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Article

Effects of Supplemental Benzoic Acid, Bromelain, Adipic Acid, and Humic Substances on Nitrogen Utilization, Urine pH, Slurry pH, and Manure Odorous Compounds in Pigs

1
Department of Animal Science, Konkuk University, Seoul 05029, Republic of Korea
2
Animal Environmental Division, National Institute of Animal Science, Wanju 55365, Republic of Korea
*
Author to whom correspondence should be addressed.
Animals 2024, 14(1), 82; https://doi.org/10.3390/ani14010082
Submission received: 3 December 2023 / Revised: 20 December 2023 / Accepted: 22 December 2023 / Published: 25 December 2023
(This article belongs to the Section Animal Nutrition)

Abstract

:

Simple Summary

Ammonia gases are produced from urea in the urine and slurry due to the action of urease. Odorous compounds are produced by microbial fermentation that utilizes an undigested nutrient in pig slurry. Various additives have been researched to mitigate ammonia emissions or odorous compound production. These studies involve inducing acidic conditions in urine or slurry, enhancing nitrogen utilization, inhibiting urease, or absorbing odorous compounds in pig slurry. However, information about the comparison of these additives is lacking. In this study, we evaluate and compare the effects of each additive on nitrogen utilization, urinary pH, slurry pH, and odorous compound concentrations. The five experimental diets were (1) a control diet, (2) the control diet with 1% benzoic acid, (3) the control diet with 1% adipic acid, (4) the control diet with 1% bromelain, and (5) the control diet with 1% humic substances. Fecal dry matter and nitrogen output were greatest in pigs fed the humic substances diet. Daily retained nitrogen and the nitrogen retention rate tended to be lowest in pigs fed an adipic acid diet. Urinary pH was lowest in pigs fed the adipic acid diet. In addition, slurry pH did not affect odorous compound concentrations, and some odorous compounds tended to be lowest in pigs fed the humic substances diet.

Abstract

The objective was to evaluate the effects of benzoic acid, bromelain, adipic acid, and humic substance supplementation on nitrogen balance, urinary pH, slurry pH, and manure odorous compounds in pigs. Fifteen castrated male pigs with an initial body weight of 37.9 kg (standard deviation = 4.1) were individually housed in metabolism crates. The animals were allocated to a triplicated 5 × 2 incomplete Latin square design with 15 animals, 5 experimental diets, and 2 periods. The basal diet mainly consisted of corn, soybean meal, and rapeseed meal. Four experimental diets were prepared by supplementing each additive at a concentration of 10 g/kg at the expense of corn starch to the basal diet. Each period consisted of a 4-day adaptation period, a 24 h collection period for slurry sampling, and a 4-day collection period for feces and urine. The feces and urine collected for 24 h on day 5 were mixed at a ratio of fecal weight and urine weight to obtain slurry samples. The apparent total tract digestibility N in pigs fed the humic substance diet was the least (p < 0.05) compared to the other groups. The daily retained N and N retention as % ingested tended (p < 0.10) to be the lowest in the adipic acid group among the treatments. The urinary pH in pigs fed the adipic acid diet was less (p < 0.05) than that in other groups except the benzoic acid group. The slurry pH tended to differ among the treatment groups (p = 0.074) with the lowest value in the pigs fed the adipic acid diet. The concentrations of indole in slurry (p = 0.084) and isovalerate in feces (p = 0.062) tended to differ among the groups with the lowest values in the pigs fed the humic substance diet. In conclusion, adipic acid supplementation in pig diets can decrease urinary pH and slurry pH. Although benzoic acid and adipic acid have limited effects in reducing odorous compounds, humic substances have the potential to reduce some odorous compounds.

1. Introduction

In the swine industry, the release of ammonia gases and offensive odorous compounds, including volatile fatty acids (VFA) and volatile organic compounds, has been noticed due to environmental issues. Ammonia gases are produced in pig slurry due to the hydrolysis of urea by the action of urease [1]. The emission of ammonia gases results in the formation of fine particulates and the eutrophication of ecosystems [2]. The odorous compounds are generated by the microbial fermentation of undigested nutrients in the slurry [3], and these compounds are potential challenges to public health [4]. Therefore, efforts to reduce odorous compounds emitted from pig slurry are important to ensure sustainable livestock farming. Thus, research on effective strategies for reducing ammonia and odorous compounds has been conducted [5,6,7]. Supplemental organic acids such as benzoic acid (BA), an aromatic carboxylic acid, and adipic acid, a dicarboxylic acid with a six-carbon chain, in swine diets have been reported to be excreted through urine and, consequently, lower the pH of urine to prevent the degradation of urea to ammonia [8,9,10]. In addition, BA has been reported to decrease nitrogen (N) excretion by improving N utilization [11,12]. Supplemental protease is also considered one of the methods to reduce fecal N excretion from pigs by improving protein digestion and absorption [13]. Bromelain is a proteolytic enzyme extracted from pineapple. Humic substances (HS) consisted of humic acid, fulvic acid, and inorganic compounds derived from soil have also been suggested to reduce the ammonia emission from pig manure by inhibiting urease activity [14] and to reduce the odorous compounds in pig manure [15].
Although BA, adipic acid, bromelain, and HS may reduce odorous compounds and ammonia from the slurry in a pig house, the effects of these additives have not been compared. Therefore, the objective of this study was to determine the effects of supplemental BA, adipic acid, bromelain, and HS to diets on the N balance, urinary pH, slurry pH, and odorous compound concentrations in pig manure.

2. Materials and Methods

All protocols for the animal experiment were reviewed and approved by the Institutional Animal Care and Use Committee of Konkuk University (Seoul, Republic of Korea, KU23055).

2.1. Animals, Experimental Design, and Diets

Fifteen castrated male pigs (Landrace × Yorkshire) with an initial mean body weight of 37.9 kg (standard deviation = 4.1) were allotted to a triplicated 5 × 2 incomplete Latin square design with 15 animals, 5 experimental diets, and 2 periods to obtain 6 observations per treatment. A spreadsheet-based program was used to minimize potential carryover effects [16]. Pigs were individually housed in metabolism crates equipped with a feeder and a nipple drinker. The five dietary treatments were (1) a control diet, (2) the control diet + 1% BA, (3) the control diet + 1% adipic acid, (4) the control diet + 1% bromelain, and (5) the control diet + 1% HS (Table 1). All experimental diets were formulated based on corn, soybean meal, and rapeseed meal. The experimental diets were formulated to meet or exceed the nutrient requirement estimates suggested by the NRC [17]. Each additive was supplemented to the control diet at the expense of corn starch.

2.2. Feeding and Sample Collection

Using the body weight of each pig and the metabolizable energy concentrations of the experimental diets, daily feed allotments were calculated at the beginning of each experimental period as 3 times the maintenance energy requirement (i.e., 197 kcal of metabolizable energy per kg of body weight0.60) [18]. The amount of feed allotment was divided into 2 equal quantities and provided to pigs at 0800 and 1700 h. Water was freely available at all times.
The experimental period consisted of a 4-day adaptation period, a 24 h collection period for slurry sampling, and a 4-day collection period for fecal and urine collection [19]. The feces and urine collected for 24 h on day 5 were mixed at a ratio of fecal weight and urine weight to obtain slurry samples. On days 6 and 10, chromic oxide was added as a marker at 0.5% to the morning meals. The marker-to-marker procedure was employed for the total collection of feces [19]. The fecal collection started when the green color of chromium began to appear in the feces and ended when the green color appeared again. Urine collection was initiated at 1000 h on day 6 and terminated at 1000 h on day 10. Urine was weighted and collected twice daily at 1000 h and 1900 h. The urinary and slurry pH were measured using a pH meter (PM-2, CAS Inc., Yangju, Gyung-gi, Republic of Korea) immediately after weighing urine. All feces and urine samples were stored at −20 °C immediately after collection.

2.3. Volatile Fatty Acid Analyses

For the VFA analysis, 1 mL of a 25% meta-phosphoric acid solution (Sigma-Aldrich, St. Louis, MO, USA) was added to each of 5 g of feces and 5 mL of slurry in a 15 mL plastic tube, and 0.05 mL of a saturated mercury (II) chloride solution (Sigma-Aldrich, St. Louis, MO, USA) was also added to the plastic tube. Then, the solution was centrifuged at 3134× g for 20 min at 20 °C, and then 1 mL of supernatant was collected. The supernatant was also centrifuged for 10 min at 13,800× g and filtered through a 0.2-μm Whatman filter (Whatman, Uppsala, Sweden). The filtrates were transferred to 2 mL gas chromatography vials (Agilent, Santa Clara, CA, USA). The concentration of VFA was determined using a gas chromatograph (6890N, Agilent, Santa Clara, CA, USA) that was equipped with an HP-INNOWax column (30 m × 0.25 mm × 0.25 μm; Agilent, Santa Clara, CA, USA) and a flame ionization detector. A sample of 0.2 μL was injected at a 10-to-1 split ratio. The gas chromatography oven was initially set at 80 °C for 2 min and increased to 120 °C at a rate of 20 °C per min. The oven temperature was then increased to 205 °C at 10 °C per min, and finally held at 205 °C for 2 min. The injection and detection ports of gas chromatography were maintained at 250 °C.

2.4. Phenol and Indole Analyses

After centrifuging the fecal and slurry samples at 3134× g for 20 min at 20 °C, 4 mL of supernatant was collected. The supernatant was placed in a 20-mL glass vial, and then 4 mL of chloroform (Merck, Darmstadt, Germany) and 60 μL of 4 M sodium hydroxide solution (Sigma-Aldrich, St. Louis, MO, USA) were also added to the glass vial and mixed with supernatant. The mixture in the glass vial was centrifuged at 3134× g for 20 min at 20 °C, and the chloroform layer was collected and placed into a 2.0-mL gas chromatography vial (Agilent, Santa Clara, CA, USA). Phenols and indoles in the chloroform layer were determined using a gas chromatograph (6890N, Agilent, Santa Clara, CA, USA) that was equipped with a DB-1 column (30 m × 0.25 mm × 0.25 μm, Agilent, Santa Clara, CA, USA) and a flame ionization detector. A sample of 2.0 μL was injected at a 5-to-1 split ratio. The gas chromatography oven was initially set at 40 °C for 5 min, increased to 230 °C at a rate of 10 °C per min, and finally held at 230 °C for 2 min. The injection and detection ports of gas chromatography were maintained at 250 °C.

2.5. Chemical Analyses

The fecal samples were dried in a forced-air drying oven at 55 °C until constant weight was achieved and ground before analysis. Samples of ingredients, diets, and feces were analyzed for dry matter (DM; [20]) and ash (method 942.05) according to the AOAC [21]. Samples of ingredients, diets, feces, and urine were analyzed for crude protein (method 990.03). Gross energy in the diet samples was determined using bomb calorimetry (Parr 6200, Parr Instruments Co., Moline, IL, USA). Amylase-treated neutral detergent fiber (method 2002.04) and acid detergent fiber (method 973.18) in the diets were analyzed according to the AOAC [21].

