Effects of zinc-bearing palygorskite on rumen fermentation in vitro

Article information

Asian-Australas J Anim Sci. 2019;32(1):63-71

Publication date (electronic) : 2018 April 19

doi : https://doi.org/10.5713/ajas.17.0920

Mengjiao Chen¹, Yumeng Xi², Lin Zhang¹, Hanfang Zeng¹, Yeqing Li¹, Zhaoyu Han^1,

¹Institute of Dairy Science, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095,China

²Animal Husbandry Institute, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China

^*Corresponding Author: Zhaoyu Han, Tel: +86-0-25-84395314, Fax: +86-0-25-84395314, E-mail: zyhan6708@njau.edu.cn

Received 2017 December 21; Revised 2018 February 6; Accepted 2018 April 16.

Abstract

INTRODUCTION

Palygorskite (Pal) is a common clay mineral, which has a large surface area, a moderate layer charge, ion-exchange and adsorption ability, and rheological and catalytic properties with its special micropores and channels, fine particle size and fibrous habit [1] and these characters make it be applicable for use in many industries as well as animal nutrition [2]. Palygorskite can act as an adsorbent for toxins, bacteria and even viruses in the intestine [3], and as a protective coating for the stomach and intestines. Zaid et al [4] found that palygorskite was effective in the treatment of mild-to-moderate acute diarrhea in humans as an additional safe agent. Recently, a study reported that palygorskite was beneficial to intestinal integrity, which improved growth performance in weaned piglets [5].

In clay mineral, as the carrier, load some metal ions, such as Ag⁺, Cu²⁺, Zn²⁺ preparation of inorganic antibacterial agent has good antibacterial properties. Zinc has many physiological functions, not only is an essential trace mineral which is required for growth, enzyme structure, and function for poultry [6], but also can regulate microbial activity [7]. Zinc-bearing clinoptilolite could act as an antibacterial agent against Salmonella, inhibiting Salmonella growth and improving the gut health [8]. Additionally, Zn bearing zeolite and montmorillonite have been synthesized based on their high specific area and adsorption capacity [9]. It has been demonstrated that supplementation of these Zn bearing nonmetallic minerals can promote growth performance, improve intestinal morphology, inhibit the growth of pathogenic bacteria and enhance intestinal antioxidant capacity [9,10]. Moreover, they could be replaced antibiotics widely used in poultry production due to their antimicrobial ability.

However, aside from its being a potential antibiotic in poultry, little was known about the application of zinc-bearing palygorskite (Zn-Pal) in dairy cattle. In this study, Pal was used to prepare Zn-Pal through the ion-exchange method and evaluated the bioavailability of Zn-Pal as a substitute of antibiotic for dairy cattle with technology of in-vitro-rumen fermentation.

MATERIALS AND METHODS

Zn-Pal, experimental design, and in vitro fermentation

Preparation of Zn-Pal

Palygorskite was kindly provided by Jiangsu Sinitic Biotech Co., Ltd. (Xuyi, Jiangsu, China). The chemical composition of Pal clay mineral is SiO₂ 53.73%, Al₂O₃ 10.90%, MgO 6.81%, CaO 3.08%, K₂O 2.00%, and Fe₂O₃ 7.84% (Table 1). Zn-Pal was prepared according to the method described by Yan et al [11]. In detail, palygorskite was first calcinated at around 300°C for 3 h in a muffle oven. After cooling down, palygorskite was mixed with ZnCl₂ (ZnCl₂≥98.0%; 4:1, wt/wt) purchased from Nanjing Chemical Reagent Co., Ltd. (Nanjing, Jiangsu, China) in a stainless steel blade grinder. The mixture was subsequently calcinated at 300°C for 3 h in a muffle oven. After cooling to room temperature, the mixture was washed repeatedly by deionized water until there was no white deposition generated in the washed solution when swigged with 0.1 mol/L AgNO₃ solution. Finally, the washed mixture was collected and dried at around 105°C for 2 h in an air oven, and then ground through a 200-mesh sieve after cooling down. The amount of Zn adsorbed by palygorskite was 24.5 mg/g with inductively coupled plasma mass spectrometry (ICP-MS, Optima 2100 DV, Perkin Elmer, Waltham, MA, USA) and according to the method described by Yan et al [11].

