Probiotic Potential and Cholesterol-Lowering Capabilities of Bacterial Strains Isolated from Pericarpium Citri Reticulatae ‘Chachiensis’

Pericarpium Citri Reticulatae ‘Chachiensis’ (PCR-Chachiensis), the pericarps of Citri Reticulatae Blanco cv. Chachiensis, is a food condiment and traditional medicine in southeast and eastern Asia. Its rich and various bacterial community awaits exploration. The present study is the first report on probiotic screening and characterization of bacteria from PCR-Chachiensis. Based on 64 culturable bacterial isolates, 8 strains were screened out to have great survival in the simulated gastrointestinal stressful condition, being nonhemolytic and without biogenic amine formation. They were identified by 16S rRNA gene sequencing as two Bacillus, three Lactobacillus, and three strains from Bacillales. Their probiotic properties, cholesterol-lowering potential and carbohydrate utilization capability were further investigated. Though these eight strains all displayed distinct cholesterol removal potential, Bacillus licheniformis N17-02 showed both remarkable cholesterol removal capability and presence of bile salt hydrolase gene, as well as possessing most of the desirable probiotic attributes. Thus, it could be a good probiotic candidate with hypocholesterolemic potential. Bacillus megaterium N17-12 displayed the widest carbohydrate utilization profile and the strongest antimicrobial activity. Hence, it was promising to be used as a probiotic in a host and as a fermentation starter in fermented food or feed.


Introduction
Pericarpium Citri Reticulatae (in Chinese Chen Pi) is the dried and aged pericarps of Citrus reticulata Blanco and its cultivars. Other than being a food condiment used widely in cuisine and beverages for hundreds of years in southeast and eastern Asia, it is also a traditional medicine to cure chronic indigestion and respiratory diseases [1]. Extensive studies have been reported on its phytochemistry composition, especially phenolic composition [1]. Recently, bioactivities, such as antioxidant, antifungal and antiviral activities, were reported to boost its health benefits [2][3][4][5]. For example, the neuroprotective effects of the flavonoids and the antiviral activity of the polymethoxylated flavones [3,5]. Pericarpium Citri Reticulatae 'Chachiensis' (PCR-Chachiensis, in Chinese Guang Chen Pi), is the aged pericarps of Citri Reticulatae Blanco cv. Chachiensis and it has been proven by long-term practice as the premium Pericarpium Citri Reticulatae [1,2,[6][7][8]. Our previous study has revealed the central bacterial community in PCR-Chachiensis for the first time through amplicon sequencing, and identified Bacillus as the most dominant genus [6]. These special bacterial communities might contribute to the superior quality of PCR-Chachiensis.
Probiotics are defined as living microorganisms that confer various health benefits upon the host when ingested in adequate amounts [9]. Probiotics are gaining popularity worldwide and there is an increasing market for functional food and feed calls for novel

Hemolytic Test
The strains were streaked or spotted on agar plates containing sheep blood and incubated at 37 • C for 48 h [21]. Strains that had a green zone around the colony (α-hemolysis, partial hydrolysis), or formed a clear zone around the colony (β-hemolysis, complete hydrolysis) failed in the test. Only isolates that did not produce any zone around the colony were designated as no hemolysis.

Resistance To Artificial Gastric Juice and Intestinal Juice
The resistance of strains to gastric acid and intestinal juice was determined following the assay reported previously [22,23] with modifications. Artificial gastric juice contained 0.3% (w/v) pepsin from porcine gastric mucosa (Sigma Aldrich, St. Louis, MO, USA) with a Microorganisms 2021, 9,1224 3 of 14 pH of 2.5. Artificial intestinal juice was prepared by dissolving 0.3% (w/v) bile salt (Sigma Aldrich, St. Louis, MO, USA) and 1 mg/mL trypsin (Biofroxx, Einhausen, Germany) in sterile saline solution and adjusting the pH to 8.0. After overnight cultivation, the strains were precipitated and washed twice with phosphate buffer (PBS, pH = 7.4) and then resuspended in PBS (pH = 2.5 or pH = 8.0). Cell suspension at 1% (v/v) was injected into artificial gastric juice and incubated at 37 • C for 4 h or intestinal juice for 6 h respectively. The viable cells before and after incubation were determined by dilution plate counting.
Relative survival ratio (%) = CFU of viable cells survived/CFU of initial viable cells inoculated × 100

