CN115669717B - Compound preservation method for Lanzhou lily bulbs - Google Patents
Compound preservation method for Lanzhou lily bulbs Download PDFInfo
- Publication number
- CN115669717B CN115669717B CN202211370586.1A CN202211370586A CN115669717B CN 115669717 B CN115669717 B CN 115669717B CN 202211370586 A CN202211370586 A CN 202211370586A CN 115669717 B CN115669717 B CN 115669717B
- Authority
- CN
- China
- Prior art keywords
- lily
- bulbs
- lily bulbs
- bulb
- cys
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 241000234435 Lilium Species 0.000 title claims abstract description 154
- 238000000034 method Methods 0.000 title claims abstract description 40
- 238000004321 preservation Methods 0.000 title claims abstract description 24
- 150000001875 compounds Chemical class 0.000 title claims abstract description 22
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims abstract description 107
- 238000011282 treatment Methods 0.000 claims abstract description 79
- 239000004201 L-cysteine Substances 0.000 claims abstract description 29
- 235000013878 L-cysteine Nutrition 0.000 claims abstract description 29
- 230000002335 preservative effect Effects 0.000 claims abstract description 11
- 239000003755 preservative agent Substances 0.000 claims abstract description 10
- 238000005057 refrigeration Methods 0.000 claims abstract description 8
- 238000002791 soaking Methods 0.000 claims abstract description 5
- 238000011010 flushing procedure Methods 0.000 claims abstract description 4
- 230000035699 permeability Effects 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000002131 composite material Substances 0.000 claims description 6
- 230000005855 radiation Effects 0.000 claims description 3
- 241000233855 Orchidaceae Species 0.000 claims 3
- 238000003860 storage Methods 0.000 abstract description 75
- 235000016709 nutrition Nutrition 0.000 abstract description 6
- 230000035764 nutrition Effects 0.000 abstract description 5
- 230000036541 health Effects 0.000 abstract description 3
- 241000894006 Bacteria Species 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 abstract description 2
- 238000005260 corrosion Methods 0.000 abstract description 2
- 230000000694 effects Effects 0.000 description 50
- 230000004580 weight loss Effects 0.000 description 24
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 18
- 229920002472 Starch Polymers 0.000 description 13
- 235000019698 starch Nutrition 0.000 description 13
- 239000008107 starch Substances 0.000 description 13
- 102000019197 Superoxide Dismutase Human genes 0.000 description 12
- 108010012715 Superoxide dismutase Proteins 0.000 description 12
- 102000016938 Catalase Human genes 0.000 description 11
- 108010053835 Catalase Proteins 0.000 description 11
- WSMYVTOQOOLQHP-UHFFFAOYSA-N Malondialdehyde Chemical compound O=CCC=O WSMYVTOQOOLQHP-UHFFFAOYSA-N 0.000 description 11
- 229940118019 malondialdehyde Drugs 0.000 description 11
- 102000003820 Lipoxygenases Human genes 0.000 description 10
- 108090000128 Lipoxygenases Proteins 0.000 description 10
- 230000003078 antioxidant effect Effects 0.000 description 10
- 230000003111 delayed effect Effects 0.000 description 10
- 239000003963 antioxidant agent Substances 0.000 description 9
- 235000010323 ascorbic acid Nutrition 0.000 description 9
- 229960005070 ascorbic acid Drugs 0.000 description 9
- 239000011668 ascorbic acid Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 235000000346 sugar Nutrition 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- 235000013399 edible fruits Nutrition 0.000 description 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 7
- 230000008859 change Effects 0.000 description 7
- 238000006731 degradation reaction Methods 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 description 6
- MBDOYVRWFFCFHM-UHFFFAOYSA-N 2-hexenal Chemical compound CCCC=CC=O MBDOYVRWFFCFHM-UHFFFAOYSA-N 0.000 description 6
- 102000004190 Enzymes Human genes 0.000 description 6
- 108090000790 Enzymes Proteins 0.000 description 6
- 230000032683 aging Effects 0.000 description 6
- 235000006708 antioxidants Nutrition 0.000 description 6
