4.7 Article

Effects on Cell Membrane Integrity of Pichia anomala by the Accumulating Excessive Reactive Oxygen Species under Ethanol Stress

期刊

FOODS
卷 11, 期 22, 页码 -

出版社

MDPI
DOI: 10.3390/foods11223744

关键词

ethanol stress; Pichia anomala; ester production ability; reactive oxygen species; cell membrane integrity

资金

  1. National Natural Science Foundation of China [31960474]
  2. Research Project of State Key Laboratory of Food Science and Technology [SKLFZZB-202116]
  3. Research Project of Brewing Biotechnology and Application Key Laboratory of Sichuan Province [NJ2022-02]

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Ethanol stress inhibits the growth and esters production ability of P. anomala yeast, leading to cell membrane damage and excessive accumulation of ROS. These results are of great significance to the alcohol products brewing industry.
Ethanol stress to yeast is well recognized and exists widely during the brewing process of alcohol products. Pichia anomala is an important ester-producing yeast in the brewing process of Chinese Baijiu and other alcohol products. Therefore, it is of great significance for the alcohol products brewing industry to explore the effects of ethanol stress on the growth metabolism of P. anomala. In this study, the effects of ethanol stress on the growth, esters production ability, cell membrane integrity and reactive oxygen species (ROS) metabolism of P. anomala NCU003 were studied. Our results showed that ethanol stress could inhibit the growth, reduce the ability of non-ethyl ester compounds production and destroy the cell morphology of P. anomala NCU003. The results also showed that 9% ethanol stress produced excessive ROS and then increased the activities of antioxidant enzymes (superoxide dismutase, catalase, aseorbateperoxidase and glutathione reductase) compared to the control group. However, these increased antioxidant enzyme activities could not prevent the damage caused by ROS to P. anomala NCU003. Of note, correlation results indicated that high content of ROS could promote the accumulation of malondialdehyde content, resulting in destruction of the integrity of the cell membrane and leading to the leakage of intracellular nutrients (soluble sugar and protein) and electrolytes. These results indicated that the growth and the non-ethyl ester compounds production ability of P. anomala could be inhibited under ethanol stress by accumulating excessive ROS and the destruction of cell membrane integrity in P. anomala.

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