Table 1

The chemical composition of the palygorskites

Characterization of Zn-Pal

The main chemical compositions of Pal and Zn-Pal were determined by a Minipal 4X-ray fluorescence spectrometer (PAN, Almelo, Netherlands). X-ray diffraction (XRD) patterns were collected on an X’pert PRO X-ray power diffractometer, which equipped with a Cu-Kα radiation source (40 kV, 40 mA) from 3° to 80° (2θ) at a scanning step time of 15.2 s, with a step interval about 0.017°, divergence slit of 0.5°. The physico-chemical properties of Pal and Zn-Pal were shown in Table 2. Zeta potential of Pal and Zn-Pal were measured by a Malvern Zetasizer Nano system (Malvern Instruments, Malvern, UK) at 25°C, using a folded capillary cell. Before measurements, a sample of 0.50 g of obtained palygorskite was fully dispersed in 100 mL of distilled water under high-speed stirring at 11,000 rpm for 20 min. The specific surface area is determined by the Brunauer–Emmett–Teller (BET) method. Determinations of cation-exchange capacity and ethylene blue absorption were performed according to the method described by Qiao et al [12].

Table 2

Physico-chemical properties of the palygorskites

Experimental design

The substrate used was a common total mixed ration diet (with a 50:50 forage: concentrate diet, 54.6% dry matter, 17.15% crude protein, and 34.72% neutral detergent fiber, which was dried at 65°C for 48 h and broken up by passing it through a 1-mm screen. The composition and nutrient content of the basal diet are presented in Table 3.

Table 3

Composition and nutrient levels of basal diet in dairy cows after parturition (DM basis) %

Experiments were conducted to measure in vitro gas production (GP) characteristics of Zn-Pal. Inclusive levels of Zn-Pal were 0% (Control, n = 18), 0.2% (Treatment I, n = 18), 0.4% (Treatment II, n = 18), 0.6% (Treatment III, n = 18), 0.8% (Treatment IV, n = 18) in vitro incubation fluid, respectively. The Zn-Pal was mixed with the substrate before the commencement of the experiment. The pressure in the bottle was recorded at 3, 6, 9, 12, 18, 24, 36, 48, 60, and 72 h during the processes of in vitro fermentation. At 0, 6, 12, 24, 48, and 72 h, fluid was sampled to determine pH, NH₃-N, volatile fatty acid (VFA), microbial protein yield (MCP), and lipopolysaccharide (LPS).

Substrate, inoculum and incubation

All animals involved in this study were cared for according to the principles of Nanjing Agricultural University Animal Care and Use Committee. Rumen fluid was collected from 3 healthy dairy cows (650 kg of mean body weight), which were killed after a 7-day adaptation to the diet. Ruminal fluid was collected from different locations of rumen, and then mixed and strained through four layers of cheesecloth into a pre-warmed thermos flask. The 100 mL of rumen fluid-buffer mixture and rumen fluid in the ratio of 4 to 1, was dispensed anaerobically into bottles containing 1 g of total mixed ration and additives 0%, 0.2%, 0.4%, 0.6%, 0.8% Zn-Pal. The composition and dosage of the rumen fluid-buffer mixture are performed according to the method described by Theodorou et al [13]. The serum bottles were filled with O₂-free CO₂ gas, and then capped with a rubber stopper. The bottles were kept in an incubator (JSGI-250T, JSR, Gongju, Korea) at 39°C.

Measurement of in vitro fermentation parameters: During the incubation, the GP kinetics were recorded at 3, 6, 9, 12, 18, 24, 36, 48, 60, and 72 h. Cumulative GP data were fitted to the model of McDonald [14] as follows:

Y=A (1-e-c (t-L))

Where Y is the volume of GP (mL per 100 mg DM) at time t, A is GP from soluble and insoluble fraction, c is the rate of GP, L the lag time (h) and t is the incubation time (h).

After incubation at 39°C for 0, 6, 12, 24, 48, 72 h, fluid was sampled to determine pH, NH₃-N, VFA, MCP, and LPS. The pH value of in vitro fermentation liquid was determined using a pH meter (Model PHS-3C, Shanghai Precision & Scientific Instrument Co., LTD, Shanghai, China). NH₃-N content was determined by using a spectrophotometer (8500II, Thermo Electron Corporation, Waltham, MA, USA). MCP content was determined based on Lowry’s assay, with modifications described in Makkar [15], and bovine serum albumin was used as a standard. The levels of LPS were measured as described by Emmanuel et al [16] using the Limulus amoebocyte lysate assay (Xiamen Houshiji, Ltd., Xiamen, China). To determine VFAs, 1 mL of fermentation medium was placed in a centrifuge tube, mixed uniformly with 0.2 mL of 25% metaphosphoric acid using crotonic acid as an internal standard, and then centrifuged at 12,000×g for 10 min. The supernatant was decanted into another test tube, capped, and stored in a refrigerator at 4°C until being analyzed with gas chromatography (GC-14B; Shimadzu, Kyoto, Japan). Subsamples were injected into a 30 m×0.32 mm×0.25 μm capillary. The temperatures of the detector, column and vaporization were 220°C, 130°C, and 180°C, respectively. Nitrogen was used as a carrier.