2.6. Calculations

The apparent total tract digestibility (ATTD) of DM and N was calculated using the following equations:
ATTD of DM (%) = [(DMintake − DMfeces) ÷ DMintake] × 100
ATTD of N (%) = [(Nintake − Nfeces) ÷ Nintake] × 100
where DMintake and DMfeces represent the amount of DM intake (g/d) and fecal DM output (g/d), respectively, and Nintake and Nfeces represent the amount of N intake (g/d) and fecal N output (g/d), respectively. The balance of N in pigs fed experimental diets was calculated using the following equations:
N retention rate as % of ingested (%) = 100 × (Nintake − Nfeces − Nurine) ÷ Nintake
N retention rate as % of digested (%) = 100 × (Nintake − Nfeces − Nurine) ÷ (Nintake − Nfeces)
where Nintake, Nfeces, and Nurine represent the amount of N intake (g/d), fecal N output (g/d), and urinary N output (g/d), respectively.

2.7. Statistical Analyses

Experimental data were statistically analyzed using the MIXED procedures of SAS (SAS Inst. Inc., Cary, NC, USA). The statistical model included the experimental diet as the fixed variable and replication and period within replication as the random variables. Least-square means were calculated, and the means were separated using the PDIFF option. An individual pig was the experimental unit, and statistical significance and tendency were declared at p < 0.05 and 0.05 ≤ p < 0.10, respectively.

3. Results

All the pigs were in good health throughout the experiment and readily consumed their daily feed allowance. The ATTD of DM and N in pigs fed the HS diet was less (p < 0.05) than those fed the control diet (Table 2). The daily retained N and N retention as % ingested tended (p < 0.10) to be the greatest in the BA group and the lowest in the adipic acid group among the treatments.
The urinary pH in pigs fed the adipic acid diet was less (p < 0.05) than the control, the bromelain group, and the HS group but did not differ from the BA diet (Table 3). The slurry pH in pigs fed the adipic acid diet tended to be the lowest (p = 0.074) among experimental diets.
The VFA concentrations in feces and slurry were not different among pigs fed the experimental diets (Table 4). However, the isovalerate concentrations in feces (p = 0.062) and the indole in slurry tended to be the lowest (p = 0.084) in pigs fed the HS diet among experimental diets.