Biogenic Amine Formation
Formation of biogenic amines was tested using chromogenic medium as described previously [24]. Bacterial culture was inoculated in one of the four kinds of LB-based screening broth media (pH = 5.0) with 0.006% bromocresol purple: LB control, 0.5% yeast extract, 1% tryptone and 1% sodium chloride; LB-GL, control LB including 0.25% glycerol; LB-GLO, LB-GL including 0.01% ornithine; LB-GLH, LB-GL including 0.01% histidine. After 24 h incubation, the color, pH and absorbance at 590 nm of the supernatant were measured. Using this method, the generation of biogenic amines is indicated as a color change to purple in the precursor amino acid containing medium.

Auto-Aggregation and Hydrophobicity Assay
Auto-aggregation ability was evaluated according to the method described in a previous study [25] with modifications. The overnight culture was centrifuged, washed twice with PBS and then resuspended to OD 600 of 0.4 ± 0.05. Then, the OD 600 of upper suspension after incubation at 37 • C for 0, 2, 4, 6 and 24 h was measured.
Auto-aggregation (%) = (1 − A 2,4,6 or 24 h /A 0 h ) × 100 The measurement of cell surface hydrophobicity followed the method described previously [26] with modifications. The overnight culture was suspended in 0.1 M KNO 3 (pH 6.2) to 1 × 10 8 cells ml −1 and absorbance measured at 600 nm (A 0 ) with a Spectrophotometer UV2300. Then, 1 mL dichloromethane and ethyl acetate were added into 3 mL cell suspension, respectively, and mixed with vortex for 5 min. The OD 600 of aqueous phase was measured after standing for 15 min (A 1 ).

Antimicrobial Activity and Co-Aggregation
The antimicrobial activity of the strains was determined using the microplate assay as described previously [27], against Escherichia coli (CMCC 44102), Salmonella paratyphi (CMCC 50094), Staphylococcus aureus (CMCC 26003) and Bacillus subtilis (CMCC 63501) purchased from Guangdong Institute for Drug Control, China. Supernatants of overnight cultures were evaluated in antimicrobial assay in their initial pH or neutralized to pH 6.5. The determination of co-aggregation between isolates and indicator bacteria strains followed the method as described previously [25].

Antibiotic Susceptibility
The selected strains were evaluated for antibiotic susceptibility by disk method [28]. The inhibition zone diameters were measured with a vernier caliper and compared with the criteria mentioned in this reference.
Bile salt hydrolase (BSH) activity was assessed using the method described previously [29,30] with modification. Sodium taurodeoxycholic acid (TDCA) and sodium glycodeoxycholic acid (GDCA) at 0.5% (w/v) were used as bile salt substrates. The colonies displaying white precipitates were scored as BSH activity.
To amplify bsh gene, degenerate primers were designed by retrieving the corresponding amino acid sequence of BSH from similar strains in NCBI (https://www.ncbi.nlm.nih. gov/) (accessed on 9 September 2020). The degenerate primers used were shown in Table 1. Touchdown PCR was applied in the PCR instrument (Eastwin Scientific Equipments Inc., Suzhou, China) and the PCR amplicons were sequenced. Amino acid sequences of BSHs were aligned through Clustal Omega (http://www.clustal.org/omega/) (accessed on 14 October 2020) [31]. Table 1. Primers used to screen bsh gene.

Cholesterol Removal Ability
The cholesterol removal ability was evaluated according to the method described previously [30] with modification. The overnight culture was inoculated at 1 mL/100 mL in LB or MRS medium containing cholesterol at a final concentration of 100 µg/mL. After incubation at 37 • C for 6, 12, 18 and 24 h, the cholesterol left in the supernatant was measured spectrophotometrically via the o-phthalaldehyde method and calculated according to the standard curve. The GDCA at 2.8 mM and TDCA at 1.2 mM were used as bile when indicated.

Carbohydrate Utilization Capability
Utilization of seven sugars and two sugar alcohols, including D-glucose, D-xylose, lactose, sucrose, cellobiose, stachyose, D-raffinose, sorbitol and mannitol, were evaluated according to the method described previously [32] with modification. The carbohydrates were prepared into a 10% solution respectively and sterilized through filtration by 0.22 µm Millex ® -GP (Merck Millipore Ltd., Cork, Ireland). They were used as the main carbon source in the basic MRS (without glucose and meat extract) or LB (without tryptone and yeast extract) medium. The 1% (v/v) cell suspension (10 8 cells mL −1 ) was inoculated into medium containing 2% (w/v) carbohydrate solution. The optical densities at 600 nm (OD 600 ) were recorded and compared with negative control after incubation at 37 • C for 48 h.

Statistical Analysis
Data were expressed as means ± standard error (SE) of at least three replicates. Analysis of variance (ANOVA) and significance of differences (p < 0.05) between the means of parameters in the results were calculated using SPSS 22.0 software (SPSS Inc., Chicago, IL, USA).

Identification of Culturable Bacterial Strains in PCR-Chachiensis
A total of 64 bacterial strains were isolated from PCR-Chachiensis and their identities were determined based on the phenotypic and genotypic characterization ( Figure 1, Table S1). The 16S rDNA sequencing assigned 53 strains in Bacillaceae, among which 49 strains belonging to the genus Bacillus and the rest to different genera under Bacillaceae, such as Lysinibacillus, Terribacillus, Virgibacillus and Quasibacillus. Several strains from genus Lactobacillus and Paenibacillus were also confirmed, which might open up new opportunities for probiotics. ties were determined based on the phenotypic and genotypic characterization ( Figure 1, Table S1). The 16S rDNA sequencing assigned 53 strains in Bacillaceae, among which 49 strains belonging to the genus Bacillus and the rest to different genera under Bacillaceae, such as Lysinibacillus, Terribacillus, Virgibacillus and Quasibacillus. Several strains from genus Lactobacillus and Paenibacillus were also confirmed, which might open up new opportunities for probiotics.

Hemolytic Activity Test
As displayed in Figure 1, some of the closely related reference Bacillus strains such as B. coagulans, B. licheniformis, B. subtilis and B. megaterium are currently used as probiotics in clinical trials or commercial products [12], while strains such as Virgibacillus halophilus, Figure 1. Phylogenetic tree analysis and primary screening of 65 strains isolated from PCR-Chachiensis. The results of hemolytic, gastrointestinal tolerance and the production of amines were respectively represented by symbols from the inside to the outside as square, circle and star. A grey symbol indicates failure and a red one indicates passing the assay.

Hemolytic Activity Test
As displayed in Figure 1, some of the closely related reference Bacillus strains such as B. coagulans, B. licheniformis, B. subtilis and B. megaterium are currently used as probiotics in clinical trials or commercial products [12], while strains such as Virgibacillus halophilus, Paenibacillus chibensis and B. ginsengihumi have hardly been mentioned. Though Lactobacillus strains such as L. plantarum and L. rhamnosus have been widely studied as probiotics [33,34], the probiotic potential of L. senioris and L. curieae identified here have rarely been reported. Therefore, the hemolytic activity assay was conducted firstly to ensure the safety of potential probiotic strains. Isolates that could cause partial or complete lysis of red blood cells were excluded. Only isolates that did not produce any zone around the colony were designated as no hemolysis. A total of 22 strains, 12 from Bacillus, were screened out to pass the hemolytic test and subjected to the following assay ( Figure 1).