RESULTS

Characterization of Zn-Pal

The X-ray diffraction patterns of the Pal and Zn-Pal samples are shown in Figure 1. The palygorskite with the characteristic reflections appeared at 2θ = 8.41° (d = 1.0503 nm, 110 crystal plane), 2θ = 13.72° (d = 0.6453 nm, 200 crystal plane), 2θ = 16.37° (d = 0.5412 nm, 130 crystal plane), and 2θ = 19.81° (d = 0.4482 nm, 400 crystal plane), respectively. And the Zn-Pal with the characteristic reflections appeared at 2θ = 8.41° (d = 1.0510 nm, 110 crystal plane), 2θ = 13.80° (d = 0.6415 nm, 200 crystal plane), 2θ = 16.41° (d = 0.5400 nm, 130 crystal plane), and 2θ = 19.80° (d = 0.4819 nm, 400 crystal plane), respectively.

Figure 1

X-ray diffraction patterns of natural palygorskite (A) and zinc-bearing palygorskite (B). The raw palygorskite with the characteristic reflections appeared at 2θ = 8.41° (110, d = 1.0503 nm), 2θ = 13.72° (200, d = 0.6453 nm), 2θ = 16.37° (130, d = 0.5412 nm), and 2θ = 19.81° (400, d = 0.4482 nm), respectively. The heated palygorskite with the characteristic reflections appeared at 2θ = 8.47° (110, d = 1.0434 nm), 2θ = 13.71° (200, d = 0.6457 nm), 2θ = 16.42° (130, d = 0.5398 nm), and 2θ = 19.86° (400, d = 0.4470 nm), respectively. p = palygorskite, d = dolomite, q = quartz.

Table 1 shows the chemical composition of Pal and Zn-Pal. After being modified with ZnCl2, the content of Zn2+ ions of Zn-Pal increased, which is similar with the result by method of inductively coupled plasma mass spectrometry. It can be seen from Table 2 that the BET surface area of Pal is 164.29 m²/g, the cation exchange capacity of Pal is 28.01 mmol/100 g, the Zeta potential of Pal is −13.6 mV, and the BET surface area of Zn-Pal is 136.60 m²/g, the cation exchange capacity of Zn-Pal is 35.52 mmol/100 g, the Zeta potential of Zn-Pal is −15.5 mV.

Effect on gas production kinetics

Effect of Zn-Pal on GP at different times in vitro incubation is given in Table 4. While the other treatments became lower than that of the control staring at 3 h, the GP of the treatment I became higher at 9 h (p>0.05) and the gap tended to be stable with the extension of fermentation time, though no difference was shown between control and treatment groups. In addition, compared with treatment I, the GP of the treatment II, treatment III, and treatment IV became lower at 18, 24, 36, 48, 60, and 72 h (p<0.05) except the GP of the treatment IV has no significant difference at 60 and 72 h (p>0.05), meanwhile the GP of the treatment II has most significant difference at 24 and 36 h (p<0.01).

Table 4

Influence of zinc-bearing palygorskite on in vitro gas production

In vitro rumen fermentation parameters

Effects of Zn-Pal on pH, NH₃-N, MCP, and LPS profile values at different times of in vitro incubation are given in Table 5. Effects of Zn-Pal on VFAs profile value at different times of in vitro incubation are given in Table 6. Under this experiment, from 0 to 24 h, the pH was linearly decreased with the extension time of incubation and from 24 to 72 h, the pH was linearly increased with the extension time of incubation. The pH in the treatment IV became lower than in the control group at 6 h (p<0.05), while pH became higher at 24, 48, and 72 h (p<0.05, range 6 to 7), though no difference was shown between control and other treatment groups at 0 and 12 h (p>0.05).

