食品科学 ›› 2022, Vol. 43 ›› Issue (21): 305-314.doi: 10.7506/spkx1002-6630-20210910-129

• 包装贮运 • 上一篇    

包装方式和贮藏温度对羊肉微生物数量、细菌多样性和代谢途径的影响

王莹,张建海,王勇亮,来静,张鑫,周丽媛,朱迎春   

  1. (1.山西农业大学食品科学与工程学院,山西 太谷 030801;2.山西农业大学动物医学学院,山西 太谷 030801;3.山西省食品研究所,山西 太原 030000)
  • 发布日期:2022-12-12
  • 基金资助:
    山西省重点研发计划项目(201903D211008);山西省自然科学基金面上项目(20210302123400); 山西省农谷建设科研专项(SXNGJSKYZX201903)

Effect of Packaging Method and Storage Temperature on Bacterial Load, Diversity and Metabolic Pathways in Mutton

WANG Ying, ZHANG Jianhai, WANG Yongliang, LAI Jing, ZHANG Xin, ZHOU Liyuan, ZHU Yingchun   

  1. (1. College of Food Science and Engineering, Shanxi Agricultural University, Taigu 030801, China;2. College of Animal Medicine, Shanxi Agricultural University, Taigu 030801, China; 3. Shanxi Food Research Institute, Taiyuan 030000, China)
  • Published:2022-12-12

摘要: 为探究包装方式和贮藏温度对羊肉微生物数量、细菌多样性和代谢途径的影响,将宰后羊肉分别经空气包装(air packaging,AP)、真空包装(vacuum packaging,VP)和贴体包装(skin packaging,SP)后置于冷藏(4±1)℃和冰温(-1.7±0.2)℃下贮藏30 d,采用平板计数和高通量测序相结合的方法对贮藏过程中的微生物群落进行分析。结果表明,贮藏过程中SP组的菌落总数(total viable count,TVC)、乳酸菌、假单胞菌等6 种菌群数量均低于AP组和VP组,冰温组6 种菌群数量均明显低于冷藏组。随贮藏时间延长羊肉菌群多样性均呈下降趋势,冷藏组较冰温组多样性更复杂。采用高通量测序技术对羊肉菌群16S rDNA的V3~V4区域测序,共获得10 个菌门和30 个菌属,所有样品中丰度最高的菌门均为变形菌门(Proteobacteria)和厚壁菌门(Firmicutes);假单胞菌属(Pseudomonas)在AP组中为优势菌属,而在SP组和VP组中丰度较低,肉食杆菌属(Carnobacterium)、环丝菌属(Brochothrix)和乳杆菌属(Lactobacillus)均为AP、VP和SP组贮藏末期的优势菌属。基于京都基因与基因组百科全书富集分析发现碳水化合物代谢、氨基酸代谢和核苷酸代谢为羊肉贮藏过程中主要代谢途径,其中贮藏前期以氨基酸代谢为主,贮藏后期主要为碳水化合物代谢和核苷酸代谢,包装方式和贮藏温度导致的菌群结构差异主导了代谢丰度的不同。结论:SP协同冰温贮藏能够降低羊肉贮藏过程中微生物的数量和细菌群落多样性,有利于保持羊肉品质。

关键词: 贮藏温度;包装方式;微生物数量;细菌多样性;代谢途径

Abstract: To investigate the effects of packaging method and storage temperature on the bacterial load, diversity and metabolic pathways in mutton, postportem mutton was stored in air packaging (AP), vacuum packaging (VP) or skin packaging (SP) for 30 days at chilled ((4 ± 1) ℃) or superchilled temperature ((?1.7 ± 0.2) ℃). The bacterial community composition during the storage period was analyzed by a combination of plate counting and high-throughput sequencing. The results showed that total viable count (TVC), Lactobacillus count, Pseudomonas count, Staphylococcus/Micrococcus count, mold and yeast count, and psychrophilic bacterial count were all lower in the SP group than in the AP and VP groups, and all the bacterial counts were significantly lower in the superchilled storage group than in the chilled storage group. The bacterial diversity showed a decreasing trend with storage time, and it was more complex in the chilled storage group than in the superchilled storage group. A total of 30 bacterial genera belonging to 10 bacterial phyla were obtained by high-throughput sequencing of the V3–V4 region of the 16S rDNA gene. For all samples, the most abundant phyla were Proteobacteria and Firmicutes. Pseudomonas was the dominant genus in the AP group but less abundant in the SP and VP groups. Carnobacterium, Brochothrix and Lactobacillus were the dominant genera at the end of storage for all three groups. The Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis revealed that carbohydrate, amino acid and nucleotide metabolism were the major metabolic pathways during the storage of mutton. Amino acid metabolism was dominant during the early storage period, while carbohydrate and nucleotide metabolism were dominant during the late storage period. The difference in metabolic abundance was mainly attributed to the difference in microflora structure caused by packaging methods and storage temperatures. In conclusion, SP combined with superchilled temperature can reduce the microbial load and community diversity in mutton during storage, helping to maintain the quality of mutton.

Key words: storage temperature; packaging method; microbial load; bacterial diversity; metabolic pathways

中图分类号: