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从瘤胃液中分离和鉴定酵母以用作反刍动物饲料添加剂的潜力研究

Isolation and Characterization of Yeasts from Rumen Fluids for Potential Use as Additives in Ruminant Feeding.

作者信息

Suntara Chanon, Cherdthong Anusorn, Wanapat Metha, Uriyapongson Suthipong, Leelavatcharamas Vichai, Sawaengkaew Jutaporn, Chanjula Pin, Foiklang Suban

机构信息

Tropical Feed Resources Research and Development Center (TROFREC), Department of Animal Science, Faculty of Agriculture, Khon Kaen University, Khon Kaen 40002, Thailand.

Fermentation Research Center for Value Added Agricultural Products (FerVAAP), Department of Biotechnology, Faculty of Technology, Khon Kaen University, Khon Kaen 40002, Thailand.

出版信息

Vet Sci. 2021 Mar 19;8(3):52. doi: 10.3390/vetsci8030052.

DOI:10.3390/vetsci8030052
PMID:33808746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8003577/
Abstract

is a yeast strain often used to improve the feed quality of ruminants. However, has limited capacity to provide biomass when inoculated with carbon sources and a low ability to produce cellulase enzymes. Here, we hypothesized that yeast in the rumen produces a large amount of biomass and could release cellulase enzymes to break down fiber content. Therefore, the aim of this study was to screen, isolate and identify yeast from the rumen fluids of Holstein Friesian steers and measure the efficiency of biomass production and cellulase activity. A fermentation medium containing sugarcane molasses as a carbon source and urea as a nitrogen source was optimized. Two fistulated-crossbred Holstein Friesian steers averaging 350 ± 20 kg body weight were used to screen and isolate the ruminal yeast. Two experiments were designed: First, a 12 × 3 × 3 factorial was used in a completely randomized design to determine biomass and carboxymethyl cellulase activity. Factor A was the isolated yeast and . Factor B was sugarcane molasses (M) concentration. Factor C was urea (U) concentration. In the second experiment, potential yeasts were selected, identified, and analyzed for 7 × 4 factorial use in a completely randomized design. Factor A was the incubation times. Factor B was the isolated yeast strains, including codes H-Khon Kaen University (KKU) 20 (as -KKU20), I-KKU20 (-KKU20), and C-KKU20 (as sp.-KKU20). Isolation was imposed under aerobic conditions, resulting in a total of 11 different colonies. Two appearances of colonies including asymmetric colonies of isolated yeast (indicated as A, B, C, E, and J) and ovoid colonies (coded as D, F, G, H, I, and K) were noted. Isolated yeast from the rumen capable of providing a high amount of biomass when inoculant consisted of the molasses 15% + urea 3% (M15 + U3), molasses 25% + urea 1% (M25 + U1), molasses 25% + urea 3% (M25 + U3), and molasses 25% + urea 5% (M25 + U5) when compared to the other media solution ( < 0.01). In addition, 11 isolated biomass-producing yeasts were found in the media solution of M25 + U1. There were 4 isolates cellulase producing yeasts discovered in the media solution of M25 + U1 and M25 + U5 whereas molasses 5% + urea 1% (M5 + U1), molasses 5% + urea 3% (M5 + U3), molasses 5% + urea 5% (M5 + U5), molasses 15% + urea 1% (M15 + U1), molasses 15% + urea 3% (M5 + U3), and M25 + U3 were found with 2, 3, 1, 2, 1, and 2 isolates, respectively. Ruminal yeast strains H-KKU20, I-KKU20, and C-KKU20 were selected for their ability to produce biomass. Identification of isolates H-KKU20 and I-KKU20 revealed that those isolates belonged to -KKU20 and -KKU20 while C-KKU20 was identified as sp.-KKU20. Two strains provided maximum cell growth: -KKU20 (9.78 and 10.02 Log cell/mL) and -KKU20 (9.53 and 9.6 Log cells/mL) at 60 and 72 h of incubation time, respectively. The highest ethanol production was observed in at 76.4, 77.8, 78.5, and 78.6 g/L at 36, 48, 60, and 72 h of incubation time, respectively ( < 0.01). The -KKU20 yielded the least reducing sugar at about 30.6 and 29.8 g/L at 60 and 72 h of incubation time, respectively. The screening and isolation of yeasts from rumen fluids resulted in 11 different yeasts being obtained. The potential yeasts discovered in the rumen fluid of cattle were -KKU20, -KKU20, and sp.-KKU20. -KKU20 had higher results than the other yeasts in terms of biomass production, cellulase enzyme activity, and cell number.