Determination of Gastrointestinal Survival and Biogenic Amine Formation
Survival in a gastrointestinal environment is a prerequisite for oral probiotic formulations to colonize the intestinal tract. Tolerance to artificial gastric juice and intestinal Microorganisms 2021, 9,1224 6 of 14 juice were tested among strains without hemolytic activity. A total of 18 out of 22 strains evaluated could survive through both gastric and intestinal juice ( Figure 1).
The active metabolism of amino acids, usually decarboxylation in microorganisms, might result in high levels of biogenic amines, which would have negative effects on vasoactivity and psychoactivity, or as the precursors of carcinogenic nitrosamines [35]. Thus, biogenic amine formation is a very important evaluation index for the safety of probiotics. The biogenic amine formation by the isolates was determined using a screening assay for amino acid decarboxylation from ornithine and histidine. Ten isolates having strong biogenic amine formation were excluded through this assay. Representative results of strains without biogenic amine formation are displayed in Table 2. red blood cells were excluded. Only isolates that did not produce any zone around the colony were designated as no hemolysis. A total of 22 strains, 12 from Bacillus, were screened out to pass the hemolytic test and subjected to the following assay ( Figure 1).

Determination of Gastrointestinal Survival and Biogenic Amine Formation
Survival in a gastrointestinal environment is a prerequisite for oral probiotic for mulations to colonize the intestinal tract. Tolerance to artificial gastric juice and intestina juice were tested among strains without hemolytic activity. A total of 18 out of 22 strains evaluated could survive through both gastric and intestinal juice ( Figure 1).
The active metabolism of amino acids, usually decarboxylation in microorganisms might result in high levels of biogenic amines, which would have negative effects on vasoactivity and psychoactivity, or as the precursors of carcinogenic nitrosamines [35] Thus, biogenic amine formation is a very important evaluation index for the safety o probiotics. The biogenic amine formation by the isolates was determined using a screening assay for amino acid decarboxylation from ornithine and histidine. Ten isolates having strong biogenic amine formation were excluded through this assay. Representa tive results of strains without biogenic amine formation are displayed in Table 2. red blood cells were excluded. Only isolates that did not produce any zone around the colony were designated as no hemolysis. A total of 22 strains, 12 from Bacillus, were screened out to pass the hemolytic test and subjected to the following assay ( Figure 1).

Determination of Gastrointestinal Survival and Biogenic Amine Formation
Survival in a gastrointestinal environment is a prerequisite for oral probiotic formulations to colonize the intestinal tract. Tolerance to artificial gastric juice and intestinal juice were tested among strains without hemolytic activity. A total of 18 out of 22 strains evaluated could survive through both gastric and intestinal juice ( Figure 1).
The active metabolism of amino acids, usually decarboxylation in microorganisms might result in high levels of biogenic amines, which would have negative effects on vasoactivity and psychoactivity, or as the precursors of carcinogenic nitrosamines [35] Thus, biogenic amine formation is a very important evaluation index for the safety of probiotics. The biogenic amine formation by the isolates was determined using a screening assay for amino acid decarboxylation from ornithine and histidine. Ten isolates having strong biogenic amine formation were excluded through this assay. Representative results of strains without biogenic amine formation are displayed in Table 2. colony were designated as no hemolysis. A total of 22 strains, 12 from Bacillus, were screened out to pass the hemolytic test and subjected to the following assay ( Figure 1).

Determination of Gastrointestinal Survival and Biogenic Amine Formation
Survival in a gastrointestinal environment is a prerequisite for oral probiotic formulations to colonize the intestinal tract. Tolerance to artificial gastric juice and intestinal juice were tested among strains without hemolytic activity. A total of 18 out of 22 strains evaluated could survive through both gastric and intestinal juice ( Figure 1).
The active metabolism of amino acids, usually decarboxylation in microorganisms, might result in high levels of biogenic amines, which would have negative effects on vasoactivity and psychoactivity, or as the precursors of carcinogenic nitrosamines [35]. Thus, biogenic amine formation is a very important evaluation index for the safety of probiotics. The biogenic amine formation by the isolates was determined using a screening assay for amino acid decarboxylation from ornithine and histidine. Ten isolates having strong biogenic amine formation were excluded through this assay. Representative results of strains without biogenic amine formation are displayed in Table 2. colony were designated as no hemolysis. A total of 22 strains, 12 from Bacillus, were screened out to pass the hemolytic test and subjected to the following assay ( Figure 1).