4. Discussion

Benzoic acid is one of the organic acids that have been reported to improve the environment of the gastrointestinal tract and growth performance [22,23]. Patráš et al. [24] reported a tendency for N retention to improve due to 1% dietary BA inclusion. Murphy et al. [25] also reported a linear increase in N retention in response to feeding BA at 0, 1%, 2%, and 3% to pigs. The supplementation of organic acids has been suggested to improve N utilization by lowering the pH in the stomach [26,27]. Pepsin is activated at an acidic condition, and thus, supplemental acids can improve N digestibility by lowering gastric pH, which likely affects N metabolism in pigs [28]. In this study, however, supplemental BA did not affect N balance, which is inconsistent with the previous studies. The reason for the inconsistency among the studies remains unclear, but the different ingredient compositions in diets potentially resulted in varying acid-binding capacities of diets in the stomach [29]. Patráš et al. [24] used 43 to 57% corn, 30% wheat, and 8 to 22% soybean meal as the main ingredients and Murphy et al. [25] used 35 to 38% wheat, 25% barley, 17% soybean meal, and 15% corn, whereas the diets in the present experiment were based on 68% corn, 17% soybean meal, and 10% rapeseed meal. Corn has been suggested to have a greater acid-binding capacity compared with wheat [29], which may have resulted in the lack of effects of BA on N balance in the present work. Furthermore, this suggestion is supported by Bühler et al. [30] who reported that dietary BA did not have an effect on the N balance in pigs fed a diet containing 20% barley, which has a greater acid-binding capacity compared with corn or wheat. Additionally, variations in experimental conditions can also potentially affect the effects of supplemental BA in pigs.
The decreases in daily retained N and the N retention rate of the adipic acid group in the present study may be explained by the toxic properties of adipic acid [31]. Administering adipic acid to rats induced an increased lavage protein in their bodies [31], which suggests that adipic acid in animal bodies may act as a toxic material. Adverse effects of supplemental adipic acid on the growth performance of pigs [28] and lysine utilization in pigs [32] have also been reported. Dietary adipic acid appears to decrease N utilization in pigs due to additional protein synthesis for eliminating adipic acid toxicity.
Bromelain is a protease that breaks down polypeptide compounds. Bromelain has been reported to improve N digestibility, and consequently, reduce fecal N excretion and noxious gas emission in nursery pigs [33,34]. In the present work, however, supplemental bromelain did not improve N digestibility in growing pigs, which is likely due to the different growth stages of pigs. Mc Alpine et al. [35] also failed to find the effects of supplemental protease on N digestibility in finishing pigs. It appears that a sufficient quantity of protease is secreted for the digestion of dietary protein in growing and finishing pigs but not in nursery pigs based on the greater protein digestibility in older pigs compared with nursery pigs [36,37]. Therefore, the lack of positive effects of bromelain on N digestibility in the present work is reasonable. In addition, Nguyen et al. [34] also reported that supplemental bromelain or other protease showed positive effects on N digestibility of nursery pigs but not in growing and finishing pigs.
Humic substances consist of humic acids, fulvic acids, and several inorganic substances derived from the soil or sediment. Humic substances themselves contain significant amounts of N, which is not easily degraded [38]. This may partially explain the low N digestibility in the HS group in the present study. Additionally, HS can bind various materials such as minerals and amino acids in diets [39,40], resulting in the inhibition of enzymatic digestion or microbial action against these nutrients. In agreement with the present results, Písaříková et al. [40] noted a 6% reduction in N digestibility via the supplementation of 3% sodium humate in pigs.
Most previous studies reported a reduction in urinary pH by supplemental BA [24,25,30,41,42]. Supplemental BA in pig diets is known to decrease urinary pH as BA is converted into hippuric acid in the liver and excreted in the urine [43]. However, the effect of supplemental BA on urinary pH was not significant in the present work. The inconsistency between this study and the literature may be partially attributed to the different methods used for urine collection. The urine samples were collected directly from the bladder after euthanizing pigs [41,44] or through an equipped catheter [24,45] in previous studies. In the present work, in contrast, urine was collected in containers, and time-based sampling was conducted 2 times per day during collection periods, allowing for more exposure of urine stored in containers to external factors such as air and microbial action [30]. Additionally, water intake may also have contributed to the hippuric acid concentration and pH of urine. Indeed, a positive correlation between the weight of urine and urinary pH was observed in pigs fed the BA diet in the present work (r = 0.39 and p = 0.002). Further research is warranted to investigate the interaction between water intake and urinary pH.
Adipic acid is a type of dicarboxylic acid consisted of six carbon atoms derived from longer-chained dicarboxylic acids after beta-oxidation reactions [46]. Adipic acid ingested by pigs is excreted per se or after degradation into shorter dicarboxylic acids through the urine [46], resulting in decreased urinary pH and slurry pH [47]. In agreement, the urinary pH and slurry pH were reduced by supplemental adipic acid in the present study.
Odorous compounds in pig manure are generally produced by microbiota that decompose manure [48]. As microbial genera in manure thrive under an environment of optimum pH, modifying manure pH can weaken microbial action and decrease odorous compound production. Jensen et al. [49] observed decreases in indole and skatole production when modifying the pH of pig slurry below 5 or above 8 by deactivating microbes. Zhu and Jacobson [48] also suggested that the optimal pH for microbial growth ranges from 5.0 to 8.5. The slurry pH in all treatment groups in the present study was within the range that provides the optimal environment for microbiota, supporting the lack of difference in odorous compound concentrations among treatment groups, except indole in the HS group.
The observation of no decrease in odorous compound concentrations in feces by supplemental bromelain is most likely due to the lack of changes in N digestibility. Most odorous compounds are produced from undigested amino acids or N compounds [6,50,51].
The tendency for the reduction in isovalerate in feces and indole in slurry from pigs fed the HS diet remains unclear because other odorous compounds were not affected by supplementing HS. In a previous study, however, Propionibacterium genera were reported to utilize humic acid as a terminal electron acceptor in the bacterial culture medium [52]. Benz et al. [53] also observed that Propionibacterium freudenreichii degraded propionate to acetate by using humic acid as a terminal electron acceptor. Therefore, the presence of HS might have encouraged Propionibacterium to further degrade isovalerate to produce lower-molecule compounds, resulting in the decreased isovalerate concentration in the present study. The role of HS might also partially explain the decrease in the indole concentration of slurry because indole can be degraded by anaerobic microbial fermentation [54]. Further research is warranted to investigate the mechanisms of HS during anaerobic microbial fermentation against odorous compounds.

5. Conclusions

The effects of supplemental additives on nitrogen utilization, urinary pH, slurry pH, and odorous compounds varied. Supplementing benzoic acid at 1% did not decrease urinary pH and slurry pH, whereas adipic acid at 1% lowered urinary pH in growing pigs. Supplementing humic substances at 1% negatively affected the nutrient digestibility but tended to decrease some odorous compound concentrations in feces and slurry. Overall, supplemental adipic acid was beneficial for lowering urinary pH and humic substances were effective in reducing odorous compounds in pig manure.

Author Contributions

Conceptualization, S.S. and B.G.K.; formal analysis, S.B.Y. and S.S.; investigation, S.B.Y.; visualization, S.B.Y.; validation, B.G.K. and Y.S.S.; writing—original draft preparation, S.B.Y.; writing—review and editing, B.G.K. and Y.S.S.; supervision, B.G.K. All authors have read and agreed to the published version of the manuscript.

Funding

This work was carried out with the support of “Cooperative Research Program for Agriculture Science & Technology Development (Project No. PJ017087)” Rural Development Administration, Republic of Korea.

Institutional Review Board Statement

All protocols for the animal experiment were reviewed and approved by the Institutional Animal Care and Use Committee of Konkuk University (Seoul, Republic of Korea, KU23055).

