Transformation of Litchi Pericarp-Derived Condensed Tannin with Aspergillus awamori

Condensed tannin is a ubiquitous polyphenol in plants that possesses substantial antioxidant capacity. In this study, we have investigated the polyphenol extraction recovery and 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity of the extracted polyphenol after litchi pericarp is treated with Aspergillus awamori, Aspergillus sojae or Aspergillus oryzae. We have further explored the activity of A. awamori in the formation of condensed tannin. The treatment of A. awamori appeared to produce the highest antioxidant activity of polyphenol from litchi pericarp. Further studies suggested that the treatment of A. awamori releases the non-extractable condensed tannin from cell walls of litchi pericarp. The total extractable tannin in the litchi pericarp residue after a six-time extraction with 60% ethanol increased from 199.92 ± 14.47–318.38 ± 7.59 μg/g dry weight (DW) after the treatment of A. awamori. The ESI-TOF-MS and HPLC-MS2 analyses further revealed that treatment of A. awamori degraded B-type condensed tannin (condensed flavan-3-ol via C4–C8 linkage), but exhibited a limited capacity to degrade the condensed tannin containing A-type linkage subunits (C4–C8 coupled C2–O–C7 linkage). These results suggest that the treatment of A. awamori can significantly improve the production of condensed tannin from litchi pericarp.


Introduction
Litchi (Litchi chinensis Sonn.), as a subtropical to tropical fruit with high commercial value, is widely planted in south China and Southeast Asian countries, as well as in African countries. It has attractive red-colored pericarp tissue that contains a significant amount of polyphenols [1]. Polyphenols have strong antioxidant activity, inhibit glucosidase and acetylcholinesterase [2], increase lifespan and stress resistance [3], block acetyl cholinesterase [2], alleviate the depressant effect [4] and reduce glucose-induced oxidative cell damage and dysfunction in pancreatic cell [5]. Previously, epicatechin, procyanidin A2, condensed tannin, cyanidin-3-rutinoside and rutin have been identified as the major polyphenols in litchi pericarp [6]. Solvent extraction of polyphenols from litchi pericarp has often

Effect of Aspergillus Treatments on Polyphenol Recovery and DPPH Radical Scavenging Activity
The effects of the Aspergillus treatment on the polyphenol extraction recovery from litchi pericarp and the antioxidant activity of the extracted polyphenol are shown in Figure 1. The polyphenol extraction recovery with aqueous-organic solvent extraction dramatically increased after litchi pericarp was treated with Aspergillus. The treatment of three fungi all significantly increased the phenolic contents both in the water fraction and ethyl acetate fraction. Since a large amount of polyphenols is conjugated to polysaccharide of cell walls or proteins in the cell membrane, it would be difficult to extract these polyphenols with aqueous-organic solvent [8]. Several hydrolytic enzymes produced by A. awamori, A. sojae and A. oryzae [18][19][20] likely released non-extractable polyphenols from litchi pericarp, thus increasing the extract recovery of the polyphenols. These hydrolytic enzymes may further hydrolyze glycosidic flavonoids to produce more hydrophobic aglycone in the ethyl-acetate fraction, which accounted for the enhanced DPPH radical scavenging activity of the fraction after the Aspergillus treatment. Furthermore, the hydrophobic products after the treatment of A. awamori exhibited higher DPPH radical scavenging activity than those treated with A. oryzae or A. sojae. Our previous study indicated that A. awamori had a great activity to cleave glycosidic bonds in rutin to form quercetin-3-glucoside and quercetin [15]. Additionally, the treatment of Peronophythora litchii with Colletotrichum gloeosporioides or Fusarium proliferatum was also conducted, which exhibited a high ability to increase the recovery of polyphenols from litchi pericarp, but with a low antioxidant activity (data not shown). with Aspergillus treatment and their DPPH radical scavenging activities (C). Data marked with the same letter above columns were not significant difference at p < 0.05 (mean ± SD, n = 3).

