AU2021103168A4 - A preparation method of high palatability anionic salt for dairy cattle - Google Patents
A preparation method of high palatability anionic salt for dairy cattle Download PDFInfo
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- 241000283690 Bos taurus Species 0.000 title claims abstract description 64
- 125000000129 anionic group Chemical group 0.000 title claims abstract description 35
- 235000019629 palatability Nutrition 0.000 title claims abstract description 30
- 235000013365 dairy product Nutrition 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims abstract description 30
- -1 anion salt Chemical class 0.000 claims abstract description 28
- 239000002994 raw material Substances 0.000 claims abstract description 25
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 235000019764 Soybean Meal Nutrition 0.000 claims abstract description 19
- 239000004455 soybean meal Substances 0.000 claims abstract description 19
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims abstract description 15
- 235000019341 magnesium sulphate Nutrition 0.000 claims abstract description 15
- 150000001413 amino acids Chemical class 0.000 claims abstract description 14
- 235000019270 ammonium chloride Nutrition 0.000 claims abstract description 10
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011777 magnesium Substances 0.000 claims abstract description 7
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 7
- 239000011573 trace mineral Substances 0.000 claims abstract description 5
- 235000013619 trace mineral Nutrition 0.000 claims abstract description 5
- 238000000855 fermentation Methods 0.000 claims description 26
- 230000004151 fermentation Effects 0.000 claims description 26
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 17
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 claims description 17
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 12
- 229920006395 saturated elastomer Polymers 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 8
- 241000193830 Bacillus <bacterium> Species 0.000 claims description 7
- 229920002261 Corn starch Polymers 0.000 claims description 7
- 235000019750 Crude protein Nutrition 0.000 claims description 7
- 108010073771 Soybean Proteins Proteins 0.000 claims description 7
- 239000008120 corn starch Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 235000019710 soybean protein Nutrition 0.000 claims description 7
- 235000014655 lactic acid Nutrition 0.000 claims description 6
- 239000004310 lactic acid Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 240000006439 Aspergillus oryzae Species 0.000 claims description 4
- 235000002247 Aspergillus oryzae Nutrition 0.000 claims description 4
- 241000894006 Bacteria Species 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 235000018102 proteins Nutrition 0.000 claims description 3
- 102000004169 proteins and genes Human genes 0.000 claims description 3
- 108090000623 proteins and genes Proteins 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 108091005804 Peptidases Proteins 0.000 claims description 2
- 239000004365 Protease Substances 0.000 claims description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 230000000536 complexating effect Effects 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 239000011669 selenium Substances 0.000 claims description 2
- 229910052711 selenium Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000011572 manganese Substances 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 229940071440 soy protein isolate Drugs 0.000 claims 1
- 238000012360 testing method Methods 0.000 abstract description 30
- 230000000694 effects Effects 0.000 abstract description 17
- 150000001450 anions Chemical class 0.000 abstract description 3
- 239000000047 product Substances 0.000 description 20
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 18
- 239000011575 calcium Substances 0.000 description 18
- 229910052791 calcium Inorganic materials 0.000 description 18
- 230000009984 peri-natal effect Effects 0.000 description 16
- 238000011282 treatment Methods 0.000 description 12
- 210000002700 urine Anatomy 0.000 description 12
- 235000005911 diet Nutrition 0.000 description 11
- 230000037213 diet Effects 0.000 description 11
- 235000013336 milk Nutrition 0.000 description 9
- 239000008267 milk Substances 0.000 description 9
- 210000004080 milk Anatomy 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 8
- 235000021050 feed intake Nutrition 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 208000013038 Hypocalcemia Diseases 0.000 description 7
- 230000000705 hypocalcaemia Effects 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 206010037660 Pyrexia Diseases 0.000 description 6
- 208000003142 Retained Placenta Diseases 0.000 description 6
- 206010038758 Retained placenta or membranes Diseases 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 201000010099 disease Diseases 0.000 description 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
- 208000030159 metabolic disease Diseases 0.000 description 6
- 206010033799 Paralysis Diseases 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 210000000988 bone and bone Anatomy 0.000 description 4
- 210000002219 extraembryonic membrane Anatomy 0.000 description 4
- 230000006651 lactation Effects 0.000 description 4
- 208000004396 mastitis Diseases 0.000 description 4
- 230000000717 retained effect Effects 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 238000010171 animal model Methods 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 238000007726 management method Methods 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 208000010444 Acidosis Diseases 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 241000511010 Eustoma Species 0.000 description 2
- 241000511730 Leymus chinensis Species 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 230000007950 acidosis Effects 0.000 description 2
- 208000026545 acidosis disease Diseases 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000009395 breeding Methods 0.000 description 2
- 230000001488 breeding effect Effects 0.000 description 2
- 208000016097 disease of metabolism Diseases 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 208000010515 dystocia Diseases 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000002503 metabolic effect Effects 0.000 description 2
- 230000004118 muscle contraction Effects 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000004460 silage Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- GMRQFYUYWCNGIN-ZVUFCXRFSA-N 1,25-dihydroxy vitamin D3 Chemical compound C1([C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@@H](CCCC(C)(C)O)C)=CC=C1C[C@@H](O)C[C@H](O)C1=C GMRQFYUYWCNGIN-ZVUFCXRFSA-N 0.000 description 1
- 206010006294 Breast oedema Diseases 0.000 description 1
- 208000004145 Endometritis Diseases 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 206010017577 Gait disturbance Diseases 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 208000019395 Lactation disease Diseases 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 208000010428 Muscle Weakness Diseases 0.000 description 1
- 206010028372 Muscular weakness Diseases 0.000 description 1
- 201000010183 Papilledema Diseases 0.000 description 1
- 206010033708 Papillitis Diseases 0.000 description 1
- 102100036893 Parathyroid hormone Human genes 0.000 description 1
- 108090000445 Parathyroid hormone Proteins 0.000 description 1
- 208000021129 Postpartum disease Diseases 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 208000036029 Uterine contractions during pregnancy Diseases 0.000 description 1
- 210000003165 abomasum Anatomy 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 235000014590 basal diet Nutrition 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000019658 bitter taste Nutrition 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000009535 clinical urine test Methods 0.000 description 1
- 210000003022 colostrum Anatomy 0.000 description 1
- 235000021277 colostrum Nutrition 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007071 enzymatic hydrolysis Effects 0.000 description 1
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- JWSMTBMIGYJJJM-UHFFFAOYSA-N magnesium;azane Chemical compound N.[Mg+2] JWSMTBMIGYJJJM-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 210000001087 myotubule Anatomy 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 210000002445 nipple Anatomy 0.000 description 1
- 201000002166 optic papillitis Diseases 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 208000015754 perinatal disease Diseases 0.000 description 1
- 210000002826 placenta Anatomy 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/20—Inorganic substances, e.g. oligoelements
- A23K20/24—Compounds of alkaline earth metals, e.g. magnesium
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K10/00—Animal feeding-stuffs
- A23K10/10—Animal feeding-stuffs obtained by microbiological or biochemical processes
- A23K10/12—Animal feeding-stuffs obtained by microbiological or biochemical processes by fermentation of natural products, e.g. of vegetable material, animal waste material or biomass
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/142—Amino acids; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/20—Inorganic substances, e.g. oligoelements
- A23K20/30—Oligoelements
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/10—Feeding-stuffs specially adapted for particular animals for ruminants
- A23K50/15—Feeding-stuffs specially adapted for particular animals for ruminants containing substances which are metabolically converted to proteins, e.g. ammonium salts or urea
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Inorganic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Birds (AREA)
- Sustainable Development (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Physiology (AREA)
- Fodder In General (AREA)
- Feed For Specific Animals (AREA)
Abstract
The invention discloses a preparation method of high palatability dairy
anion salt, which relates to the field of feed, in particular to a
preparation method of high palatability dairy anion salt. It is made
from the following raw materials: 25-30 parts of complex amino acid
magnesium, 25-30 parts of coated magnesium sulfate, 25-30 parts of
coated ammonium chloride, 10-30 parts of fermented soybean meal or
fermented products, and 0.1-0.15 parts of other complex organic trace
elements; The above raw materials were mixed to produce anionic salt
for dairy cattle. The invention solves the problems of low effective
anion content and poor palatability in the anion salt feed existing in
the prior art.
