 5).These results are in conformity with previous reports on other medicinally important species like C. militaris and C. sinensis [51,52].The inhibition percentage of the ABTS radical by EPS and IPS of C. gracilis was found to be directly dependent upon the concentration of the sample.The scavenging effect of all the extracts increased with increasing concentration as shown in the figure.At a concentration of 10.0 mg/mL, the percentage inhibition of EPS and IPS was found to be the same.High concentrations of the EPS and IPS are able to quench the free radicals in the system.The results indicated that the EPS and IPS of C. gracilis possessed significant scavenging power for the ABTS radicals (Figure 1(d)).
The results obtained for reducing power abilities of EPS and IPS in submerged culture of C. gracilis showed that both types of polysaccharides possessed the high reducing  ability.The reducing powers of EPS and IPS increased as the concentration increased (Figure 1(e)).However, the reducing power of EPS was found to be higher than the reducing power of IPS.At a concentration 10 mg/mL, maximum difference in the reducing power of EPS (1.23 ± 0.02 mg/mL) and IPS (0.73 ± 0.00 mg/mL) was observed.The reducing power of polysaccharides is due to the presence of reductones and present results showed that EPS and IPS of C. gracilis contained reductones which react with certain precursors of peroxides to prevent peroxide formation.The iron chelating ability of the EPS and IPS was found to be related with the concentration of sample.At initial concentration 2 mg/mL, there was not much difference between the iron chelating ability of both EPS (60%) and IPS (58%).However, at higher sample concentrations, EPS showed higher iron chelating ability than IPS (Figure 1(f)).Both EPS (80%) and IPS (60%) showed maximum iron chelating activity at a concentration 10 mg/mL.The results are further supported by EC 50 values (Table 5).EPS and IPS extracted from submerged culture of C. gracilis have shown significant antioxidant activities as reported in C. sinensis [53] and C. militaris [54].Since antioxidants are well known for playing important roles in the human metabolic system and for protecting against cardiovascular and neurodegenerative diseases, present investigations showed the medicinal value of the submerged culture of C. gracilis [55,56].

Conclusion
Results obtained under present investigations showed that Cordyceps gracilis is a medicinal fungus and it contained both EPS and IPS in appreciable amount.In vitro evaluation of antioxidant activities of EPS and IPS showed significant higher antioxidant activities.However, submerged cultivation of this fungus required several factors for the production of EPS and IPS.Factors such as temperature, rotation speed, pH, incubation time, carbon, nitrogen, and carbon to nitrogen ratio showed significant effect on the production of EPS and IPS.Due to significantly higher DPPH radical scavenging activity, ABTS radical scavenging activity, reducing power, and iron chelating abilities, this fungus is useful for its pharmaceutical applications.Present findings will open the scope for its large-scale industrial fermentations for commercial uses like other commercially explored Cordyceps species.

Figure 1 :
Figure 1: (a) Wild fruit body of C. gracilis on Hymenoptera insect.(b) Four-day-old mycelium on potato dextrose agar (PDA) medium.(c) DPPH scavenging activity of EPS and IPS.(d) ABTS radical scavenging activity of EPS and IPS.(e) Reducing power of EPS and IPS.(f) Iron chelating activity of EPS and IPS.

Table 1 :
Effect of different factors on EPS and IPS yield in submerged culture of C. gracilis.Values are expressed as mean ± SE and the same alphabets in the same column are not statistically significant according to Tukey's test for multiple comparisons with  < 0.05 for different conditions as mentioned in the table.

Table 2 :
Effect of different factors on EPS and IPS yield in submerged culture of C. gracilis.
aValues are expressed as mean ± SE and the same alphabets in the same column are not statistically significant according to Tukey's test for multiple comparisons with  < 0.05 for different conditions as mentioned in the table.

Table 4 :
Results obtained for orthogonal design.

Table 5 :
EC 50 values of EPS and IPS.