Scientia Agricultura Sinica ›› 2020, Vol. 53 ›› Issue (5): 1029-1045.doi: 10.3864/j.issn.0578-1752.2020.05.014

• FOOD SCIENCE AND ENGINEERING • Previous Articles     Next Articles

Research Progress of Four Sulfur Compounds Related to Red Wine Flavor

ZHANG QingAn,CHEN BoYu   

  1. School of Food Engineering and Nutrition Sciences, Shaanxi Normal University, Xi’an 710119
  • Received:2019-07-28 Accepted:2019-10-29 Online:2020-03-01 Published:2020-03-14

Abstract:

Sulfur compounds in wines such as glutathione, thiol, hydrogen sulfide and sulfur dioxide are the important flavor compounds, and their content and existing forms greatly affect the wine flavor. The four sulfur compounds are investigated based on the origin and analysis method as well as the winemaking process, while the results on the above aspects are not in agreement in many studies. In this paper, the research progress was summarized about the content, form, origin, analysis method, evolution during storage, and controlling means of the four sulfur compounds in wine. In terms of content and form, the glutathione mainly existed in the reduced form of GSH, and its content was no more than 70 mg?L -1. Thiol might exist in the free form or combined with metal ions, and its content depended on the specific form ranging from ng?L -1 to μg?L -1. Hydrogen sulfide mainly existed in binding state and easily binds to metal ions, and its total content was no more than 30 μg?L -1. Sulfur dioxide often existed in the form of gas or bisulfite (H2SO3 - ) or binds to the carbonyl compounds, and its total content ranged from 64.8 mg?L -1 to 166.5 mg?L -1. In terms of the origin, these four kinds of sulfur compounds were all related to the microorganisms’ metabolic activities during fermentation. To be specific, the glutathione mainly came from the un-fermented grape juice, and a small part came from the amino acid metabolism. Thiol was mainly from the metabolism of the sulfur amino acid and glutathione as well as the chemical synthesis with the hydrogen sulfide as substrate. Hydrogen sulfide mainly came from the sulfur amino acid metabolism, sulfates and sulfites. Sulfur dioxide came from the exogenous additives and the sulfate metabolism. In terms of analysis method, chemical or spectroscopy method was often used, which could be detected quickly to a certain extent, but causing a large error. Regarding the chromatography technique, it had a higher accuracy, but the sample preparation was complicated and the instrument was expensive. The Fenton reaction, i.e. the oxidation initiated by the oxygen and transition metal ions such as iron and copper ion might significantly affect the contents of thiol and hydrogen sulfide during the storage of wine. Finally, to reduce the unpleasant odor caused by some sulfur compounds, some measures could be conducted including optimizing the quality of grape and must, screening the beneficial yeast strains, improving sulfur dioxide addition process and adding metal salts. In conclusion, future researches could be focused on optimizing the detection method, exploring the changing mechanism of the four kinds of sulfur compounds during fermentation and storage, and improving the wine-making process, so as to provide a reference for the winery.

Key words: wine, sulfur compounds, origin, detection method, control means

Fig. 1

Structure of the GSH and GSSG"

Table 1

Comparison of characteristics of four sulfur compounds in wine"

Fig. 2

Main metabolic pathway of four sulfur compounds and relevant enzymes and genes"

Table 2

Comparison between detection methods of sulfur compounds in wine"

含硫化合物
Sulfur compound
前处理方法
Sample preparation
检测方法
Detection method
检测限
Limit of detection
优点或不足
Advantage/drawback
参考文献
Reference
还原型谷胱甘肽
GSH
DNTB处理
Reaction with DTNB
HPLC -DAD 首次完成对葡萄汁中GSH含量检测
Determining GSH content in wine for the first time
[11]
OPA处理
Reaction with OPA
HPLC -FD
0.06 mg∙L-1
排出氧化酶的影响,提高了精确度
Excluding oxidase effect, improving accuracy
[14]
NDA处理
Reaction with NDA
HPLC-FD 0.03 mg∙L-1 提高荧光比率,提高精确度
Improving fluorescence ratio and accuracy
[60]
MBB处理
Reaction with MBB
CE-LIF
0.02 mg∙L-1 样品分离效果好,精确度高
Better sample separation and accuracy
[29]
pBQ处理
Reaction with pBQ
UPLC-ESI-
MS/MS
0.002 mg∙L-1 检测时间短,灵敏度高
Short test time, better sensitivity
[61]
硫醇和硫化氢
Thoil and H2S
p-HMB提取法
Extraction with p-HMB
GC-MS 首次实现这5种硫醇的选择性提取,对3MHA和3MH含量的测定存在误差
Extracting of the 5 compounds selectively for the first time, inaccuracy in quantification of 3MHA and 3MH
[7]
p-HMB提取法
Extraction with p-HMB
GC-MS 0.8 ng∙L-1(4MMP)
15 ng∙L-1(3MH)
5 ng∙L-1(3MHA)
样品分离效果好,精确度高
Better separation and accuracy
[16]
LLE配合Affigel 501
Extraction with LLE coupled with Affigel 501
GC-AED
GC-ITMS-MS
5 ng∙L-1(4MMP)(AED)
15 ng∙L-1(4MMP)(ITMS-MS)
1 ng∙L-1(3MH)(ITMS-MS)
5 ng∙L-1(3MHA)(AED)
0.7 ng∙L-1(3MHA)(ITMS-MS)
首次使用被标记的3MH、3MHA和4MMP作为内标物,克服了被测物被氧化的问题
Using labeled 3MH, 3MHA, 4MMP as internal standard, avoiding sample oxidation
[17]

SPME GC-MS 1.3 ng∙L-1(3MH)
0.25 ng∙L-1(3MHA)
0.03 ng∙L-1(4MMP)
降低基底效应,精确度高
Reducing matrix effect, better accuracy
[18]
HS-SPME GC-pFPD 0.4 μg∙L-1(MeSH)
0.2 μg∙L-1(H2S)
分别检测了游离态和总的MeSH 和H2S含量
Determining both free and total MeSH and H2S content
[19,66]
HP-SPME GC-pFPD 0.8 μg∙L-1(MeSH)
1.3 μg∙L-1(EtSH)
1.7 μg∙L-1(H2S)
受样品氧化及基底效应影响,精确度不高
Causing sample oxidation and matrix effect, not accurate enough
[22]
二氧化硫
SO2
酸性条件蒸馏
Acid conditioned distillation
CFA 5 mg∙L-1(总量 Total) 检测限低,检测速度快,排除了葡萄酒颜色干扰
Lower detection threshold, quick detection, excluding wine color effect
[79]
葡萄酒样品直接与副品红和孔雀绿反应
Reaction with pararosaniline or malachite green
UV-vis 0.6 mg∙L-1(游离态 Free form)
(副品红 Pararosaniline)
0.8 mg∙L-1(总量 Total)
(副品红 Pararosaniline)
0.3 mg∙L-1(游离态 Free form)
(孔雀绿 Malachite green)
0.8 mg∙L-1(总量 Total)
(孔雀绿 Malachite green)
排除了样品处理带来的误差,提高了精确性
Excluding errors caused by sampling, better accuracy
[25]
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