HPLC Analysis
The products of litchi pericarp after the treatment with A. oryzae, A. sojae or A. awamori were further analyzed by HPLC. The HPLC profiles are presented in Figure 2. As shown in the figure, Peaks 6, 11, 13, 14 and 15 were the major compounds present in the hydrophilic extract fraction of litchi pericarp without the fungus treatments, while Peaks 1', 2', 3', 4', 6' and 7' appeared in the hydrophobic extract fraction of litchi pericarp after the fungus treatment. In comparison with standard compounds, Peaks 6', 11', 7' and 8' were identified as procyanidin B2, epicatechin, -quercetin-3-glucoside and quercetin, respectively, which is consistent with the previous report [6,21]. The retention time of Peak 15 was matched with that of standard epicatechin-3-gallate, which is in agreement with the observation by Zhang et al. [21]. However, epicatechin-3-gallate was not detected in Sarni-Manchado's report [6], likely because a different cultivar of litchi was used in these studies. The Huaizhi cultivar was used in Zhang's study, while cultivar Kwai Mi was chosen in Sarni-Manchado's. The same plant materials used in Zhang's study were used in the present study. A large amount of compounds was eluted as a multi-overlapped peak at the retention time of 15-35 min, which is in agreement with the report by Roux et al. [22], who demonstrated the hump as condensed tannin with different degrees of polymerization. The area of Peak 6 decreased significantly after treatment with fungi, indicating that procyanidin B2 may be converted to other compounds. However, the area of Peak 11 (epicatechin) did not increase, possibly because procyanidin B2 was transformed to other flavonoids [23]. The HPLC profiles of the products of litchi pericarp after the treatment with A. oryzae were similar to that with the treatment of A. sojae (Peaks 1, 2, 4, 5, 7 and 9), indicating that A. oryzae and A. sojae may share similar enzymes [24]. with Aspergillus treatment and their DPPH radical scavenging activities (C). Data marked with the same letter above columns were not significant difference at p < 0.05 (mean˘SD, n = 3).

HPLC Analysis
The products of litchi pericarp after the treatment with A. oryzae, A. sojae or A. awamori were further analyzed by HPLC. The HPLC profiles are presented in Figure 2. As shown in the figure, Peaks 6, 11, 13, 14 and 15 were the major compounds present in the hydrophilic extract fraction of litchi pericarp without the fungus treatments, while Peaks 1', 2', 3', 4', 6' and 7' appeared in the hydrophobic extract fraction of litchi pericarp after the fungus treatment. In comparison with standard compounds, Peaks 6', 11', 7' and 8' were identified as procyanidin B2, epicatechin, -quercetin-3-glucoside and quercetin, respectively, which is consistent with the previous report [6,21]. The retention time of Peak 15 was matched with that of standard epicatechin-3-gallate, which is in agreement with the observation by Zhang et al. [21]. However, epicatechin-3-gallate was not detected in Sarni-Manchado's report [6], likely because a different cultivar of litchi was used in these studies. The Huaizhi cultivar was used in Zhang's study, while cultivar Kwai Mi was chosen in Sarni-Manchado's. The same plant materials used in Zhang's study were used in the present study. A large amount of compounds was eluted as a multi-overlapped peak at the retention time of 15-35 min, which is in agreement with the report by Roux et al. [22], who demonstrated the hump as condensed tannin with different degrees of polymerization. The area of Peak 6 decreased significantly after treatment with fungi, indicating that procyanidin B2 may be converted to other compounds. However, the area of Peak 11 (epicatechin) did not increase, possibly because procyanidin B2 was transformed to other flavonoids [23]. The HPLC profiles of the products of litchi pericarp after the treatment with A. oryzae were similar to that with the treatment of A. sojae (Peaks 1, 2, 4, 5, 7 and 9), indicating that A. oryzae and A. sojae may share similar enzymes [24].

The Effect of A. awamori Treatment on Condensed Tannin
The contents of total tannin and the mean polymerization of tannin extracted from litchi pericarp after the A. awamori treatment were analyzed. To evaluate non-extractable condensed tannin, treatment of A. awamori on the extracted residue of litchi pericarp was also conducted. As shown in Figure 3, the content of total tannin increased significantly from 1286.58 ± 13.87-1456.12 ± 15.73 μg/g DW when whole litchi pericarp powder was treated with A. awamori and from 199.92 ± 14.47-318.38 ± 7.59 μg/g DW when the extracted litchi pericarp residue was treated with A. awamori. The mean polymerization degree also increased significantly after the treatment of A. awamori, suggesting that the high polymerized condensed tannin is bound to the cellular wall via a conjugation or physical force to form non-extractive condensed tannin [25,26].