Determination of Gastrointestinal Survival and Biogenic Amine Formation
Survival in a gastrointestinal environment is a prerequisite for oral probiotic formulations to colonize the intestinal tract. Tolerance to artificial gastric juice and intestinal juice were tested among strains without hemolytic activity. A total of 18 out of 22 strains evaluated could survive through both gastric and intestinal juice (Figure 1).
The active metabolism of amino acids, usually decarboxylation in microorganisms, might result in high levels of biogenic amines, which would have negative effects on vasoactivity and psychoactivity, or as the precursors of carcinogenic nitrosamines [35]. Thus, biogenic amine formation is a very important evaluation index for the safety of probiotics. The biogenic amine formation by the isolates was determined using a screening assay for amino acid decarboxylation from ornithine and histidine. Ten isolates having strong biogenic amine formation were excluded through this assay. Representative results of strains without biogenic amine formation are displayed in Table 2.  [33,34], the probiotic potential of L. senioris and L. curieae identified here have rarely bee reported. Therefore, the hemolytic activity assay was conducted firstly to ensure th safety of potential probiotic strains. Isolates that could cause partial or complete lysis o red blood cells were excluded. Only isolates that did not produce any zone around th colony were designated as no hemolysis. A total of 22 strains, 12 from Bacillus, wer screened out to pass the hemolytic test and subjected to the following assay ( Figure 1).

Determination of Gastrointestinal Survival and Biogenic Amine Formation
Survival in a gastrointestinal environment is a prerequisite for oral probiotic fo mulations to colonize the intestinal tract. Tolerance to artificial gastric juice and intestin juice were tested among strains without hemolytic activity. A total of 18 out of 22 strain evaluated could survive through both gastric and intestinal juice ( Figure 1).
The active metabolism of amino acids, usually decarboxylation in microorganism might result in high levels of biogenic amines, which would have negative effects o vasoactivity and psychoactivity, or as the precursors of carcinogenic nitrosamines [35 Thus, biogenic amine formation is a very important evaluation index for the safety o probiotics. The biogenic amine formation by the isolates was determined using screening assay for amino acid decarboxylation from ornithine and histidine. Ten isolate having strong biogenic amine formation were excluded through this assay. Represent tive results of strains without biogenic amine formation are displayed in Table 2. Thus far, eight strains were screened out after the primary safety assessment an gastrointestinal tolerance evaluation. These strains were retained for subsequent chara terization of probiotic properties. Three of them were Lactobacillus (N15-22, X16-6 X16-69), similar to L. senioris and L. curieae. The other five strains were Bacillales, amon Overall, all of these eight strains had reasonable chance of survival in the simulated gastrointestinal environment, while Y11-38 and Y13-51 showed the most prominent adaptability (Table 3). Relatively higher survival rates were found in Bacillus strains than in Lactobacillus strains. The survival rates of Bacillus strains were in the range of 67.18-96.89% and rates of Lactobacillus strains were in the range of 3.60-25.00% after exposure to artificial gastric juice for 4 h. Similarly, in artificial intestinal juice they were 45.18-48.06% for Bacillus strains and 27.36-43.48% for Lactobacillus strains. This observation was consistent with previous reports about the greater viability of Bacillus strains than Lactobacillus strains when exposed to simulated gastrointestinal conditions or tea and coffee brewing [16,17,36].