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in the current work are available.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Tabase, R.K.; Naess, G.; Larring, Y. Ammonia and methane emissions from small herd cattle buildings in a cold climate. Sci. Total Environ. 2023, 903, 166046. [Google Scholar] [CrossRef] [PubMed]
  2. Krupa, S.V. Effects of atmospheric ammonia (NH3) on terrestrial vegetation: A review. Environ. Pollut. 2003, 124, 179–221. [Google Scholar] [CrossRef] [PubMed]
  3. Hwang, O.H.; Cho, S.B.; Han, D.W.; Lee, S.R.; Kwag, J.H.; Park, S.K. Effect of storage period on the changes of odorous compound concentrations and bacterial ecology for identifying the cause of odor production from pig slurry. PLoS ONE 2016, 11, e0162714. [Google Scholar] [CrossRef] [PubMed]
  4. Cole, D.; Todd, L.; Wing, S. Concentrated swine feeding operations and public health: A review of occupational and community health effects. Environ. Health Perspect. 2000, 108, 685–699. [Google Scholar] [CrossRef] [PubMed]
  5. Philippe, F.X.; Cabaraux, J.F.; Nicks, B. Ammonia emissions from pig houses: Influencing factors and mitigation techniques. Agric. Ecosyst. Environ. 2011, 141, 245–260. [Google Scholar] [CrossRef]
  6. Sutton, A.L.; Kephart, K.B.; Verstegen, M.W.A.; Canh, T.T.; Hobbs, P.J. Potential for reduction of odorous compounds in swine manure through diet modification. J. Anim. Sci. 1999, 77, 430–439. [Google Scholar] [CrossRef]
  7. Kim, J.H.; Ko, G.P.; Son, K.H.; Ku, B.H.; Bang, M.A.; Kang, M.J.; Park, H.Y. Arazyme in combination with dietary carbohydrolases influences odor emission and gut microbiome in growing-finishing pigs. Sci. Total Environ. 2022, 848, 157735. [Google Scholar] [CrossRef]
  8. Melse, R.W. Air Treatment Techniques for Abatement of Emissions from Intensive Livestock Production; Wageningen University and Research: Wageningen, The Netherlands, 2009. [Google Scholar]
  9. Kim, J.; Hong, B.; Lee, M.J.; Kim, B.G. Demonstration of constant nitrogen and energy amounts in pig urine under acidic conditions at room temperature and determination of the minimum amount of hydrochloric acid required for nitrogen preservation in pig urine. Anim. Biosci. 2023, 36, 492–497. [Google Scholar] [CrossRef]
  10. Liu, J.; Li, X.; Xu, Y.; Wu, Y.; Wang, R.; Zhang, X.; Hou, Y.; Qu, H.; Wang, L.; He, M.; et al. Highly efficient reduction of ammonia emissions from livestock waste by the synergy of novel manure acidification and inhibition of ureolytic bacteria. Environ. Int. 2023, 172, 107768. [Google Scholar] [CrossRef]
  11. Partanen, K.H.; Mroz, Z. Organic acids for performance enhancement in pig diets. Nutr. Res. Rev. 1999, 12, 117–145. [Google Scholar] [CrossRef]
  12. Gräber, T.; Kluge, H.; Hirche, F.; Brož, J.; Stangl, G.I. Effects of dietary benzoic acid and sodium-benzoate on performance, nitrogen and mineral balance and hippuric acid excretion of piglets. Arch. Anim. Nutr. 2012, 66, 227–236. [Google Scholar] [CrossRef] [PubMed]
  13. Kim, Y.J.; Kim, T.H.; Song, M.H.; An, J.S.; Yun, W.; Lee, J.H.; Oh, H.J.; Lee, J.S.; Kim, G.M.; Kim, H.B.; et al. Effects of different levels of crude protein and protease on nitrogen utilization, nutrient digestibility, and growth performance in growing pigs. J. Anim. Sci. Technol. 2020, 62, 659–667. [Google Scholar] [CrossRef] [PubMed]
  14. Ji, F.; McGlone, J.J.; Kim, S.W. Effects of dietary humic substances on pig growth performance, carcass characteristics, and ammonia emission. J. Anim. Sci. 2006, 84, 2482–2490. [Google Scholar] [CrossRef] [PubMed]
  15. Loyola Andrade, N.A. Effects of Humic Acids Supplementation on Pig Growth Performance, Nitrogen Digestibility, Odor and Ammonia Emission. Bachelor’s Thesis, Universidad San Francisco de Quito, Colegio de Ciencias de la Salud, Quito, Ecuador, 2019. [Google Scholar]
  16. Kim, B.G.; Stein, H.H. A spreadsheet program for making a balanced Latin square design. Rev. Colomb. Cienc. Pec. 2009, 22, 591–596. [Google Scholar]
  17. NRC. Nutrient Requirements of Swine, 11th ed.; National Academies Press: Washington, DC, USA, 2012. [Google Scholar]
  18. Lee, S.A.; Kong, C.; Adeola, O.; Kim, B.G. Different coefficients and exponents for metabolic body weight in a model to estimate individual feed intake for growing-finishing pigs. Asian-Australas. J. Anim. Sci. 2016, 29, 1756–1760. [Google Scholar] [CrossRef] [PubMed]
  19. Choi, H.; Kim, B.G. A low-fiber diet requires a longer adaptation period before collecting feces of pigs compared with a high-fiber diet in digestibility experiments using the inert marker method. Anim. Feed Sci. Technol. 2019, 256, 114254. [Google Scholar] [CrossRef]