1/1
Palatability test of anionic salt
-e23
. expeence group
19
7-a- control group
1 2 3 4 5 6 7 8 9 10 11 12 13 14 13
Test days
Figure 1
Test on application effect of anionic salt
o . experience group
0 control group
i 3 4 5 6 3 9 10 1 1 1 15 16 1 N
Test days
Figure 2
Description
1/1
Palatability test of anionic salt -e23
. expeence group 19 7-a- control group
1 2 3 4 5 6 7 8 9 10 11 12 13 14 13
Test days
Figure 1
Test on application effect of anionic salt
o . experience group control group
i 3 4 5 6 3 9 10 1 1 1 15 16 1 N Test days
Figure 2
A preparation method of high palatability anionic salt for
dairy cattle
Technical field
The invention relates to the field of feed, in particular to a
preparation method of anion salt with high palatability for dairy
cattle.
Background technology
Milk fever is a common metabolic disease in old and High
yielding cows, which is also known as postpartum paralysis.
Milk fever mostly occurs within 48-72 hours postpartum, the cause is
postpartum hypocalcemia. Calcium is necessary for normal muscle
contraction and plays an important role in nerve impulse conduction.
Lack of calcium can cause gait instability, shaking, muscle weakness
and even unable to stand. Therefore, cows with hypocalcemia may have
a series of postpartum diseases, such as retained placenta,
endometritis, mastitis, postpartum paralysis, Eustoma displacement
and so on. Moreover, cows suffering from milk fever are more prone to
ketemia, mastitis (E.coli caused mastitis), dystocia, Eustoma
torsion, retained placenta and other diseases in the future lactation
season. Perinatal period (generally refers to the period from 21 days
before delivery to 15 days after delivery) is a period of cow
diseases. Because blood calcium is excreted with colostrum, almost
all cows will produce hypocalcemia in the first few days after
production, which will lead to a series of diseases. Calcium is also
a neurotransmitter, affecting the contraction of muscle fibers, so
low calcium causes uterine contraction weakness, resulting in dystocia and retained placenta. In the United States, 8% of cows are clinical and 66% are subclinical. According to statistics, after the occurrence of milk fever, the amount of milk will be reduced by 14%, and the production life will be shortened by 3-4 years. Because of the weakness of nipple muscle contraction, the incidence of papillitis increases. Therefore, hypocalcemia is the root cause of perinatal metabolic disease.
In recent years, China's dairy industry, as an important
industry in the adjustment of agricultural industrial structure, has
developed rapidly. Retained placenta, postpartum paralysis, abomasum
displacement, mastitis and other problems related to calcium
metabolism disorder in late dry milk period have become important
factors restricting further improvement of milk yield. A large number
of studies at home and abroad have shown that feeding anionic salts
to dairy cows during perinatal period can produce subacute metabolic
acidosis in animals. This subacute acidosis can alter the environment
of animal, activate the hormone regulating system of calcium,
strengthen the use of calcium in bone and reabsorb calcium in the
intestine, thus ensuring the high level of calcium in dairy cows'
blood in the specific physiological stage at the perinatal stage,
lowering the incidence rate of post natal diseases, and ensuring the
recovery of the intake of postpartum dairy cows. It is helpful to
improve the milk yield of cows in the next lactation period. Foreign
studies also show that the incidence rate of lactation fever is
related to the level of animal production. The higher the level of
production, the higher the risk of breast fever and other diseases.