Auto-Aggregation and Cell Surface Hydrophobicity
Probiotic candidates should be able to attach onto the epithelium lining of the ileum in the host before they could provide health benefits, thus their adhesion ability was assessed through auto-aggregation and cell surface hydrophobicity assay. High auto-aggregation is correlated with effective adhesion and subsequent colonization in the gastrointestinal tract. The auto-aggregation of these eight strains increased with the incubation time, reaching a range of 26.12-94.97% at 6 h and 52.53-95.56% at 24 h, respectively (Table 4). Among them, N15-22 and N17-02 had the highest auto-aggregation (95.56% and 93.69%) at 24 h. However, given that chyme spends on average 4-8 h in the ileum [18], B. licheniformis N17-02 was considered the best one due to the fact that its auto-aggregation rapidly increased in the first 6 h. Hydrophobicity reveals the relative tendency of a substance to prefer nonaqueous rather than aqueous environments. A high cell surface hydrophobicity of a probiotic candidate indicates its probability to attach onto the epithelial lining of the intestine and resist the quick expelling from intestines. Here, the adhesion ability to hydrocarbons dichloromethane and ethyl-acetate were measured (Table 4). Interestingly, the hydrophobicity measurements in three Lactobacillus strains were higher than that of strains in Bacillales for both dichloromethane and ethyl-acetate, as high as 90.76-98.05% and 90.59-97.83%, respectively. Compared with the hydrophobicity reported previously, such as Bacillus strains to ethyl-acetate [21,29] and Lactobacillus isolates to dichloromethane [37], the hydrophobicity measurements of the strains evaluated here were comparable or even higher.
In general, based on the auto-aggregation and hydrophobicity, these eight strains have good adhesion ability. Probiotics that aggregate and accumulate in sufficient quantities to form an immune barrier could protect the gut from pathogens, maintain the balance and stability of intestinal flora and perform the other functions of probiotics [38].

Antibacterial Activity and Co-Aggregation
The antibacterial activity of isolates was tested against enteric bacterial pathogens, including Staphylococcus aureus, Salmonella paratyphi, Escherichia coli and Bacillus subtilis (Table 5). For Bacillales strains, significant inhibition was observed only in N17-02 against S. aureus and N17-12 against S. paratyphi and E. coli. The original supernatants of Lactobacillus strains culture had significant inhibitory effects against most pathogens tested except N15-22 against E. coli, but the antibacterial activity decreased after adjusting the supernatant to neutral. Thus, acid production might be an essential component of antibacterial activity in Lactobacillus strains, or acidic conditions might be beneficial for the function of their bacteriostatic substances. Similarly, organic acids including lactic acid were reported to be responsible for the antagonistic effect of several lactic acid bacteria derived from fermented food [39]. Table 5. Antibacterial activity and co-aggregation ability of probiotic strains against indicator strains. The plus or minus sign indicates the difference in antibacterial activity among probiotics strains. -, no antibacterial activity; +, antibacterial activity but not significant; ++, significant antibacterial activity as p < 0.05; +++, significant antibacterial activity as p < 0.01. B Co-aggregation is expressed as percentage. C The plus or minus sign before and after slash indicate antibacterial activity using original supernatant in its initial acidic pH and supernatant neutralized to pH 6.5. Different lowercase superscripts ( a, b, c, d, e, f ) represent significantly different values (p < 0.05) in the same column. Values are expressed as mean ± SE (n = 3).

Staphylococcus aureus
From the point of view of co-aggregation, these eight strains had co-aggregation at 46.67-69.18%, 50.98-67.49%, 48.00-59.36% and 70.78-82.10% to S. aureus, S. paratyphi, E. coli and B. subtilis, respectively (Table 5). These data implied that these isolates had good chances to co-aggregate with pathogens to interfere with their retention and colonization in gastrointestinal tract. The highest co-aggregation with S. aureus and B. subtilis was observed in X16-69 and N17-02, respectively. The highest co-aggregation with S. paratyphi and E. coli was found in N17-12, together with its significant antibacterial activity against these two pathogens, thus B. megaterium N17-12 was suggested as a good probiotic candidate from the point of view of the antibacterial potential. Three B. megaterium strains were isolated recently from stingless bee honey collected across Malaysia and subjected to probiotic screening, but they were found to have no inhibition effect against six pathogenic bacteria, including Salmonella thyphimurium and E. coli [40]. Thus, the probiotic property of B. megaterium was strain specific.