Table 5

Influence of zinc-bearing palygorskite on rumen fermentation parameters

Table 6

Influence of zinc-bearing palygorskite on the production of VFA (mM/L)

The concentration of NH₃-N from 0 to 12 h was found no differences among the control and treatment groups (p>0.05). The concentration of NH₃-N in the treatment I, treatment II, and treatment III groups were higher than in the control group at 24 h (p<0.01), and the three treatment groups were lower than in the control group at 48 and 72 h (p<0.01), though no different significant was shown between control and other treatment groups at 24, 48, and 72 h (p>0.05).

The MCP synthesis in the treatment I was lower than control (p<0.05) and the MCP synthesis in the treatment III was higher than control (p<0.05), meanwhile, though no difference was shown between control and other treatments at 6 h. The MCP synthesis was significantly increased in the treatment I than that of control at 48 h (p<0.01), while other treatments also increased compared to the control at 12, 48, and 72 h, but there had no significant difference between them (p>0.05).

The concentration of LPS in the treatment I and treatment II were increased than control at 6 h (p<0.05). However, treatment III produced the lower concentration of LPS at 12 h compared to the control (p<0.05). The LPS concentration in treatment I was lower than control at 24, 48, and 72 h (p> 0.05), while other treatments was higher than control, although there had varying degrees of increase.

Acetate and total VFA in all treatments were higher than the control at all times, while there had significant difference at 24, 48, and 72 h (p<0.05). The amount of butyrate in treatment III were significantly lower than in the control at 6 h (p<0.05), while the level of propionate in all treatments were significantly higher than in the control at 24 h (p<0.05).

DISCUSSION

As shown in the XRD patterns (Figure 1), there is no obvious difference among the scattering peaks from the two samples, and only the intensity of reflections at 1.05, 0.54, and 0.45 nm weaken slightly, because of the removal of partial zeolite water from the tunnel of palygorskite during thermal treatment process [17], indicating that zinc-bearing can keep the basic crystal structure of palygorskite. Moreover, there is no new crystal phase generates during modification process, which reveals that Zn²⁺ ions interact with palygorskite by an ion-exchange process. The change of BET surface area and cation exchange capacity is due to the process of zinc-bearing. The change of zeta potential is due to the dissociation and dispersion of palygorskite crystal beam and the exchange of sodium ions with metal ions on the surface of palygorskite.

In current study, the Zeta potentials of Pal and Zn-Pal samples are all negative and became more negative after Zn-bearing. The increase of negative charges is favorable to enhance the affinity of palygorskite with cationic matters, e.g., cationic dyes, and then improve the adsorption for them. Marchuk et al [18] have proved that palygorskite particle could be considered as an anion with large size and high charge density, which attracts the ions of opposite sign and repels the ions of the same sign of the particle). Hamieh et al [19] have proved that the negatively charged rod-crystals were surrounded by opposite ions and the surface potential of particle decreased, when palygorskite was dispersed in various solutions containing inorganic ions. The thickness of the diffuse layer might reduce due to increase in the concentration of electrolyte, while at the same ion valency [20]. Therefore, the difference in the physico-chemical property and the amount of Zn²⁺ of Zn-Pal might indicate different effects in rumen fermentation.

The GP is a comprehensive indicator for reflecting the degree of ruminal fermentation. GP has been proven to be positively related to the activity of ruminal bacteria [21]. Meanwhile, higher microbial activity and GP are often accompanied by a stronger fermentation level of fodder. As the fermentation time goes on, the GP in the treatment groups was increased first and then decreased, possibly because the nutrients in the substrate were beneficial to the growth of bacteria, the number of fungi gradually decreased until disappeared, resulting in an increase in GP; fermentation substrates are limited, limiting the number and activity of bacteria and thus resulting in reduced GP. In current study, the GP of the treatment I became higher starting at 9 h. The result indicated that a low dose of Zn-Pal increased the GP in the rumen, which is beneficial for the health of the ruminant. A high level of Zn-Pal has no significant effect on GP. The main reason might be that Zeta potential of Zn-Pal becomes more negative, which promotes the adsorption of Zn-Pal.

pH is an important parameter that keeps the balance of rumen microbes and reflects the extent and pattern of diet fermentation. Normal ruminal pH values range from 6 to 7. If the value is too low or too high, is not conducive to the growth of rumen microorganisms, which greatly affect the physiological function of animals. In general, rumen pH decreased after feeding, and then gradually increased, ruminal pH fluctuated and changes, pH fluctuations in the curve reflects the concentration of organic acids and produce saliva changes. In current study, the pH in the treatment groups became higher than in the control group at 24, 48, and 72 h. Meanwhile, all values were in the normal range. This result indicated that adding Zn-Pal was beneficial to dairy cows by increasing the ruminal pH. This finding is consistent with the result of Ehrlich et al [22], who reported that adding 4% sodium bentonite or 2% zeolite could also increase pH and improve the ruminal health of cows. In addition, the ion-exchange property of the clay could alter the pH and the ionic composition (including trace elements) of the gastrointestinal fluids, resulting in enhanced enzymatic activity, and this is beneficial for ruminal microbial fermentation [23]. Then, the Zn-Pal increased the pH in the rumen, which is beneficial for the health of the ruminant.

