Use of phytase and citric acid supplementation on growth performance and nutrient digestibility of Cirrhinus mrigala fingerlings fed on canola meal based diet

Fishmeal; being a limited and costly feed ingredient is continuously been substituted with locally available plant proteins. However, the occurrence of anti-nutritional factors in plant meal suppresses its potential to be fully replaced. Therefore, in this study we aimed to study the synergistic effects of dietary additives like citric acid and phytase enzyme supplementation on growth performance and nutrient digestibility of Cirrhinus mrigala fingerlings. Canola meal (CM) was used as a test ingredient to replace fishmeal (FM) as; 0%, 25%, 50% and 75%. These four diets were further supplemented by varying levels of phytase (0 and 750 FTU kg-1) and citric acid (0% and 2.5%) to formulate total sixteen test diets as T1, T2, T3, T4, T5, T6, T7, T8, T9, T10, T11, T12, T13, T14, T15 and T16. Each treatment contained three replicates; applied to fish groups having 15 fingerlings each; following 3×3 factorial arrangement. 1% of chromic oxide was added as an inert marker. Maximum weight gain% (288%) and the lowest value of FCR (1.07) were recorded when fish was fed on diet T12 as compared to fish fed control diet (T1). Similarly, optimum nutrient digestibility values such as crude protein (77%), crude fat (84%) and gross energy (70%) were noted on same level. It was concluded that 50% canola meal can optimally replace fishmeal when supplemented with phytase and citric acid at the levels of 750 FTU kg-1 and 2.5%, respectively.

Fermentation of liquid feed with lactic acid bacteria reduces dry matter losses, lysine breakdown, formation of biogenic amines and phytate-phosphorus

ABSTACT This study investigated the fermentation of liquid feed for pigs and the effect of lactic acid bacteria (LAB) supplementation on fermentation rate, dry matter losses (DML), formation of biogenic amines and degradation of phytate-P. The basal substrate in all three in-vitro batch experiments consisted of 50% canola meal, 25% wheat, and 25% barley. The mixed substrates were adjusted to a dry matter (DM) content of 28.4% and fermented in 1L-vessels at 37° C for 24 h. Experiment 1 focused on changes in pH profiles over time. Treatments were: (1) liquid feed without additive (control) and (2) liquid feed supplemented with a mixture of Lactobacillus plantarum, Pediococcus pentosaceus, and Lactobacillus lactis (adLAB) at 2.0 × 10 5 CFU/g liquid feed (wet wt.; n = 8). Substrate pH was measured every 2 h. Experiment 2 focused on DML and the impact of fermentation on phytate-P. Treatments were identical to experiment 1 (control and adLAB; n = 8). Measured parameters included concentration of lactic acid, acetic acid, ethanol, and phytate-P, and DML after 24 h of fermentation. Counts of molds, Enterobobacteriaceae, yeasts and LAB were determined in one combined sample of all replicates. Dry matter losses were lower in LAB supplemented fermentations (5.89%) compared to the control (11.8%; P < 0.001). Supplementation with LAB reduced the phytate-P content (2.66 g/kg DM) compared to the control (3.07 g/kg DM; P = 0.002). Experiment 3 evaluated DML and the impact of fermentation on formation of biogenic amines. Treatments were: (1) control, (2) adLAB (2.0 × 10 5 CFU LAB/g liquid feed), (3) adLys (0.60% DM supplemented lysine) and (4) adLAB+Lys (combination of adLAB and adLys; n = 8). The fermentation of adLys resulted in a nearly complete breakdown of supplemented lysine, while only 10% of supplemented lysine was lost in adLAB+Lys. Furthermore, all adLys samples tested positive for cadaverine (mean concentration 0.89% DM), while no adLAB samples contained cadaverine above the detection limit (P < 0.001). Results indicate that DML is reduced in fermentations supplemented with homofermentative LAB. Fermentation of liquid feed with homofermentative LAB can effectively reduce the degradation of supplemental lysine, and has the potential to further improve P availability.

Mulberry leaves as a feed source for livestock in Kenya: A Review

In Kenya, Mulberry is grown in less than a piece of an acre by most of the farmers. Current acreage of mulberry stands at 250, spread over Western, Nyanza, and Rift Valley and Coastal regions. Mulberry leaves are highly palatable and digestible (70-90%) to ruminants and can be fed to non-ruminants as part of feed ingredient. Protein content and essential amino acid profile in the leaves and young stems varies from 15 to 35% depending on the variety. The Mulberry leaves are highly applicable as supplements replacing concentrates for dairy cattle, as the main feed for goats and sheep, and as an ingredient in rabbits and pigs’ diets. Farmers growing mulberry fodder offer higher protein content to livestock than those relying on different varieties of Napier grass, which have failed to boost milk production despite the amounts fed. In non-ruminant production, fishmeal and soybean meals are the main source of protein. In ruminant production, cottonseed meal and canola meal are the main source of protein. These meals are expensive, inadequate in supply and of variable quality. This often leads to low egg production and poor-quality eggs, hence low income and poverty among farmers. Therefore, efforts have been made to identify locally available protein feed resources that can be used as a protein supplement for livestock. Mulberry leaf meal (MLM) has been identified as a locally available alternative protein and mineral source that are beneficial to livestock and have been proven to improve production. Int. J. Agril. Res. Innov. Tech. 11(2): 1-9, Dec 2021

