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Sheep digestion

Leroy and Michaux found that sheep digested a high proportion of the pectic substances included in such foodstuffs as apple pulp, sugar beet pulp, hay, and straw. It was found that a sheep feeding on hay consumed from 75 to 102 g. daily of pectic substances (Michaux). The proportion of pectic acid to pectin is high in apple and sugar beet pulp, the ratio being... [Pg.144]

Acetamide has been used experimentally as a source of nonprotein nitrogen for sheep and dairy cattie (13). It does not appear to be toxic in amounts of about 2—3% of ration. Buffering the diet with dibasic acids serves to allow higher levels of intake because the ammonia Hberated in the digestive process is then scavenged. [Pg.73]

Cobalt is one of twenty-seven known elements essential to humans (28) (see Mineral NUTRIENTS). It is an integral part of the cyanocobalamin [68-19-9] molecule, ie, vitamin B 2> only documented biochemically active cobalt component in humans (29,30) (see Vitamins, VITAMIN Vitamin B 2 is not synthesized by animals or higher plants, rather the primary source is bacterial flora in the digestive system of sheep and cattle (8). Except for humans, nonmminants do not appear to requite cobalt. Humans have between 2 and 5 mg of vitamin B22, and deficiency results in the development of pernicious anemia. The wasting disease in sheep and cattle is known as bush sickness in New Zealand, salt sickness in Florida, pine sickness in Scotland, and coast disease in AustraUa. These are essentially the same symptomatically, and are caused by cobalt deficiency. Symptoms include initial lack of appetite followed by scaliness of skin, lack of coordination, loss of flesh, pale mucous membranes, and retarded growth. The total laboratory synthesis of vitamin B 2 was completed in 65—70 steps over a period of eleven years (31). The complex stmcture was reported by Dorothy Crowfoot-Hodgkin in 1961 (32) for which she was awarded a Nobel prize in 1964. [Pg.379]

The ability to identify and quantify cyanobacterial toxins in animal and human clinical material following (suspected) intoxications or illnesses associated with contact with toxic cyanobacteria is an increasing requirement. The recoveries of anatoxin-a from animal stomach material and of microcystins from sheep rumen contents are relatively straightforward. However, the recovery of microcystin from liver and tissue samples cannot be expected to be complete without the application of proteolytic digestion and extraction procedures. This is likely because microcystins bind covalently to a cysteine residue in protein phosphatase. Unless an effective procedure is applied for the extraction of covalently bound microcystins (and nodiilarins), then a negative result in analysis cannot be taken to indicate the absence of toxins in clinical specimens. Furthermore, any positive result may be an underestimate of the true amount of microcystin in the material and would only represent free toxin, not bound to the protein phosphatases. Optimized procedures for the extraction of bound microcystins and nodiilarins from organ and tissue samples are needed. [Pg.120]

Although /3-oxidation is universally important, there are some instances in which it cannot operate effectively. For example, branched-chain fatty acids with alkyl branches at odd-numbered carbons are not effective substrates for /3-oxidation. For such species, a-oxidation is a useful alternative. Consider phy-tol, a breakdown product of chlorophyll that occurs in the fat of ruminant animals such as sheep and cows and also in dairy products. Ruminants oxidize phytol to phytanic acid, and digestion of phytanic acid in dairy products is thus an important dietary consideration for humans. The methyl group at C-3 will block /3-oxidation, but, as shown in Figure 24.26, phytanic acid a-hydroxylase places an —OFI group at the a-carbon, and phytanic acid a-oxidase decar-boxylates it to yield pristanie add. The CoA ester of this metabolite can undergo /3-oxidation in the normal manner. The terminal product, isobutyryl-CoA, can be sent into the TCA cycle by conversion to succinyl-CoA. [Pg.796]

KLITA P T, MATHISON G w, FENTON T w, HARDIN R T (1996) Effects of alfalfa root saponins on digestive function in sheep. JAnim Sci. 74 1144-56. [Pg.180]

Mansion, R. Gleed, P. T. (1985). Reaction cements as materials for the sustained release of trace elements into the digestive tract of cattle and sheep. II. Release of cobalt and selenium. Journal of Veterinary Pharmacology Therapeutics, 8, 374-81. [Pg.273]

Waghom GC, Stafford KJ. Gas production and nitrogen digestion by rumen microbes from deer and sheep. New Zealand Journal Agricultural Research. 1993 36 493-497. [Pg.257]

Significantly enhanced growth when compared to sheep fed 0.36 mg Mo/kg diet growth associated with increased cellulose digestibility by rumen biota (5)... [Pg.1566]

When planning for Tilley and Terry digestibilities, it is common practice to ensure that the sheep or cattle have been fed for a couple of weeks on a basal diet similar to the test samples to be analysed. This is to ensure a buildup of the appropriate rumen flora resulting in a corresponding optimal activity. Whether or not this is necessary is open to question, and this and other sources of error have been discussed by Ayres (1991). It is also customary not to feed the animal on the morning planned for extracting the rumen liquor. [Pg.46]

Blaxter, K.L., Graham, N.Mc. and Wainman, F.W. (1956) Some observations on the digestibility of food by sheep and on related problems. British Journal of Nutrition 10, 59-91. [Pg.208]

Humans do not produce the enzymes, called cellulases, necessary to digest cellulose. Bacteria possessing cellulase inhabit the digestive tracts of animals such as sheep, goats, and cows giving these animals the ability to digest cellulose. Cellulase bacteria also exist in the digestive systems of... [Pg.223]


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See also in sourсe #XX -- [ Pg.159 ]




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Sheep, digestive process

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