Ammonia concentration in the rumen is a balance between degradation of feed protein and uptake of ammonia for synthesis of microbial protein. In the rumen microflora, about 80% of the bacteria treat ammonia nitrogen as a direct nitrogen source. In this study, adding Zn-Pal could promote the release of NH₃-N and the synthesis of MCP. Kennedy [7] have reported that adding the content of Zn in diet can reduce the concentration of NH₃-N, promote cell protein synthesis. In addition, Kardaya [24] have suggested that nanoporous structure of zeolite could cause the release of ammonia and maintain the stability of ammonia concentrations because of their sustained release and cation-exchange capacity. In the present study, Zn-Pal has more cation-exchange capacity than palygorskite. This finding is consistent with the result of Zeng et al [25], who reported that adding 3% palygorskite or heated palygorskite in vitro was beneficial for nitrogen use and MCP synthesis. It has also proved that milk protein yield increased with 10 kg/t of supplemental dietary palygorskite in diets [26]. Therefore, adding Zn-Pal was beneficial for nitrogen use and MCP synthesis, and the Zn-Pal showed better stability than the palygorskite. In addition, Zn-Pal is rich in Zn²⁺, Al³⁺, and Mg²⁺ and has a strong cation-exchange capacity, which might affect the corresponding ion concentrations in rumen. It has also been proven that supplemental 23 g/kg of zeolite in the cow diet can improve ruminal Al³⁺ concentrations [27].

The VFAs are the products of microbial fermentation of carbohydrates in the rumen and represent the main supply of metabolizable energy for ruminants [28]. In this study, acetate and total VFA were increased by supplementing Zn-Pal. Palygorskite has similarity structure and biological characteristics with natural silicate, as do minerals such as bentonite, zeolite and montmorillonite. Salem et al [29] reported the addition of 12 g/d of bentonite to the sheep diet resulted in an increase of total VFA. Zeng et al [25] showed palygorskite and heated palygorskite supplementation increased VFA concentrations in the rumen. All of these results indicate that silicate could improve rumen fermentation and VFA formation. In the present study, the Zeta potential of Zn-Pal becomes more negative, which promotes the adsorption of palygorskite. Therefore, Zn-Pal has a higher adsorption capacity than palygorskite, which could provide a stable internal environment in which more beneficial bacteria exist, improving carbohydrate decomposition and increasing VFAs [30].

The LSP is the product of the cell wall of Gram-negative bacteria, which are the predominant bacterial group in the rumen. Plaizier et al [31] has revealed that a decline in ruminal pH causes the death and cell lysis of gram-negative bacteria, resulting in an increase in the free ruminal LPS concentration. In addition, the increased in the free ruminal LPS concentration may also be caused by the rapid growth of bacteria. In current study, compared with control, the LPS concentration in treatment I rised first and then lower with time, meanwhile, the LPS concentration in other treatment groups become lower at 12 and 24 h. Zinc is the body of the necessary trace elements, but also has a certain antibacterial propertie [32]. The release of Zn²⁺ from the surface or the pores of the earth is negatively charged with a negatively charged microbial cell membrane that destroys the activity of the cell synthase and interferes with the DNA synthesis, resulting in the loss of the microorganism and the ability to divide and proliferate [33] Abend et al [34] have proved that montmorillonite has a unique charge characteristic, which has a lasting effect. Researcher has found that adding 0.2% montmorillonite to the diet can reduce the LPS concentration in digestive segments of chyme, except for cecum [35].

CONCLUSION

In conclusion, the zinc-bearing treatment process not merely maintained the crystal structure of palygorskite, but also increased the cation exchange and the content of zinc ion. Addition of Zn-Pal can improve rumen fermentation, promote VFA formation, MCP synthetic, and LPS adsorb by promoting the release of Zn, especially when adding 0.2% Zn-Pal.

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