The Effect of A. awamori Treatment on Condensed Tannin
The contents of total tannin and the mean polymerization of tannin extracted from litchi pericarp after the A. awamori treatment were analyzed. To evaluate non-extractable condensed tannin, treatment of A. awamori on the extracted residue of litchi pericarp was also conducted. As shown in Figure 3, the content of total tannin increased significantly from 1286.58˘13.87-1456.12˘15.73 µg/g DW when whole litchi pericarp powder was treated with A. awamori and from 199.92˘14.47-318.38˘7.59 µg/g DW when the extracted litchi pericarp residue was treated with A. awamori. The mean polymerization degree also increased significantly after the treatment of A. awamori, suggesting that the high polymerized condensed tannin is bound to the cellular wall via a conjugation or physical force to form non-extractive condensed tannin [25,26].

ESI-TOF-MS
Next, the products of litchi pericarp after the treatment of A. awamori were subjected to the ESI-TOF-MS analysis. The MS spectra are presented in Figure 4. Some peaks were doubly-charged molecules, as the difference of the nearby isotopic ion peak was 0.5 Da. After litchi pericarp was treated with A. awamori, many quasi-molecular ion peaks were missing, indicating the transformation of condensed tannin. Condensed tannins are oligomers and polymers of flavan-3-ols [8], and epicatechin is the major flavonoid in litchi pericarp [6,27]. These subunits may be condensed via a C4-C8 (B type) or C4-C8 coupled C2-O-C7 (A type) manner to form an oligomer or polymer. As the m/z value of the quasi-molecular ion was determined by the number of positive ion in each subunit, the number of each subunit can be estimated by comparing the calculated molecular weight with the m/z value observed from the MS spectra ( Figure 4).
The m/z values for both A. awamori-treated and non-treated products obtained from the MS spectra and the proposed subunit are listed in Table 1. In this case, the polymerization degree of condensed tannin was 2-18 [27], and the major condensed tannin was the B-type epi/catechin hexamer (m/z 887.2 × 2), but epi/afzelechin and gallocatechin subunits were also observed. These results were somewhat different from the previous studies [28,29], possibly due to the different litchi cultivar used. Epi/afzelechin is a flavan-3-ol, which exhibits significant anti-inflammatory, analgesic and diuretic properties [30]. The 'Huaizhi' litchi employed in this study is the widest planted cultivar in south China. Our results indicated that the 'Huaizhi' cultivar can be used as the major source for epi/afzelechin. After the treatment of A. awamori, several peaks (m/z 579.3, 887.2, 1031.2, 1175.2, 1319.3, 1463.3 and 1751.4) disappeared, indicating the degradation of condensed tannin. Additionally, A. awamori treatment showed a high potential to degrade B-type condensed tannin (m/z 887.2), but a limited capacity to degrade those condensed tannin containing the A-type linkage subunit. The degradation of condensed tannins by gut microorganisms was reported previously [31,32]. It would be interesting to investigate the mechanism by which tannin is degraded by Aspergillus.