The anionic salts of dairy cattle refer to those mineral salts
with relatively high contents of chloride and sulfur ions and
relatively low contents of sodium and potassium. Its main application is to make cows have hypocalcemia symptoms by feeding anionic salt in a certain period of time before delivery. The pH of urine test is
5.5-6.5 (normal is 7-8.5), so that the body can mobilize bone calcium
into the blood reflexively. The mechanism of bone calcium
mobilization can be established before production, so as to avoid
postpartum hypocalcemia and prevent a series of perinatal metabolic
diseases. It has great significance for dairy production. Many
studies have shown that if effective measures are taken to prevent
perinatal diseases, the incidence rate of lactation diseases will be
reduced by 90% (Goff, 1998), and the whole lactation period will also
increase significantly.
However, anionic salts are mainly composed of ammonium, calcium,
magnesium chloride or sulfide monomer or mixture. Most of these salts
have bitter and astringent taste, and the taste of dairy cows is
extremely sensitive. Therefore, anionic salt products face the problem
of poor palatability, that is, dairy cows have the phenomenon of
decreased feed intake and refusal to eat. It is difficult to use and
achieve the expected effect. Therefore, the purpose of the invention
is to develop a kind of anion salt with good palatability and high
utilization rate, so as to provide theoretical basis for controlling
the metabolic disorder related to postpartum hypocalcemia and improving
the milk production performance of dairy cows.
The invention provides a preparation method of cow anion salt with
high palatability, which solves the problems of low effective anion
content and poor palatability in anion salt feed in the prior art.
In order to solve the above problem, the invention adopts the
following technical scheme: a preparation method of cow anion salt with
high palatability
Methods: it was made from the following raw materials: 25-30 parts of
complex amino acid magnesium, 25-30 parts of coated magnesium sulfate,
-30 parts of coated ammonium chloride, 10-30 parts of fermented
soybean meal or fermented products, and 0.1-0.15 parts of other complex
organic trace elements; The above raw materials were mixed to produce
anionic salt for dairy cattle.
The invention has the following advantages: 1. High palatability:
the invention solves the problem of poor palatability of traditional
anion salt products, and has no significant effect on the feed intake
of perinatal cattle; 2. High utilization rate: the invention transforms
part of inorganic salts into organic salts in the form of amino acid
complex through fermentation and enzymatic hydrolysis, so as to improve
the absorption and utilization rate of animal body. To avoid waste and
to protect the environment at the same time; 3. Remarkable effect:
after a large number of experiments, the invention can significantly
solve the metabolic diseases of peripartum dairy cows such as retained
fetal membranes, postpartum paralysis, etc; 4. Easy to use: the anion
salt is organically and coated, which greatly reduces the oxidative
damage of the anion salt to the vitamins in the cow diet. Feed
enterprises and breeding enterprises can be convenient to use.
Illustration
Fig. 1 is the curve diagram of the palatability comparison test results
of anionic salt in embodiment 2 of the invention;
Fig. 2 is the result curve of the contrast test of the use effect of
anionic salt in embodiment 2 of the invention.
Specific implementation mode
The invention is described in detail with the best embodiment.
The preparation method of cow anion salt with high palatability is
made from the following raw materials: 25-30 parts of complex amino
acid magnesium, 25-30 parts of coated magnesium sulfate, 25-30 parts
of coated ammonium chloride, 10-30 parts of fermented soybean meal or
fermented products, and 0.1-0.15 parts of other complex organic trace
elements; The above raw materials were mixed in a mixer for 3 minutes
to prepare the anionic salt of dairy cows. The use stage and object
of the invention are: pre perinatal (21 days before delivery to
delivery) cows. The usage amount of the invention: 150-250g per cow
per day.
