|
Organic Acids Defined
_______________________________________________________________________________
Organic acids (OA) are molecules containing a
carbon chain [R-] and a terminal carboxyl group [COOH]. By contrast, inorganic
acids such as hydrochloric, sulfuric and phosphoric, do not contain carbon in
their chemical structure. The most common OAs used world-wide in livestock diets
are supplied either in a liquid (formic, acetic, propionic, butyric and lactic
acids) or a dry (fumaric, citric, benzoic, and sorbic acids) form, or in the
form of their Ca, Na, K, or ammonium salts. Additionally, the liquid acids may
be adsorbed onto a carrier resulting in a maximum of 60 - 70% of the liquid acid
in the final product. The OA differ in the following ways: 1) their acid
strength (ability to lower pH), 2) solubility in water, 3) molecular weight, 4)
energy content, 5) pKa or pH at which 50% of the acid molecules are in the
dissociated form, and 6) antimicrobial activity.
Functional Role of
Organic Acids
_______________________________________________________________________________
Lactic, formic, propionic, and butyric are among
the OA naturally produced in the gastrointestinal tract (GIT) as a result of
microbial fermentation. Their relative levels vary depending on location
(stomach, small intestine, large intestine) and diet composition (dietary
lactose level, fiber level, etc). Lactic acid is in the greatest concentration
in the stomach and small intestine while another OA, acetic, along with
propionic and butyric are predominant in the large intestine. The main roles of
OA in the GIT are to: 1) increase effectiveness of the barrier function of the
stomach against pathogens by helping to reduce stomach pH, particularly in young
animals, 2) regulate intestinal cell proliferation through direct provision of
energy, altering blood flow and therefore nutrient delivery to intestinal
tissue, and mediation of various gastrointestinal hormones and growth factors
which affect intestinal cell proliferation, 3) increase pancreatic secretions,
4) diffuse across cell membranes of pathogens in the intestine and either
destroy the pathogens cytoplasm or interfere with cellular metabolism of the
pathogen, and 5) serve as a precursor for synthesis of non-essential amino
acids, DNA, and some lipids required for intestinal growth. With these
functional roles, OA are clearly gut environment modifiers (GEMs). OA are also
widely used to improve food, feed, and water hygiene as well as preserve
silages.
Factors Affecting OA
Response
_______________________________________________________________________________
The response to OA can be affected by: 1) type and
level of OA fed, 2) type of diet and its buffering capacity (BC), 3) pig age, 4)
presence/absence of receptors for bacterial colonization on the intestinal
epithelium, 5) influence of maternal antibody protection, 6) hygiene and
environmental factors, and 7) endogenous production of OA as a result of
microbial fermentation of feedstuffs. The performance response to OA is
anticipated to be lower when good hygiene practices are in place and when the
pigs environment such as temperature, humidity and ventilation are nearer to
optimum. Pig genetic lines lacking intestinal receptors for pathogens such as
those exhibiting the Type I fimbria (E. coli for instance) are likely to
see less of a response to OA supplementation. Pigs from farms implementing sow
vaccination for enteric pathogens resulting in elevated levels of maternal
antibody protection at weaning are also likely to see a lower response to OA.
The response to OA is typically best in newly weaned pigs due to immature acid
secreting capacity, and therefore a compromised stomach barrier function. In the
U. S., pigs are typically weaned to high protein diets (20 - 24%) sometimes
containing milk protein from whey, animal protein including but not limited to
plasma, fishmeal, and pet-food grade poultry by-product meal resulting in high
dietary Ca levels (0.9 - 1.0%). Pharmacological levels of Zn (2,500 - 3,000 ppm)
and copper (175 - 250 ppm) are also fed. These factors all contribute to a high
BC of the diet. The high BC of the weaner diet is compounded by the normally low
acid secretory capacity of the weaned pig. Therefore, adequate levels of OA are
needed to decrease the stomach pH sufficiently to provide a barrier function
against pathogens finding their way to the small intestine. Weaner diets are
also composed of more complex protein sources than the dam's milk. Therefore, OA
induced stimulation of pancreatic enzyme secretion should increase piglet growth
and feed utilization efficiency.