ESI-TOF-MS
Next, the products of litchi pericarp after the treatment of A. awamori were subjected to the ESI-TOF-MS analysis. The MS spectra are presented in Figure 4. Some peaks were doubly-charged molecules, as the difference of the nearby isotopic ion peak was 0.5 Da. After litchi pericarp was treated with A. awamori, many quasi-molecular ion peaks were missing, indicating the transformation of condensed tannin. Condensed tannins are oligomers and polymers of flavan-3-ols [8], and epicatechin is the major flavonoid in litchi pericarp [6,27]. These subunits may be condensed via a C4-C8 (B type) or C4-C8 coupled C2-O-C7 (A type) manner to form an oligomer or polymer. As the m/z value of the quasi-molecular ion was determined by the number of positive ion in each subunit, the number of each subunit can be estimated by comparing the calculated molecular weight with the m/z value observed from the MS spectra ( Figure 4).
The m/z values for both A. awamori-treated and non-treated products obtained from the MS spectra and the proposed subunit are listed in Table 1. In this case, the polymerization degree of condensed tannin was 2-18 [27], and the major condensed tannin was the B-type epi/catechin hexamer (m/z 887.2ˆ2), but epi/afzelechin and gallocatechin subunits were also observed. These results were somewhat different from the previous studies [28,29], possibly due to the different litchi cultivar used. Epi/afzelechin is a flavan-3-ol, which exhibits significant anti-inflammatory, analgesic and diuretic properties [30]. The 'Huaizhi' litchi employed in this study is the widest planted cultivar in south China. Our results indicated that the 'Huaizhi' cultivar can be used as the major source for epi/afzelechin. After the treatment of A. awamori, several peaks (m/z 579.3, 887.2, 1031.2, 1175.2, 1319.3, 1463.3 and 1751.4) disappeared, indicating the degradation of condensed tannin. Additionally, A. awamori treatment showed a high potential to degrade B-type condensed tannin (m/z 887.2), but a limited capacity to degrade those condensed tannin containing the A-type linkage subunit. The degradation of condensed tannins by gut microorganisms was reported previously [31,32]. It would be interesting to investigate the mechanism by which tannin is degraded by Aspergillus. 6       * The molecular weight of the proposed quasi-molecular ion peaks can be calculated with the following equation: molecular weight = CH (2 + H + 23Na + 39K + 272Af + 288Ca + 304Ga´2AL). CH is the charge of quasi-molecular ion, and AL and GS stand for the number of A-type linkage subunits and the number of gallate flavan-3-ol subunits, while Af, Ca and Ga are the number of epi/afzelechin, epi/catechin and epi/gallocatechin subunits, and T and NT mean A. awamori-treated and non-A. awamori-treated samples, respectively.

Phloroglucinolysis Analysis of Condensed Tannin
To further illustrate the effect of the treatment of A. awamori on condensed tannin, the product was subjected to HPLC-ESI-MS 2 analysis. As shown in Figure (Table 1). However, those peaks observed in the MS 2 spectra of Compound H could be contributed by the dehydrogenated products of the A-type dimer and an epi/catechin monomer. It is hard to differentiate between these two compounds with MS spectra because they had a similar chemical structure and shared many fragmentation ions in the MS 2 spectra [35]. However, this dehydrogenated product was not reported in litchi pericarp before, while the epi/catechin trimer containing both the A-type and B-type linkage has been reported [28]. Thus, Compounds H and D are more likely to be epi/catechin trimers containing both the A-type and B-type linkage and its phloroglucinol adduct derivate, respectively, rather than the dehydrogenated products. Furthermore, Compounds E, F, G, I and J were determined to be the phloroglucinol adduct of afzelechin, the phloroglucinol adduct of the epi/catechin A-type dimer, epicatechin, the epi/catechin A-type dimer, procyanidin A2 and the epi/catechin A-type dimer, respectively [25,34]. These compounds of litchi pericarp were largely composed of epi/catechin with the A-type or B-type linkage. A minor afzelechin subunit was also detected. After the incubation, the proportion of extension subunits decreased while the terminal subunits increased. The B-type linked (C4-C8) moiety in condensed tannin (Peak A) was likely cleaved by A. awamori to produce terminal subunits (Peak G, epicatechin). The proportion of the A-type dimer extension subunit (Peak F) decreased while the A-type dimer terminal subunit (Peaks H, I and J) increased concurrently, possibly because A. awamori cannot degrade the A-type oligomer. In addition, the B-type linkage may be conversed to the A-type linkage by laccase [36] or radical oxidation [37], which may account for the increased A-type subunits.

Plant Materials and the Starter Microorganisms
Fresh fruit of litchi (Litchi chinensis Sonn.) cv. Huaizhi was harvested from a commercial orchard in Guangzhou, China. The fruit was peeled manually. The pericarp was collected, then dried in open air and finally ground into powder. A. awamori, A. sojae and A. oryzae were obtained from Guangdong Culture Collection Center, Guangzhou, China. After being cultured on potato dextrose agar at 30˝C for 3 days, the spores were collected by washing the agar surface with 20 mL of sterile distilled water containing 0.1% Tween 80. The spores were counted using a haemocytometer, and the spore suspension was prepared with a final concentration of ca. 10 6 /mL and served as inoculums for the further experiments.

Incubation of Aspergillus on Litchi Pericarp
Litchi pericarp powder (LPP, 25 g) was weighted into 500-mL flasks and then sterilized at 121˝C for 20 min. Fresh spore suspension (1 mL, ca. 10 6 spores/mL) or the sterilized spore suspension was added into the flasks and then maintained at 30˝C for 6 days by stirring. The Aspergillus-treated LPP was extracted with 125 mL of 60% ethanol 3 times under the ultrasonic condition (210 W, 30˝C, 40 min). The ethanol was evaporated under vacuum at 50˝C, and then, the product was extracted two times with ethyl acetate (50 mL). The extractive phase was dried under vacuum and re-dissolved into 100 mL of ethanol. The affiant phase was evaporated to a final volume of 100 mL. To evaluate the effect of Aspergillus on the non-extractable condensed tannin, the incubation of Aspergillus with the LPP residue after 6 times of extraction with 60% ethanol was conducted. The total tannin content and mean polymerization degree of Aspergillus-treated and non-Aspergillus-treated LPP, as well as the LPP residue were comparatively analyzed. The experiments were conducted with triplicate biological repeats.

Incubation of Aspergillus with the Purified Condensed Tannin
To further reveal the change in the structure of condensed tannin after the application of Aspergillus, incubation on the purified condensed tannin was carried out. The litchi condensed tannin was extracted and purified with the following procures. LPP (50 g) was extracted 3 times using a solution of an acetone/water (70/30, v/v) mixture containing 0.1% vitamin C. After filtration, the acetone was removed under vacuum at 40˝C. The crude tannin was obtained after degreasing with 150 mL of n-hexane 3 times, and then, small molecular polyphenol was removed with 150 mL of ethyl acetate 3 times. The crude tannin was purified further with a Sephadex LH-20 column (1.5 cmˆ100 cm). The column was then eluted with 50% methanol to remove sugars, followed by elution with an acetone/water (70/30, v/v) mixture. The elution solution was freeze dried and stored at´20˝C for further use. The incubation was conducted using 1 mL of fresh/sterilized spore suspension of A. awamori incubated with 20 mL of the sterilized Czapek medium (121˝C, 30 min) containing 0.15 g of NaNO 3 , 0.02 g of K 2 HPO 4 , 0.01 g of KCl, 0.01 g of MgSO 4¨7 H 2 O, 0.2 mg of FeSO 4 and 3 g of sucrose for 2 days at 28˝C at 180 rpm rotation. Twelve milligrams of the purified condensed tannin were then added and cultured for another 4 days. The products were freeze dried and then extracted with acetone/water (70/30, v/v) before analysis. The experiments were conducted with triplicate biological repeats.

Measurements of Contents of Total Phenolics and Flavonoids
The content of total phenolics was determined according to the method of Quettier et al. [38]. In brief, samples (0.1 mL) were mixed with 5 mL of distilled water and 0.5 mL of Folin-Ciocalteu phenol reagent and incubated for 8 min at room temperature. Twenty percent Na 2 CO 3 (1.5 mL) was then added and heated in boiling water for 1 min. The absorbance was recorded at 760 nm using a spectrophotometer (Uico Shanghai Instrument Co., Ltd., Shanghai, China). Total phenolic content was expressed as milligrams of gallic acid equivalent (GAE) on a dry weight (DW) basis (mg GAE/g DW) from the calibration curve of the standard gallic acid. Total flavonoid content was determined by a colorimetric method using rutin as a reference compound [39]. Samples (1 mL) were mixed with 4 mL of distilled water and 0.5 mL of 5% sodium nitrite. After incubation of 6 min, 0.5 mL of 10% aluminum nitrate was added and then allowed to stand for another 5 min before 4 mL of 1 M NaOH were added. The absorbance at 510 nm was measured immediately against 60% ethanol as a blank. Total flavonoid content was expressed as rutin equivalent (RE) on a dry weight basis (mg RE/g DW). All of the tests were conducted in triplicate.

HPLC Analysis
Samples were analyzed with a Shimadzu LC-20 AT HPLC (Shimadzu Corporation, Kyoto, Japan) coupled with a Vydac C18 column (218 TP, 250 mmˆ4.6 mm, 5-µm particle size, Sigma-Aldrich, St. Louis, MO, USA) and an SPD-10A UV-VIS detector. Solvents A (0.1% trifluoroacetic acid) and B (methanol) were used as the mobile phases at a flow rate of 1 mL/min. The gradient elution was conducted by the method of Yang and Zhai [40]

DPPH Radical Scavenging Assay
The extracts of the Aspergillus-treated and non-Aspergillus-treated LPP were subjected to the assessment of DPPH radical scavenging activity [41]. The control was carried out with 60% ethanol instead of the tested sample, whilst methanol instead of DPPH was used as a blank. The DPPH radical scavenging activity of the tested sample was calculated as the following equation.
DPPH radical scavenging activity p%q " p1´a bsorbance of sample´absorbance of blank absorbance of control ąqˆ100 (1)

Measurements of Total Tannin and Mean Polymerization Degree
The total tannin content was measured with the Bate-Smith method [40]. The A. awamori-treated or non-A. awamori-treated condensed tannin liquid was dried under vacuum and re-dissolved into methanol before 3 mL of n-butyl alcohol-HCl (95/5, v/v) were added. After 40 min of reaction at 97˝C, the mixture was rapidly cooled with cold water. Methanol instead of the tested sample was employed as the blank. The purified condensed tannin with a purity of 92% was employed as the reference compound. Total tannin content was quantified with a standard curve (Y = 307.02X + 2.6701, R 2 = 0.9972), where Y and X were the concentration of the condensed tannin (µg/mL) and the optical absorbance at 550 nm, respectively.
The terminal residue unit of the condensed tannin was determined by the method previously described by Butler et al. [4]. In brief, 0.5 mL of samples were mixed with 3 mL of vanillic aldehyde-glacial acetic acid (4%, v/v) solution and 1.5 mL of 4% HCl, followed by reaction for 5 min at 20˝C. Methanol instead of sample was used as a blank. The absorbance at 500 nm was recorded with a spectrophotometer. The amount of terminal catechol was determined by a colorimetric method using catechol as a reference with the standard curve (Y = 315.42X´1.6001, R 2 = 0.9986), where Y and X were the concentration of the terminal unit (µg/mL) and the optical absorbance at 500 nm, respectively. The mean polymerization degree was calculated as the ratio of total tannin to the amount of terminal residue.

ESI-TOF-MS Analysis
To further understand the effect of incubation on the molecular weight of the condensed tannin, the A. awamori-treated or non-A. awamori-treated condensed tannin was subjected to ESI-TOF-MS analysis. Electrospray time-of-flight mass spectra (ESI-TOF-MS) (accurate mass) were measured in the positive-ion mode using an Agilent MSD-TOF mass spectrometer with a capillary voltage of 3000 V, nebulizer pressure of 40 psi, drying gas of 4 L/min and mass range of m/z 100-3500. Samples from three parallel incubations described in Section 3.4 were analyzed.

Phloroglucinolysis Analysis of Condensed Tannin
Condensed tannin is a kind of large molecular polyphenol composed of several kinds of flavan-3-ol, including epi/catechin, epi/afzelechin or their gallate derivants with the C4-C8 linkage (B-type) or the C4-C8 coupled with C2-O-C7 double linkage (A-type) [42,43]. The C4 position of the B-type linkage in the condensed tannin can be attacked with phloroglucinol to form a free terminal subunit and phloroglucinol adduct of extend subunits (A-type or B-type) ( Figure 6). The released terminal subunit and phloroglucinol adduct of extension subunits can be identified with HPLC-ESI-MS 2 . Briefly, the condensed tannin (5 g/L) was reacted for 20 min with a solution of 0.1 M HCl in MeOH, containing 50 g/L phloroglucinol and 10 g/L of ascorbic acid at 50˝C, and the reaction was stopped by the addition of 5 volumes of 40 mM aqueous sodium acetate [44].