The compound amino acid complex magnesium is prepared from raw
materials with the following weight parts ratio: 25-30 parts of
peeled soybean meal containing 46% crude protein, 5-10 parts of
soybean protein isolate and 60-70 parts of magnesium sulfate; Put the
peeled soybean meal, soybean protein isolate and other protein raw
materials into the fermentation tank, sterilize them with 3-4kg
saturated vapor pressure, put in 10 times of the mass of Bacillus,
stir and mix them evenly, then raise the temperature to 30-40 °C and
add protease, put air into the fermentation tank and stir for 18
24hAfter enzymolysis into amino acids, magnesium sulfate was added
for complexing, and the raw materials were taken out of the
fermentation tank for drying after 4-6 hours.
The coating magnesium sulfate is made of raw materials with the
following weight parts ratio: 30-40 parts magnesium sulfate and 60-70
parts corn starch. The preparation method is as follows: put corn
starch into the fermentation tank, sterilize with 3-4kg saturated
vapor pressure, put in 5 times the mass of Saccharomyces cerevisiae
or Saccharomyces cerevisiae, stir and mix evenly, raise the temperature to 26-30 °C, put in magnesium sulfate after 18-24h, continue to stir for 4-6h, and then take the raw materials out of the fermentation tank for drying.
The coated ammonium chloride is made of raw materials with the
following weight parts ratio: 30-40 parts of ammonium chloride and 60
parts of corn starch. The preparation method is as follows: put
corn starch into fermentation tank, sterilize with 3-4kg saturated
vapor pressure, put in 5 times of the mass of Saccharomyces cerevisiae
or Saccharomyces cerevisiae, stir and mix evenly, then raise the
temperature to 26-30 0C, put in ammonium chloride after 18-24h,
continue to stir for 4-6h, and then take the raw materials out of
fermentation tank for drying.
The fermented soybean meal or fermented product is made of raw
materials with the following weight parts ratio: yeast fermented
product 20 parts
There were 20 lactic acid bacteria fermented products, 30 Bacillus
fermented products and 30 Aspergillus oryzae Fermented Products.
The yeast fermented product is made from the following raw
materials: 95-99 parts of peeled soybean meal containing 46% crude
protein and 1-5 parts of soybean protein isolate; The preparation
method is as follows: smash the peeled soybean meal with 0.5mm sieve
piece, put it into the fermentation tank, sterilize it with 3-4kg
saturated vapor pressure, and put in 8 times of the weight of
Saccharomyces cerevisiae or Saccharomyces cerevisiae liquid (4X109-6
X109 CFU / ml). After mixing, the temperature was controlled to 26
0 C, and the fermentation was stirred. After 18-24 hours, it was out
of the tank and dried.
The lactic acid bacteria fermented product is made from the
following raw materials: 95-99 parts of peeled soybean meal containing
46% crude protein and 1-5 parts of soybean protein isolate; The
preparation method is as follows: use 0.5mm sieve to crush the peeled
soybean meal, put it into the fermentation tank, use 3-4kg saturated
vapor pressure to sterilize with material, and put in 8 times of the
weight of lactic acid bacteria liquid (6X109-8X109 CFU / ml), the
temperature was controlled at 33-37 0C, the fermentation was stirred,
and the fermentation was carried out after 18-24 hours.
The fermented products were made from the following raw materials:
-99 parts of peeled soybean meal containing 46% crude protein and 1
parts of soybean protein isolate; The preparation method is as
follows: use 0.5mm sieve pieces to crush the peeled soybean meal, put
it into the fermentation tank, use 3-4kg saturated vapor pressure to
carry material for sterilization, and put 10 times weight of Bacillus
broth (1.5kg)X1010-2X1010 CFU / ml), the temperature was controlled
at 33-37 0C, the fermentation was stirred, and the fermentation was
carried out after 18-24 hours.
The fermented products of Aspergillus oryzae were made from the
following raw materials: 95-99 parts of peeled soybean meal
containing 46% crude protein and 1-5 parts of soybean protein
isolate; The preparation method is as follows: use 0.5mm sieve to
crush peeled soybean meal, put it into solid fermentation tank, use
3-4kg saturated vapor pressure to carry material for steriization,
and put in twice weight Aspergillus oryzae liquid (spore number: 5)X
106-1XThe temperature was controlled at 30-35 0C, and the
fermentation was stirred. After 18-24 hours, it was out of the tank
and dried.
The other compound organic trace elements are prepared from the
following raw materials in weight parts ratio: selenium enriched
yeast
2-5 The results showed that there were 25-30 parts of complex amino
acid complex zinc, 10-15 parts of complex amino acid complex iron,
-25 parts of complex amino acid complex manganese, 10-15 parts of
complex amino acid complex copper and 15-35 parts of carrier.
Example 1: optimum component ratio test
Test purpose: through comparative test, the optimal ratio of amino
acid complex magnesium, coated magnesium sulfate, coated ammonium
chloride, fermented soybean meal or yeast, bacillus and lactic acid
fermentation material in each component of the invention is selected.
At the same time, the effect of adding the invention on the palatability
of dairy cows and the pH value of urine of dairy cows is evaluated.
Experimental animals: 60 cows were randomly selected in the early
perinatal period (21 days before delivery to delivery), and were
divided into four groups according to the principle of similar
weight, parity and expected delivery date, which were divided into
three treatment groups and a control group, with 15 cows in each
group.
Experimental treatment: the basic diets of four groups were: corn
silage (wet weight) 13kg / head • day, Leymus chinensis 4kg /
head • day;5 kg / head per day. The nutrient concentration of basal
diet: crude protein 14.3%, calcium 0.82%, total phosphorus 0.38%,
ndf4l.2%, adf25.1%.In addition to the basic diet, the three
experimental groups were supplemented with 200 g of compound anionic
salt per head per day. The anionic salt components in each group were different. The proportion of each anionic salt component in the three treatment groups was as follows: project Amino acid Coated Coated Fermented soybean In accordance complex magnesium ammonium meal or with amino magnesium sulfate chloride combination of acid complex yeast, bacillus trace and lactic acid elements fermentation products Treatment 25 25 25 24.85 0.15 group 1 Treatment 27.5 27.5 27.5 17.35 0.15 group 2 Treatment 30 30 30 9.85 0.15 group 3
The results of feed intake and urine pH value were as follows:
Treatment Treatment Treatment control group 1 group 2 group 3 group Average feed 21.82 21.71 21.69 21.73 intake (kg)
Average urine pH of dairy 6.55 6.50 6.35 7.85 cows
The results showed that there was no significant difference in feed
intake between the three treatment groups and the control group, but
there was significant difference in the regulation of urine pH between
group 3 and other groups, and the effect was the best.
Example 2
Objective: To compare the palatability difference between the anionic
salt of the invention and the traditional anionic salt and its use
effect.
Experimental animals and grouping: 80 cows were randomly divided
into experimental group and control group according to the principle of similar weight, parity and expected delivery time, with 40 cows in each group.
Test treatment: this test consists of two tests, one is the
palatability comparison test of two kinds of anionic salts, the other
is the use effect comparison test of two kinds of anionic salts.
Test method: two kinds of anion salt palatability comparative test:
the experimental group and the control group have the same basic diet,
the control group is added with traditional anion salt, and the
experimental group is added with the anion salt of the invention. In
the two treatments, the addition amount of anionic salt increased
gradually, the first day of the experiment was 150 g per cow per day,
increased by 10 g per day, and the maximum addition amount was 250 G.
The feed intake and the amount of surplus feed were recorded.
Comparative test on the use effect of two anionic salts: the basic
diet of the experimental group and the control group was the same, the
traditional anionic salt was added to the control group, and the
anionic salt of the invention was added to the experimental group. The
addition amount was 200g per cow per day. The urine pH value was
recorded.
Annex: basic diet composition: corn silage (wet weight): 12kg / head
/ day; Leymus chinensis: 3.5kg/head per day; Alfalfa: 1kg / head /
day; 5 kg per head per day. The nutrient concentration of basal diet:
crude protein 14.8%; Calcium: 0.84%; Total phosphorus: 0.4%; NDF
40.3% ; ADF : 24.6%.
Feeding management: according to the daily feeding management
standard of the ranch, the total mixed ration (TMR) was fed twice a
day.
Test results and analysis:
1. Comparative test on palatability of two kinds of anionic salt:
the results of comparative test on palatability of anionic salt are
shown in Fig. 1. After the addition of anionic salt, the feed intake
of the control group, that is, the perinatal cattle fed with the
traditional anionic salt diet, began to be affected. When the
addition of anionic salt reached 220g / head • day, the feed intake
decreased rapidly. When the addition of anionic salt reached 250G
/ head • day, The feed intake of dairy cows decreased significantly,
and some dairy cows refused to eat. The feed intake of the cattle in
the experimental group has no obvious change during the whole
experimental period, indicating that the product of the invention
has well solved the problem of palatability of anionic salt.
2Comparative test on the use effect of two kinds of anionic
salts: the results of comparative test on the use effect of
anionic salts are shown in Figure 2. During the whole test
period of the control group, the pH value of cow urine slightly
decreased, but it did not reach the degree of acidity, so the
use effect was general. In the experimental group, the average
urine pH value of the cattle decreased to about 6.5 after one
week of experiment, and the average urine pH value of the
cattle maintained at about 6 after 10 days of continuous
feeding, so as to achieve the purpose of adjustment, which
indicates that the product of the invention is effective.
Example 3
Objective: to test the effect of the product of the invention on
the decline of urine pH value of perinatal cows and the control effect
on the retention rate of fetal membranes.
Experimental animals: the whole dairy farm was selected as the
experimental group, and the control group was empty. The data of the
control group were the historical rate of retained fetal membranes and
midwifery rate. The experiment lasted for 8 months, and the data of
the control group were the average of 5, 6 and 7 months.
Test method: the perinatal cattle of the ranch were from 21 days
before delivery to delivery. The anionic salt of the invention was
added to the diet, the addition amount was 175g / head • day, and the
calcium content in the diet was adjusted to 0.82%. The other feeding
and management methods were the same as the original methods. The urine
pH value of the perinatal cows was continuously measured from 5 days
before the experiment until the delivery. The experimental period was
days, and the data of retained fetal membranes in the first 5 days
of the experiment were not recorded as the experimental data. As the
cattle farm is non centralized breeding, some perinatal cattle will be
transferred to this group continuously during the experimental period.
The delivery data of these cattle during the experimental period (from
the beginning of the experiment to the 60th day of the experiment)
will be recorded into the experimental group data.
Test results and analysis: the following table shows the test
results of the use effect of anionic salts
project PH value of cow Rate of retained Midwifery urine placenta rate Experimental 6.32 8.9% 21.4% group History 7.85 32.5% 37.8%
Improvement From alkalinity to 23.6% reduction 16.4% degree acidity reduction
Results as shown in the table above, the pH value of cow urine was
acidic after adding the product to the diet of perinatal cattle, which
could promote the synthesis and secretion of 1,25-dihydroxyvitamin D and parathyroid hormone PTH, and induce the body to use bone calcium to supplement the loss of blood calcium. The rate of retained placenta and midwifery rate were significantly reduced.
Application effect of feed test
5% (mass percentage) of the product of the invention is added to
% of the concentrated feed of perinatal dairy cows, and the
recommended feeding amount of the concentrated feed is 3-3.5kg per cow
per day, which is equivalent to 165g-192.5g per cow per day. The use
of the product can effectively prevent perinatal metabolic diseases
such as retained placenta, breast edema and postpartum paralysis.