Antibiotic Susceptibility
Given the possibility of transfer of antibiotic resistance genes from probiotic bacteria to gut pathogens, the antibiotic susceptibility was evaluated in these eight strains. According to their classification and mechanisms of action [41], different antibiotics such as β-lactams (penicillin-G, ampicillin and cephalothin), macrolides (erythromycin), tetracyclines, aminoglycosides (gentamicin), glycopeptides (vancomycin) and chloramphenicol were chosen. Results indicated that each isolate was sensitive to at least three or more antibiotics (Table 6), which verified their safe utilization. Synthetically, Y13-51 showed the highest vulnerability to antibiotics tested. Most Bacillales strains were resistant to penicillin-G, probably due to the narrow antibacterial spectrum of penicillin-G. The Lacto-bacillus strains N15-22 and X16-68 were resistant to vancomycin and gentamicin, thus they might be applied to reduce the diarrhea caused by antibiotic damage to intestinal flora [42]. It needs to be further evaluated whether these antibiotic resistances were transferable before application. At this point, eight isolates had met the selection criteria, i.e., gastrointestinal tract stress tolerance, adhesion ability, antimicrobial activity and primary safety assessment, to be probiotic candidates. Then, the cholesterol-lowering capabilities and carbon source utilization were further investigated to explore their functional properties.

Cholesterol-Lowering Potential
Attention was first paid to the bile salt hydrolase (BSH), choloylglycine hydrolase (EC3.5.1.24), which is suggested to contribute to the detoxification of bile acid (BA), and is associated with the therapeutic effect of decreasing host cholesterol [19,43,44]. Unfortunately, using TDCA and GDCA as BA substrates, the positive BSH activity as a white precipitation zone around the colonies was not observed in our experiment. Since non-concordance between BSH phenotypic assay and presence of bsh gene was reported recently in Enterococcus faecium isolated from rhizosphere [30], we further searched for the bsh gene in these eight isolates. According to the bsh genes in similar strains as reference, touchdown PCR successfully retrieved six bsh genes from five isolates, including N17-02, N17-12, Y11-38, X16-66 and N15-22. In particular, two different bsh genes were identified in L. senioris N15-22 (Figure 2). High similarity was observed between the identified BSHs and the reference BSHs ( Figure 2, Figure S2), which implied their functionality. A latest report in PNAS emphasized the substrate specificity of BSHs from Lactobacillus, which governs bacterial fitness and host colonization [45]. This might help explain the negative result in BSH activity assay, since only TDCA and GDCA were tested as substrates. Further analysis is needed to investigate whether these putative enzymes could act as functional BSHs.
Then, the direct cholesterol removal capability, including cholesterol assimilation, absorption and adsorption, were evaluated in these eight strains. All of them displayed distinct cholesterol removal potential, and the removal rate ranged from 11.85% to 93.94% within 24 h ( Figure 3A). The highest cholesterol removal rates were found over 90% at 6 h in B. licheniformis N17-02 and 18 h in P. chibensis Y13-51, respectively. Compared with three Lactobacillus strains, the removal rates were relatively higher in five isolates from Bacillales, ranging from 27.18% to 93.94%, which were higher than the removal rate 12.82-70.89% reported previously in Bacillus strains isolated from fermented vegetables [46]. To test whether bile salt could boost the relatively lower removal rate in Lactobacillus strains N15-22, X16-68 and X16-69, GDCA and TDCA were added. Significant increase of removal rate was observed at 18 h in all three strains, to a maximum of 69.48% in L. curieae X16-68 ( Figure 3B). The addition of bile salts might affect the cell surface structure to varying degrees, thus promoting cholesterol removal rate [19]. identified in L. senioris N15-22 (Figure 2). High similarity was observed between the identified BSHs and the reference BSHs (Figure 2, Figure S2), which implied their functionality. A latest report in PNAS emphasized the substrate specificity of BSHs from Lactobacillus, which governs bacterial fitness and host colonization [45]. This might help explain the negative result in BSH activity assay, since only TDCA and GDCA were tested as substrates. Further analysis is needed to investigate whether these putative enzymes could act as functional BSHs.  [45]. The identical amino acids are indicated by asterisks; the conservative and semi conservative amino acids are indicated by two dots and one dot, respectively. N in the LTN-conserved motif and R in the RF-conserved motif are the previously described conserved active-site residues.
Two possible mechanisms have been proposed regarding the hypocholesterolemia effect of probiotics: one is the direct binding or assimilation of cholesterol by probiotics and the other one is bile salt deconjugation catalyzed by BSH [19]. Intestinal bacterial BSHs cleave glycine or taurine from conjugated BAs, an essential upstream step for the production of deconjugated and secondary BAs. Deconjugated BAs are less soluble and resorbable than the conjugated ones in the intestine, thus rendering them easier to be excreted in feces and subsequently more conjugated BA should be synthesized de novo from cholesterol, thereby reducing the cholesterol concentration [19,47]. Another consequence is the lower emulsifying ability of deconjugated bile salts compared to conjugated ones, which may result in lower lipid digestion and decreased absorption of cholesterol, fatty acids and monoglycerides in the intestine [19,44,48]. The obvious cholesterol removal ability and the presence of bsh genes in these isolates here suggested that they could be good probiotic candidates with hypocholesterolemia effect. Especially, B. licheniformis N17-02 showed both remarkable cholesterol removal capability and presence of bsh gene. 93.94% within 24 h ( Figure 3A). The highest cholesterol removal rates were found over 90% at 6 h in B. licheniformis N17-02 and 18 h in P. chibensis Y13-51, respectively. Compared with three Lactobacillus strains, the removal rates were relatively higher in five isolates from Bacillales, ranging from 27.18% to 93.94%, which were higher than the removal rate 12.82-70.89% reported previously in Bacillus strains isolated from fermented vegetables [46]. To test whether bile salt could boost the relatively lower removal rate in Lactobacillus strains N15-22, X16-68 and X16-69, GDCA and TDCA were added. Significant increase of removal rate was observed at 18 h in all three strains, to a maximum of 69.48% in L. curieae X16-68 ( Figure 3B). The addition of bile salts might affect the cell surface structure to varying degrees, thus promoting cholesterol removal rate [19].  BSH was confirmed to be the key factor affecting the hypocholesterolemia activity of Lactobacillus-fermented milk in hamsters [43] and Lactobacillus-yoghurt formulation in hypercholesterolemic adults [49]. Nevertheless, over-extensive secondary BA might be associated with diseases such as steatosis and colorectal carcinoma [19,50,51]. Therefore, more in vivo experiments are needed to support refined applications.