摘要

是一种常用于提高反刍动物饲料质量的酵母菌株。然而,在接种碳源时其提供生物量的能力有限,且产生纤维素酶的能力较低。在此,我们假设瘤胃中的酵母能产生大量生物量,并能释放纤维素酶以分解纤维成分。因此,本研究的目的是从荷斯坦弗里生公牛的瘤胃液中筛选、分离和鉴定酵母,并测定生物量生产效率和纤维素酶活性。优化了一种以甘蔗 molasses 作为碳源和尿素作为氮源的发酵培养基。使用两头平均体重为 350 ± 20 kg 的带瘘管杂交荷斯坦弗里生公牛来筛选和分离瘤胃酵母。设计了两个实验:首先,采用 12×3×3 析因设计,以完全随机设计来确定生物量和羧甲基纤维素酶活性。因素 A 是分离出的酵母和……。因素 B 是甘蔗 molasses(M)浓度。因素 C 是尿素(U)浓度。在第二个实验中,选择潜在酵母进行鉴定,并采用 7×4 析因设计在完全随机设计中进行分析。因素 A 是培养时间。因素 B 是分离出的酵母菌株,包括编号为 H - 孔敬大学(KKU)20(记为 -KKU20)、I - KKU20(-KKU20)和 C - KKU20(记为 sp.-KKU20)。在有氧条件下进行分离,共得到 11 个不同的菌落。注意到两种菌落形态,包括分离出的酵母的不对称菌落(标记为 A、B、C、E 和 J)和卵形菌落(编码为 D、F、G、H、I 和 K)。当接种物由 15%molasses + 3%尿素(M15 + U3)、25%molasses + 1%尿素(M25 + U1)、25%molasses + 3%尿素(M25 + U3)和 25%molasses + 5%尿素(M25 + U5)组成时,与其他培养基溶液相比,从瘤胃中分离出的酵母能够提供大量生物量(P < 0.01)。此外,在 M25 + U1 的培养基溶液中发现了 11 种分离出的产生物量酵母。在 M25 + U1 和 M25 + U5 的培养基溶液中发现了 4 种产纤维素酶酵母,而在 5%molasses + 1%尿素(M5 + U1)、5%molasses + 3%尿素(M5 + U3)、5%molasses + 5%尿素(M5 + U5)、15%molasses + 1%尿素(M15 + U1)、15%molasses + 3%尿素(M5 + U3)和 M25 + U3 中分别发现了 2、3、1、2、1 和 2 种分离物。瘤胃酵母菌株 H-KKU20、I-KKU20 和 C-KKU20 因其产生生物量的能力而被选中。对分离物 H-KKU20 和 I-KKU20 的鉴定表明,这些分离物属于 -KKU20 和 -KKU20,而 C-KKU20 被鉴定为 sp.-KKU20。两种菌株在培养 60 和 72 h 时分别提供了最大细胞生长:-KKU20(9.78 和 10.02 Log 细胞/mL)和 -KKU20(9.53 和 9.6 Log 细胞/mL)。在培养 36、48、60 和 72 h 时,分别观察到最高乙醇产量为 76.4、77.8、78.5 和 78.6 g/L(P < 0.01)。-KKU20 在培养 60 和 72 h 时分别产生约 30.6 和 29.8 g/L 的还原糖,产量最低。从瘤胃液中筛选和分离酵母得到了 11 种不同的酵母。在牛的瘤胃液中发现的潜在酵母是 -KKU20、-KKU20 和 sp.-KKU20。-KKU20 在生物量生产、纤维素酶活性和细胞数量方面的结果高于其他酵母。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/8003577/48a4bd6ec07d/vetsci-08-00052-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/8003577/ef246907b7bd/vetsci-08-00052-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/8003577/48a4bd6ec07d/vetsci-08-00052-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/8003577/ef246907b7bd/vetsci-08-00052-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/8003577/bf11087d0258/vetsci-08-00052-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/8003577/48a4bd6ec07d/vetsci-08-00052-g005.jpg

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