Finally, it should be noted that it is obvious that the above
mentioned embodiments are only examples to clearly illustrate the
present invention, and are not limitations on the embodiments. For
those skilled in the art, other changes or changes in different forms
can be made on the basis of the above description. It is unnecessary
and impossible to enumerate all the implementation methods here. And
the obvious changes or changes thus derived are still within the
protection scope of the present invention.
Claims (6)
1.The invention relates to a preparation method of cow anion salt with
high palatability, which is characterized in that it is made of raw
materials with the following weight parts ratio: compound amino acid
complex magnesium 25-30 parts, coated magnesium sulfate 25-30 parts,
coated ammonium chloride 25-30 parts, fermented soybean meal or hair
powder
-30 parts of fermented products and 0.1-0.15 parts of other complex
organic trace elements; The above raw materials were mixed to produce
anionic salt for dairy cattle.
2. The method for preparing cow anion salt with high palatability
according to claim 1, which is characterized in that the compound salt
The amino acid complex magnesium is prepared from raw materials with
the following weight fraction: peeled soybean meal 25-30 with 46% crude
protein mass fraction
-10 parts of soy protein isolate and 60-70 parts of magnesium sulfate;
The peeled soybean meal and soybean protein isolate were put into the
fermentation tank to make the fermentation time stable
Sterilize with 3-4kg saturated vapor pressure belt, put in 10 times of
the mass of Bacillus, stir and mix evenly, and then raise the
temperature to a minimum
-4OThen, add protease, air into the fermentor and stir for 18-24
hours. After the protein raw materials in the fermentor are fermented
and enzymolyzed into amino acids, put in magnesium sulfate for
complexing. After 4-6 hours, take the raw materials out of the
fermentor and dry them.
3. The preparation method of cow anion salt with high palatability
according to claim 1, which is characterized in that the coating
Magnesium sulfate is made from the following raw materials: magnesium
sulfate 30-40 parts, corn starch 60-70 parts; The preparation method
is as follows
Next: put corn starch into the fermentation tank, sterilize with 3-4kg
saturated vapor pressure, put in 5 times the mass of Saccharomyces
cerevisiae or Saccharomyces cerevisiae liquid, stir and mix evenly,
raise the temperature to 26-30 0C, put in magnesium sulfate after 18
24h, continue to stir for 4-6h, and then take the raw materials out of
the fermentation tank for drying.
4. The preparation method of cow anion salt with high palatability
according to claim 1, which is characterized in that the coating
Ammonium chloride is made from the following raw materials: 30-40 parts
of ammonium chloride and 60-70 parts of corn starch; The preparation
method is as follows
Next: put corn starch into the fermentation tank, sterilize with 3-4kg
saturated vapor pressure, put in 5 times the mass of Saccharomyces
cerevisiae or Saccharomyces cerevisiae, stir and mix evenly, raise the
temperature to 26-30 0C, put in ammonium chloride after 18-24h,
continue to stir for 4-6h, and then take the raw materials out of the
fermentation tank for drying.
5. The method for preparing cow anion salt with high palatability
according to claim 1, which is characterized in that the fermented
soybean meal or fermented product is composed of one or more of yeast
fermented product, lactic acid bacteria fermented product, Bacillus
fermented product and Aspergillus oryzae Fermented Product.
6. The method for preparing cow anion salt with high palatability
according to claim 1, which is characterized in that
The compound organic trace element is made from the following raw
materials: selenium enriched yeast 2-5 parts, complex amino acid
complex zinc
-30The results showed that there were 10-15 parts of complex amino
acid complex iron, 20-25 parts of complex amino acid complex manganese
and 10-15 parts of complex amino acid complex copper
-15 There were 15-35 carriers.
Figure 1 1/1
Figure 2
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