  20. Ahn, J.Y.; Kil, D.Y.; Kong, C.; Kim, B.G. Comparison of oven-drying methods for determination of moisture content in feed ingredients. Asian-Australas. J. Anim. Sci. 2014, 27, 1615–1622. [Google Scholar] [CrossRef]
  21. AOAC. Official Methods of Analysis, 21st ed.; Association of Official Analytical Chemists International: Gaithersburg, MD, USA, 2019. [Google Scholar]
  22. Warner, A.J.; DeRouchey, J.M.; Tokach, M.D.; Woodworth, J.C.; Goodband, R.D.; Gebhardt, J.T. Effect of added calcium carbonate without and with benzoic acid on weanling pig growth performance, fecal dry matter, and blood Ca and P concentrations. Transl. Anim. Sci. 2023, 7, txad055. [Google Scholar] [CrossRef]
  23. Goh, T.W.; Hong, J.; You, D.H.; Han, Y.G.; Nam, S.O.; Kim, Y.Y. Effects of medium chain triglycerides with organic acids on growth performance, fecal score, blood profiles, intestinal morphology, and nutrient digestibility in weaning pigs. Anim. Biosci. 2022, 35, 916–926. [Google Scholar] [CrossRef]
  24. Patráš, P.; Nitrayová, S.; BreSteNSký, M.; Heger, J. The effects of benzoic acid and protein level on urine ph and ammonia emission of pigs. Slovak J. Anim. Sci. 2014, 47, 100–104. [Google Scholar]
  25. Murphy, D.P.; O’Doherty, J.V.; Boland, T.M.; O’Shea, C.J.; Callan, J.J.; Pierce, K.M.; Lynch, M.B. The effect of benzoic acid concentration on nitrogen metabolism, manure ammonia and odour emissions in finishing pigs. Anim. Feed Sci. Technol. 2011, 163, 194–199. [Google Scholar] [CrossRef]
  26. Zhong, Y.; Zuo, B.; Li, J.Z.; Zhai, Y.; Mudarra, R. Effects of paraformic acid supplementation, as an antibiotic replacement, on growth performance, intestinal morphology and gut microbiota of nursery pigs. J. Anim. Sci. Technol. 2023. [Google Scholar] [CrossRef]
  27. Suiryanrayna, M.V.; Ramana, J.V. A review of the effects of dietary organic acids fed to swine. J. Anim. Sci. Biotechnol. 2015, 6, 45. [Google Scholar] [CrossRef] [PubMed]
  28. Roth, F.X.; Kirchgessner, M. Organic acids as feed additives for young pigs: Nutritional and gastrointestinal effects. J. Anim. Feed Sci. 1998, 7, 25–33. [Google Scholar] [CrossRef]
  29. Lawlor, P.G.; Lynch, P.B.; Caffrey, P.J.; O’Reilly, J.J.; O’Connell, M.K. Measurements of the acid-binding capacity of ingredients used in pig diets. Ir. Vet. J. 2005, 58, 447–452. [Google Scholar] [CrossRef]
  30. Bühler, K.; Wenk, C.; Broz, J.; Gebert, S. Influence of benzoic acid and dietary protein level on performance, nitrogen metabolism and urinary pH in growing-finishing pigs. Arch. Anim. Nutr. 2006, 60, 382–389. [Google Scholar] [CrossRef]
  31. Kennedy, G.L., Jr. Toxicity of adipic acid. Drug Chem. Toxicol. 2002, 25, 191–202. [Google Scholar] [CrossRef]
  32. van Kempen, T.A.; van Heugten, E.; Trottier, N.L. Adipic acid increases plasma lysine but does not improve the efficiency of lysine utilization in swine. J. Anim. Sci. 2001, 79, 2406–2411. [Google Scholar] [CrossRef]
  33. Hossain, M.M.; Lee, S.I.; Kim, I.H. Effects of bromelain supplementation on growth performance, nutrient digestibility, blood profiles, faecal microbial shedding, faecal score and faecal noxious gas emission in weanling pigs. Vet. Med. 2015, 60, 544–552. [Google Scholar] [CrossRef]
  34. Nguyen, D.H.; Lee, S.I.; Cheong, J.Y.; Kim, I.H. Influence of low-protein diets and protease and bromelain supplementation on growth performance, nutrient digestibility, blood urine nitrogen, creatinine, and faecal noxious gas in growing-finishing pigs. Can. J. Anim. Sci. 2018, 98, 488–497. [Google Scholar] [CrossRef]
  35. Mc Alpine, P.O.; O’Shea, C.J.; Varley, P.F.; O’Doherty, J.V. The effect of protease and xylanase enzymes on growth performance and nutrient digestibility in finisher pigs. J. Anim. Sci. 2012, 90 (Suppl. S4), 375–377. [Google Scholar] [CrossRef] [PubMed]
  36. Mavromichalis, I.; Hancock, J.D.; Senne, B.W.; Gugle, T.L.; Kennedy, G.A.; Hines, R.H.; Wyatt, C.L. Enzyme supplementation and particle size of wheat in diets for nursery and finishing pigs. J. Anim. Sci. 2000, 78, 3086–3095. [Google Scholar] [CrossRef] [PubMed]
  37. Urbaityte, R.; Mosenthin, R.; Eklund, M.; Piepho, H.P.; Sauer, N.; Rademacher, M. Standardised ileal crude protein and amino acid digestibilities in protein supplements for piglets. Arch. Anim. Nutr. 2009, 63, 356–378. [Google Scholar] [CrossRef]
  38. Stevenson, F.J. Humus Chemistry: Genesis, Composition, Reactions, 2nd ed.; John Wiley: Hoboken, NJ, USA, 1994. [Google Scholar]
  39. Peng, X.X.; Gai, S.; Cheng, K.; Yang, F. Roles of humic substances redox activity on environmental remediation. J. Hazard. Mater. 2022, 435, 129070. [Google Scholar] [CrossRef] [PubMed]
