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从奶牛瘤胃中分离出尿素分解菌Z129并进行泛基因组分析。

Isolation and pan-genome analysis of Z129, a ureolytic bacterium, from the rumen of dairy cow.

作者信息

Zhong Huiyue, Zheng Nan, Wang Jiaqi, Zhao Shengguo

机构信息

State Key Laboratory of Animal Nutrition, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, China.

出版信息

Front Microbiol. 2023 Apr 6;14:1169973. doi: 10.3389/fmicb.2023.1169973. eCollection 2023.

Abstract

INTRODUCTION

Urea is an important non-protein nitrogen source for ruminants. In the rumen, ureolytic bacteria play critical roles in urea-nitrogen metabolism, however, a few ureolytic strains have been isolated and genomically sequenced. The purpose of this study was to isolate a novel ureolytic bacterial strain from cattle rumen and characterize its genome and function.

METHODS

The ureolytic bacterium was isolated using an anaerobic medium with urea and phenol red as a screening indicator from the rumen fluid of dairy cattle. The genome of isolates was sequenced, assembled, annotated, and comparatively analyzed. The pan-genome analysis was performed using IPGA and the biochemical activity was also analyzed by test kits.

RESULTS

A gram-positive ureolytic strain was isolated. Its genome had a length of 4.52 Mbp and predicted genes of 4223. The 16S rRNA gene and genome GTDB-Tk taxonomic annotation showed that it was a novel strain of , and it was named Z129. The pan-genome analysis showed that Z129 had the highest identity to ATCC 49162 with a genome average nucleotide identity of 98.69% and possessed 238 unique genes. Strain Z129 was the first strain isolated from the rumen as we know. The functional annotation of the Z129 genome showed genes related to urea metabolism, including urea transport (AE), nickel ion transport (J, B, A, B, D, and A), urease activation (A-ureG) and ammonia assimilation (A, A, B, E, L, A, B, and D) were present. Genes involved in carbohydrate metabolism were also present, including starch hydrolysis (E), cellulose hydrolysis (B and X), xylose transport (FH) and glycolysis (, , A, , A, , , L). Biochemical activity analysis showed that Z129 was positive for alkaline phosphatase, leucine arylamidase, acid phosphatase, naphthol-AS-BI-phosphohydrolase, α-glucosidase, β-glucosidase, and pyrrolidone arylaminase, and had the ability to use D-ribose, L-arabinose, and D-lactose. Urea-nitrogen hydrolysis rate of Z129 reached 55.37% at 48 h of incubation.

DISCUSSION

Therefore, the isolated novel ureolytic strain Z129 had diverse nitrogen and carbon metabolisms, and is a preferred model to study the urea hydrolysis mechanism in the rumen.

摘要

引言

尿素是反刍动物重要的非蛋白氮源。在瘤胃中,尿素分解菌在尿素氮代谢中起关键作用,然而,仅有少数尿素分解菌株被分离并进行了基因组测序。本研究的目的是从牛瘤胃中分离出一种新型尿素分解细菌菌株,并对其基因组和功能进行表征。

方法

以含有尿素和酚红作为筛选指标的厌氧培养基从奶牛瘤胃液中分离尿素分解菌。对分离菌株的基因组进行测序、组装、注释和比较分析。使用IPGA进行泛基因组分析,并通过试剂盒分析其生化活性。

结果

分离出一株革兰氏阳性尿素分解菌株。其基因组长度为4.52 Mbp,预测基因有4223个。16S rRNA基因和基因组GTDB-Tk分类注释表明它是一种新型菌株,命名为Z129。泛基因组分析表明,Z129与ATCC 49162的同一性最高,基因组平均核苷酸同一性为98.69%,拥有238个独特基因。据我们所知,Z129菌株是从瘤胃中分离出的首例该种菌株。Z129基因组的功能注释显示存在与尿素代谢相关的基因,包括尿素转运(AE)、镍离子转运(J、B、A、B、D和A)、脲酶激活(A-ureG)和氨同化(A、A、B、E、L、A、B和D)。也存在参与碳水化合物代谢的基因,包括淀粉水解(E)、纤维素水解(B和X)、木糖转运(FH)和糖酵解(、、A、、A、、、L)。生化活性分析表明,Z129对碱性磷酸酶、亮氨酸芳基酰胺酶、酸性磷酸酶、萘酚-AS-BI-磷酸水解酶、α-葡萄糖苷酶、β-葡萄糖苷酶和吡咯烷芳基酰胺酶呈阳性反应,并且具有利用D-核糖、L-阿拉伯糖和D-乳糖的能力。在培养48小时时Z129的尿素氮水解率达到55.37%。

讨论

因此,分离出的新型尿素分解菌株Z129具有多样的氮和碳代谢,是研究瘤胃中尿素水解机制的优选模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a2a/10117971/5b0c79ba415c/fmicb-14-1169973-g001.jpg

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