Carbohydrate Utilization Capability
The carbohydrate utilization profiles of these eight strains were investigated against two monosaccharides, three disaccharides, one trisaccharide, one tetrasaccharide and two sugar alcohols (Table 7). All eight strains could make use of at least five carbon sources. In particular, B. megaterium N17-12 showed significant growth on all the carbohydrate sources tested, including D-glucose, D-xylose, lactose, sucrose, cellobiose, stachyose, D-raffinose, sorbitol and mannitol. Such a wide carbohydrate utilization profile might suggest the growth advantage among GIT microbiota in host, where the competition in nutrition was fierce. Interestingly, N17-12 also displayed the strongest inhibitory effect against S. paratyphi and E. coli (Table 5), thus together confirming its great potential as probiotics. Other than being good as a probiotic to function in a host, the wide carbohydrate utilization profile also suggested its potential as a fermentation starter in fermented food or feed. For example, dough fermentation with Lactobacillus was investigated recently to improve the nutritional quality of foodstuff [52,53]. The application of these eight strains in the fermentation of food or feed will be investigated in the future.

Conclusions
In this study, probiotics screening and characterization of bacteria from PCR-Chachiensis was reported for the first time and results demonstrated that PCR-Chachiensis was a reservoir of potential probiotics. Our results indicated that eight isolates showed great survival in the simulated GIT stressful conditions, with nonhemolytic and no biogenic amine formation. Though these eight strains all displayed distinct cholesterol removal potential, B. licheniformis N17-02 showed both remarkable cholesterol removal capability and presence of the bsh gene, as well as possessing most of the desirable probiotic attributes. Thus, it could be a good probiotic candidate with hypocholesterolemic potential. B. megaterium N17-12 displayed the widest carbohydrate utilization profile and the strongest antimicrobial activity. Hence, it was promising to be used as a probiotic in host and as a fermentation starter in fermented food or feed. Further in vitro and in vivo analysis should be performed so that these isolates could be used for human or animal and food or feed applications.

Conflicts of Interest:
The authors declare no conflict of interest.