ESI-TOF-MS Analysis
To further understand the effect of incubation on the molecular weight of the condensed tannin, the A. awamori-treated or non-A. awamori-treated condensed tannin was subjected to ESI-TOF-MS analysis. Electrospray time-of-flight mass spectra (ESI-TOF-MS) (accurate mass) were measured in the positive-ion mode using an Agilent MSD-TOF mass spectrometer with a capillary voltage of 3000 V, nebulizer pressure of 40 psi, drying gas of 4 L/min and mass range of m/z 100-3500. Samples from three parallel incubations described in Section 3.4 were analyzed.

Phloroglucinolysis Analysis of Condensed Tannin
Condensed tannin is a kind of large molecular polyphenol composed of several kinds of flavan-3ol, including epi/catechin, epi/afzelechin or their gallate derivants with the C4-C8 linkage (B-type) or the C4-C8 coupled with C2-O-C7 double linkage (A-type) [42,43]. The C4 position of the B-type linkage in the condensed tannin can be attacked with phloroglucinol to form a free terminal subunit and phloroglucinol adduct of extend subunits (A-type or B-type) ( Figure 6). The released terminal subunit and phloroglucinol adduct of extension subunits can be identified with HPLC-ESI-MS 2 . Briefly, the condensed tannin (5 g/L) was reacted for 20 min with a solution of 0.1 M HCl in MeOH, containing 50 g/L phloroglucinol and 10 g/L of ascorbic acid at 50 °C, and the reaction was stopped by the addition of 5 volumes of 40 mM aqueous sodium acetate [44]. The products were identified using an Agilent 1100 series HPLC system (Agilent Technologies, Waldbronn, Germany) coupled with a Vydac C18 column and a diode array detector (DAD) and an ion-trap mass spectrometer fitted with an ESI source (Bruker Daltonics HCT Ultra, Bremen, Germany). Solvents A (0.1% formic acid) and B (acetonitrile) were used as the mobile phase at a flow rate of 0.8 mL/min, with the following gradient elution program of 5% B for 0-10 min, 5%-20% B for 10-30 min, 40% B for 30-55 min and 100% B for 55-60 min. The temperature of the column was maintained at 25 °C. The products were identified using an Agilent 1100 series HPLC system (Agilent Technologies, Waldbronn, Germany) coupled with a Vydac C18 column and a diode array detector (DAD) and an ion-trap mass spectrometer fitted with an ESI source (Bruker Daltonics HCT Ultra, Bremen, Germany). Solvents A (0.1% formic acid) and B (acetonitrile) were used as the mobile phase at a flow rate of 0.8 mL/min, with the following gradient elution program of 5% B for 0-10 min, 5%-20% B for 10-30 min, 40% B for 30-55 min and 100% B for 55-60 min. The temperature of the column was maintained at 25˝C. The injection volume was 20 µL. The MS was operated in both positive and negative modes with Auto-MS n using a ramping of the collision energy. The operation condition was set as follows: capillary voltage of 4000 V and skimmer voltage of 30 V. The nebulizer pressure was 40 psi at a nitrogen flow rate of 9 L/min. The monitored mass range was from m/z 70-1200. Three parallel incubations described in Section 3.4 were used for phloroglucinolysis analysis of condensed tannin.

Statistical Analysis
Data are expressed as the means˘standard deviations (SD) and then were analyzed by OriginPro 8 (OriginLab Corporation, Northampton, MA, USA). One-way analysis of variance (ANOVA) and Tukey's multiple comparisons were carried out to test any significant differences between the means. Differences between means at the 5% level were considered significant.

Conclusions
In this study, the effects of A. awamori, A. sojae and A. oryzae incubations with LPP on polyphenol extraction recovery and DPPH radical scavenging activity of litchi pericarp were investigated. The study suggested that these incubations can increase significantly the extraction recovery of polyphenols from litchi pericarp, possibly because of the release of non-extractable condensed tannin. Furthermore, the products from the application of A. awamori possessed the highest antioxidant activity among them. It was found that A. awamori treatment can degrade B-type condensed tannin (condensed flavan-3-ol via the C4-C8 linkage) well, but had a low capacity to degrade the condensed tannin containing many A-type linkage subunits (C4-C8 coupled C2-O-C7 linkage). These results suggest that application of A. awamori can significantly improve the production of condensed tannin from litchi pericarp.