Breeding Canola (Brassica napus L.) for Protein in Feed and Food

Interest in canola (Brassica napus L.) ­In response to this interest, scientists have been tasked with altering and optimizing the protein production chain to ensure canola proteins are safe for consumption and economical to produce. Specifically, the role of plant breeders in developing suitable varieties with the necessary protein profiles is crucial to this interdisciplinary endeavour. In this article, we aim to provide an overarching review of the canola protein chain from the perspective of a plant breeder, spanning from the genetic regulation of seed storage proteins in the crop to advancements of novel breeding technologies and their application in improving protein quality in canola. A review on the current uses of canola meal in animal husbandry is presented to underscore potential limitations for the consumption of canola meal in mammals. General discussions on the allergenic potential of canola proteins and the regulation of novel food products are provided to highlight some of the challenges that will be encountered on the road to commercialization and general acceptance of canola protein as a dietary protein source.

PSXIII-12 Exploring nutritional differences of canola seeds and bio-processing co-products (meals, pellets) from different processing plants/companies in Canada and China for dairy cattle

Canola was created as a low erucic acid and low glucosinolate seed, to produce high quality oil for human consumption and meal for use in livestock feed. China is an important user of Canadian canola products (seeds, oil, and meal). The extraction of the oil from the seed produces a co-product called canola meal. This meal is rich in protein and is used as a protein source in animal diets. However, differences in the characteristics of the seeds, or processing methods during oil extraction may affect the quality of this co-product. Plus, the synthesis of tissues and milk is related to the amino acids available to the animal for absorption in the small intestine. This study aimed to determine if there are significant differences in the intestinal digestibility (in vitro) of CP and DM between canola seeds and meals from different companies in Canada and to determine if there are significant differences between them in Canada and China. The three-step procedure was applied on residues from a 12-hour rumen incubation in fistulated dairy cows to estimate the intestinal digestibility of CP and DM. There were significant differences (P < 0.05) for TDDM (Total digestible dry matter) and IDP (intestinal digestibility of protein) of the meals between countries. The samples from China had higher TDDM (83.76% versus 81.53%, P = 0.018), while Canada’s had higher IDP (68.51% versus 65.28%, P = 0.016). No significant differences were observed within countries. Based on the material analyzed during this study, it is safe to affirm that there are no significant differences in the digestibility of DM and CP between Canada and China. It was concluded that the quality of the canola seeds or meals produced in both Canada and China were similar when used in dairy rations. Key words: canola seeds and bio-processing co-products (meals, pellets), nutritional differences, dairy cows

307 Effect of Feeding Distilllers Grain from Wheat on Growth Performance of Growing and Finishing Beef Cattle

The uniqueness of wheat-based distiller grain (wDG) with high protein and digestible fibre gives great feeding opportunities for cattle as energy, protein or fiber source. This abstract summarizes recent research findings on the use of wDG in beef cattle diets. For growing beef cattle, steers fed diets (forage:concentrate, 55:45) with increasing replacement of barley grain with wDG from 0, 8, 16, 24 to 32% (DM basis) linearly (P < 0.01) increased average daily gain (ADG) from 1.09 to 1.28 kg/d and DM intake (DMI) from 7.26 to 7.94 kg/d without affecting gain:feed (0.158). By comparing protein source of canola meal and corn DG in diets containing 60% of silage and 40% of barley grain, steers fed wDG diet had similar ADG (1.46 kg/d) with corn DG (1.51 kg/d), and had no differences in gain:feed (0.178) with canola meal (0.183). For finishing beef cattle, with increasing wDG from 10, 20 to 40% in the place of barley grain of finishing diets, the DMI linearly (P < 0.01) increased from 10.2 to 10.9 kg/d, whereas, the gain:feed linearly (P < 0.01) decreased from 0.172 to 0.159 without altering the ADG (1.74 kg/d). The wDG was also suggested to be fed as fiber source to replace roughage in finishing diet. Entirely substitution of wDG for roughage of finishing diet decreased (P < 0.01) ruminal pH from 5.95 to 5.75 of beef heifers; however, the ADG and gain:feed of steers were not affected. The results suggested that although substitution of wDG for roughage in finishing diets may increase the incidence of ruminal acidosis, this outcome does not appear to adversely impact the performance of the cattle. The wDG can be successfully incorporated to substitute a portion of grain or roughage within growing and finishing diets with minimal or no adverse impact on cattle growth performance.