Alimet as an OA
_______________________________________________________________________________
ALIMET® feed supplement (DL - 2 Hydroxy-4-(MethylThio)-Butanoic acid, aka HMTBa)
is generally accepted as a methionine source but has the dual functionality of
being structurally similar to lactic acid. In culture
broth studies, ALIMET has been found to have antibacterial properties
against E. coli, Salmonella spp and Campylobacter spp. In
in vitro studies, ALIMET alone at 0.5% has been shown to lead to a reduction in
levels of Salmonella enteritidis similar to that observed with 0.5%
formic acid. ALIMET at 0.25% or 0.375% in combination with 0.25% or 0.125%
formic respectively appeared to act synergistically with respect to Salmonella
kill. This apparent synergy on Salmonella kill between ALIMET and other OA has
also been demonstrated. The mode of action of this synergy is as yet undefined.
Historical Response to
OA
_______________________________________________________________________________
Partanen (2001) summarized numerous (36) trials
where various OA (formic, fumaric, citric and potassium diformate) at varying
levels (0.3 - 2.5%) were fed to weaned pigs. Overall, OA addition improved gain
7.6% and feed efficiency 3.2%. The response was greatest for formic acid and its
salt potassium diformate (11.2% improvement in ADG - Average Daily Gain - and
2.8% improvement in feed conversion). Jongbloed and Jongbloed (1996) evaluated
levels of lactic acid ranging from 0.8% to 3.2% and observed and improvement in
growth rate of 8.3 - 10.2% (avg 9.1%) and feed efficiency of 3.6 - 8.4% (avg
5.6%). Maribo (1999) saw somewhat lower response to 2% lactic acid for two weeks
followed by 1% for two additional weeks observing an improvement of 5.5% in ADG
and 2.8% in feed efficiency. Average improvements in ADG of 16.7% and 18.2% have
been observed by Maribo and Callesen (1998) and Van der Ploeg (1998)
respectively. From these historical data, depending on the factors affecting OA
response, an improvement in gain of 5 - 10% and an improvement in feed
conversion of 2 - 5% may be anticipated.
Activate Starter DA and
Associated Performance
_______________________________________________________________________________
ACTIVATE STARTER DA®
is a blend of ALIMET, benzoic, and fumaric acids formulated to enhance stomach
barrier function against pathogenic bacteria such as E. coli and
Salmonella. By reducing the intestinal damage associated with these pathogens,
and by the other functional properties outlined above, a performance enhancement
when included at 0.5% in weaning pig diets is anticipated. Results of ten trials
confirm a 5.1% improvement in ADG and a 3.2% improvement in feed conversion when
ACTIVATE STARTER DA is added to non-medicated diets for approximately 40 days.
Furthermore, an ACTIVATE STARTER DA program through 40-d post-weaning achieved
87% of the ADG response and 107% of the feed efficiency response of a Carbadox
medication program. These results confirm the effectiveness of ACTIVATE STARTER
DA as a means of weaning pig performance.
NOTICE: While the information contained herein (“Information”) is presented in
good faith and believed to be correct as of the date hereof, Novus
International, Inc. does not guarantee satisfactory results from reliance upon
such Information, disclaims all liability for any loss or damage arising out of
any use of this Information or the products to which said Information refers and
MAKES NO REPRESENTATIONS OR WARRANTIES, EITHER EXPRESS OR IMPLIED, OF
MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE OR OF ANY OTHER NATURE WITH
RESPECT TO THE INFORMATION OR PRODUCTS, except as set forth in Novus’ standard
conditions of sale. Nothing contained herein is to be construed as a
recommendation to use any product or process in conflict with any patent, and
Novus International, Inc. makes no representation or warranty, express or
implied, that the use thereof will not infringe any patent.
®
ALIMET, ACTIVATE and NOVUS are trademarks of Novus International, Inc. and is
registered in the Unites States and other countries.
TM
GEM-LINE is a trademark of Novus International, Inc.
©
2007 Novus International, Inc.
GL001S_012407 Effective 02/09/07
|