  40. Písaříková, B.; Zralý, Z.; Herzig, I. The effect of dietary sodium humate supplementation on nutrient digestibility in growing pigs. Acta Vet. Brno 2010, 79, 349–353. [Google Scholar] [CrossRef]
  41. Choi, H.; Chen, Y.; Longo, F.; Kim, S.W. Comparative effects of benzoic acid and sodium benzoate in diets for nursery pigs on growth performance and acidification of digesta and urine. J. Anim. Sci. 2023, 101, skad116. [Google Scholar] [CrossRef] [PubMed]
  42. Sauer, W.; Cervantes, M.; Yanez, J.; Araiza, B.; Murdoch, G.; Morales, A.; Zijlstra, R.T. Effect of dietary inclusion of benzoic acid on mineral balance in growing pigs. Livest. Sci. 2009, 122, 162–168. [Google Scholar] [CrossRef]
  43. Kristensen, N.B.; Norgaard, J.V.; Wamberg, S.; Engbaek, M.; Fernandez, J.A.; Zacho, H.D.; Poulsen, H.D. Absorption and metabolism of benzoic acid in growing pigs. J. Anim. Sci. 2009, 87, 2815–2822. [Google Scholar] [CrossRef]
  44. Kluge, H.; Broz, J.; Eder, K. Effect of benzoic acid on growth performance, nutrient digestibility, nitrogen balance, gastrointestinal microflora and parameters of microbial metabolism in piglets. J. Anim. Physiol. Anim. Nutr. 2006, 90, 316–324. [Google Scholar] [CrossRef]
  45. Eriksen, J.; Adamsen, A.P.; Norgaard, J.V.; Poulsen, H.D.; Jensen, B.B.; Petersen, S.O. Emissions of sulfur-containing odorants, ammonia, and methane from pig slurry: Effects of dietary methionine and benzoic acid. J. Environ. Qual. 2010, 39, 1097–1107. [Google Scholar] [CrossRef]
  46. Passi, S.; Nazzaro-Porro, M.; Picardo, M.; Mingrone, G.; Fasella, P. Metabolism of straight saturated medium chain length (C9 to C12) dicarboxylic acids. J. Lipid Res. 1983, 24, 1140–1147. [Google Scholar] [CrossRef] [PubMed]
  47. van Kempen, T.A. Dietary adipic acid reduces ammonia emission from swine excreta. J. Anim. Sci. 2001, 79, 2412–2417. [Google Scholar] [CrossRef] [PubMed]
  48. Zhu, J.; Jacobson, L.D. Correlating microbes to major odorous compounds in swine manure. J. Environ. Qual. 1999, 28, 737–744. [Google Scholar] [CrossRef]
  49. Jensen, M.T.; Cox, R.P.; Jensen, B.B. 3-Methylindole (skatole) and indole production by mixed populations of pig fecal bacteria. Appl. Environ. Microbiol. 1995, 61, 3180–3184. [Google Scholar] [CrossRef] [PubMed]
  50. Lo, S.H.; Chen, C.Y.; Wang, H.T. Three-step in vitro digestion model for evaluating and predicting fecal odor emission from growing pigs with different dietary protein intakes. Anim. Biosci. 2022, 35, 1592–1605. [Google Scholar] [CrossRef] [PubMed]
  51. Niyonsaba, A.; Jin, X.H.; Kim, Y.Y. Effect of reducing dietary crude protein level on growth performance, blood profiles, nutrient digestibility, carcass traits, and odor emissions in growing-finishing pigs. Anim. Biosci. 2023, 36, 1584–1595. [Google Scholar] [CrossRef]
  52. Yang, F.; Tang, C.; Antonietti, M. Natural and artificial humic substances to manage minerals, ions, water, and soil microorganisms. Chem. Soc. Rev. 2021, 50, 6221–6239. [Google Scholar] [CrossRef]
  53. Benz, M.; Schink, B.; Brune, A. Humic acid reduction by propionibacterium freudenreichii and other fermenting bacteria. Appl. Environ. Microbiol. 1998, 64, 4507–4512. [Google Scholar] [CrossRef]
  54. Deng, J.J.; Deng, D.; Wang, Z.L.; Luo, X.C.; Chen, H.P.; Liu, S.Y.; Ma, X.Y.; Li, J.Z. Indole metabolism mechanisms in a new, efficient indole-degrading facultative anaerobe isolate Enterococcus hirae GDIAS-5. J. Hazard. Mater. 2022, 434, 128890. [Google Scholar] [CrossRef]
Table 1. Ingredient composition and chemical composition of experimental diets on an as-is basis.
Table 1. Ingredient composition and chemical composition of experimental diets on an as-is basis.
ItemExperimental Diet
ControlBenzoic AcidAdipic AcidBromelainHumic Substances 1
Ingredients, %
Ground corn68.368.368.368.368.3
Soybean meal, 45.1% crude protein17.017.017.017.017.0
Rapeseed meal10.010.010.010.010.0
Soybean oil1.01.01.01.01.0
L-Lys·HCl, 78.8%0.320.320.320.320.32
L-Thr, 99.0%0.070.070.070.070.07
DL-Met, 99.0%0.020.020.020.020.02
Dicalcium phosphate1.01.01.01.01.0
Ground limestone0.80.80.80.80.8
Salt0.30.30.30.30.3
Vitamin-mineral premix 20.30.30.30.30.3
Corn starch1.0----
Benzoic acid-1.0---
Adipic acid--1.0--
Bromelain---1.0-
Humic substances----1.0
Analyzed chemical composition
Dry matter, %87.587.087.587.587.4
Gross energy, kcal/kg38873907389939003868
Crude protein, %17.417.517.417.518.0
Ash, %5.15.05.05.25.5
Amylase-treated neutral detergent fiber, %10.410.511.19.510.9
Acid detergent fiber, %4.14.24.43.84.2
1 Humic substances contained 55.8% humic acid, 2.7% fulvic acid, and 9.5% potassium oxide, as-is basis. 2 Provided the following quantities per kilogram of complete diet: vitamin A, 18,000 IU; vitamin D3, 3600 IU; vitamin E, 60 IU; vitamin K, 5 mg; thiamin, 5 mg; riboflavin, 8 mg; pyridoxine, 5 mg; vitamin B12, 0.06 mg; pantothenic acid, 30 mg; folic acid, 2 mg; niacin, 30 mg; biotin, 0.30 mg; Co, 0.75 mg as cobalt sulfate; Cu, 60 mg as copper sulfate; Fe, 120 mg as iron sulfate; I, 0.68 mg as calcium iodate; Mn, 60 mg as manganese sulfate; Zn, 60 mg as zinc sulfate.
Table 2. Apparent total tract digestibility (ATTD) of dry matter (DM) and nitrogen (N) balance in pigs fed the experimental diets 1.
Table 2. Apparent total tract digestibility (ATTD) of dry matter (DM) and nitrogen (N) balance in pigs fed the experimental diets 1.
ItemExperimental Diet 2SEMp-Value
ControlBenzoic AcidAdipic AcidBromelainHumic Substances
Dry matter intake, kg/d1.41.41.41.41.40.060.888
N intake, g/d46.546.946.946.549.02.020.124
Fecal DM output, kg/d0.18 bc0.19 ab0.19 bc0.17 c0.21 a0.010.006
ATTD of DM, %88.2 ab87.1 bc87.5 abc88.5 a86.3 c1.010.022
Fecal N output, g/d6.0 b6.4 b6.5 b5.7 b7.9 a0.510.002
ATTD of N, %86.9 a86.2 a86.0 a87.6 a83.7 b1.010.018
Urine output, kg/d2.42.73.03.33.10.360.334
Urinary N output, g/d14.213.317.815.716.22.040.158
Digested N, g/d40.540.540.440.841.02.030.980
Retained N, g/d26.227.222.725.024.81.570.098
N retention, % of ingested56.758.248.354.050.83.590.074
N retention, % of digested65.467.656.461.760.74.020.144
1 Data are least squares means of 6 observations. 2 Each of benzoic acid, adipic acid, bromelain, and humic substances was supplemented to the control diet at 1% at the expense of corn starch. a–c Means within a row without a common superscript letter differ (p < 0.05).
Table 3. Urinary and slurry pH of pigs fed the experimental diets 1.
Table 3. Urinary and slurry pH of pigs fed the experimental diets 1.
ItemExperimental Diet 2SEMp-Value
ControlBenzoic AcidAdipic AcidBromelainHumic Substances
Urinary pH8.61 a7.83 ab7.17 b8.59 a8.67 a0.300.006
Slurry pH8.067.557.257.938.040.310.074
1 Data are least squares means of 6 observations. 2 Each of benzoic acid, adipic acid, bromelain, and humic substances was supplemented to the control diet at 1% at the expense of corn starch. a,b Means within a row without a common superscript letter differ (p < 0.05).
Table 4. Volatile fatty acids (VFA), phenol compounds, and indole compounds in feces and slurry from pigs fed the experimental diets 1.
Table 4. Volatile fatty acids (VFA), phenol compounds, and indole compounds in feces and slurry from pigs fed the experimental diets 1.
Item, mg/LExperimental Diet 2SEMp-Value
ControlBenzoic AcidAdipic AcidBromelainHumic Substances
VFA in feces
Acetate393038683559394336412830.698
Propionate198118071788174217411820.818
Isobutyrate290264247218201290.153
Butyrate109784298494910301160.607
Isovalerate490417407366322430.062
Valerate529402406346361660.139
Phenol compound in feces 3
p-Cresol16.014.520.018.111.73.60.431
Indole compound in feces
Indole5.57.55.13.24.01.40.485
Skatole9.07.310.58.86.82.20.160
VFA in slurry
Acetate126813401220123810031770.727
Propionate387418482344314860.650
Isobutyrate56.757.264.941.835.213.10.445
Butyrate243220261182191530.787
Isovalerate102951157661220.447
Valerate1181011146863290.437
Phenol compound in slurry
Phenol4.54.63.14.73.90.80.512
p-Cresol1551368410978380.209
Indole compound in slurry
Indole1.61.71.20.80.70.40.084
Skatole1.51.01.31.00.80.30.290
1 Data are least squares means of 6 observations. 2 Each of benzoic acid, adipic acid, bromelain, and humic substances was supplemented to the control diet at 1% at the expense of corn starch. 3 Phenol was not detected in the fecal samples.
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Yoo, S.B.; Song, Y.S.; Seo, S.; Kim, B.G. Effects of Supplemental Benzoic Acid, Bromelain, Adipic Acid, and Humic Substances on Nitrogen Utilization, Urine pH, Slurry pH, and Manure Odorous Compounds in Pigs. Animals 2024, 14, 82. https://doi.org/10.3390/ani14010082

AMA Style

Yoo SB, Song YS, Seo S, Kim BG. Effects of Supplemental Benzoic Acid, Bromelain, Adipic Acid, and Humic Substances on Nitrogen Utilization, Urine pH, Slurry pH, and Manure Odorous Compounds in Pigs. Animals. 2024; 14(1):82. https://doi.org/10.3390/ani14010082

Chicago/Turabian Style

Yoo, Seung Bin, Yoon Soo Song, Siyoung Seo, and Beob Gyun Kim. 2024. "Effects of Supplemental Benzoic Acid, Bromelain, Adipic Acid, and Humic Substances on Nitrogen Utilization, Urine pH, Slurry pH, and Manure Odorous Compounds in Pigs" Animals 14, no. 1: 82. https://doi.org/10.3390/ani14010082

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