- 210000000170 cell membrane Anatomy 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 239000012528 membrane Substances 0.000 description 6
- 210000003470 mitochondria Anatomy 0.000 description 6
- 239000003642 reactive oxygen metabolite Substances 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 239000000796 flavoring agent Substances 0.000 description 5
- 235000019634 flavors Nutrition 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- HRHOWZHRCRZVCU-AATRIKPKSA-N (E)-hex-2-enyl acetate Chemical compound CCC\C=C\COC(C)=O HRHOWZHRCRZVCU-AATRIKPKSA-N 0.000 description 4
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 4
- OHDRQQURAXLVGJ-HLVWOLMTSA-N azane;(2e)-3-ethyl-2-[(e)-(3-ethyl-6-sulfo-1,3-benzothiazol-2-ylidene)hydrazinylidene]-1,3-benzothiazole-6-sulfonic acid Chemical compound [NH4+].[NH4+].S/1C2=CC(S([O-])(=O)=O)=CC=C2N(CC)C\1=N/N=C1/SC2=CC(S([O-])(=O)=O)=CC=C2N1CC OHDRQQURAXLVGJ-HLVWOLMTSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000013068 control sample Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 235000012055 fruits and vegetables Nutrition 0.000 description 4
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 4
- -1 isopentyl aldehyde Chemical class 0.000 description 4
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 4
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 230000009758 senescence Effects 0.000 description 4
- 150000008163 sugars Chemical class 0.000 description 4
- MBDOYVRWFFCFHM-SNAWJCMRSA-N 2-Hexenal Natural products CCC\C=C\C=O MBDOYVRWFFCFHM-SNAWJCMRSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000009825 accumulation Methods 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 230000002255 enzymatic effect Effects 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 230000003859 lipid peroxidation Effects 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000002035 prolonged effect Effects 0.000 description 3
- 230000029058 respiratory gaseous exchange Effects 0.000 description 3
- DTCCTIQRPGSLPT-ONEGZZNKSA-N (E)-2-pentenal Chemical compound CC\C=C\C=O DTCCTIQRPGSLPT-ONEGZZNKSA-N 0.000 description 2
- NDFKTBCGKNOHPJ-AATRIKPKSA-N (E)-hept-2-enal Chemical compound CCCC\C=C\C=O NDFKTBCGKNOHPJ-AATRIKPKSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 description 2
- ICMAFTSLXCXHRK-UHFFFAOYSA-N Ethyl pentanoate Chemical compound CCCCC(=O)OCC ICMAFTSLXCXHRK-UHFFFAOYSA-N 0.000 description 2
- 241001634096 Lilium martagon Species 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000004075 alteration Effects 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- DTCCTIQRPGSLPT-UHFFFAOYSA-N beta-Aethyl-acrolein Natural products CCC=CC=O DTCCTIQRPGSLPT-UHFFFAOYSA-N 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 230000002438 mitochondrial effect Effects 0.000 description 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
- 238000005502 peroxidation Methods 0.000 description 2
- 235000013824 polyphenols Nutrition 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 230000002000 scavenging effect Effects 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 235000019587 texture Nutrition 0.000 description 2
- HRHOWZHRCRZVCU-UHFFFAOYSA-N trans-hex-2-enyl acetate Natural products CCCC=CCOC(C)=O HRHOWZHRCRZVCU-UHFFFAOYSA-N 0.000 description 2
- 230000005068 transpiration Effects 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- LVBXEMGDVWVTGY-VOTSOKGWSA-N (E)-oct-2-enal Chemical compound CCCCC\C=C\C=O LVBXEMGDVWVTGY-VOTSOKGWSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N 4-Methyl-3-penten-2-one, 9CI Chemical compound CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 241001258887 Lilium davidii var. unicolor Species 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 241000669298 Pseudaulacaspis pentagona Species 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-M Superoxide Chemical compound [O-][O] OUUQCZGPVNCOIJ-UHFFFAOYSA-M 0.000 description 1
- 208000031971 Yin Deficiency Diseases 0.000 description 1
- 230000036579 abiotic stress Effects 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- 150000003797 alkaloid derivatives Chemical class 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000006851 antioxidant defense Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000019522 cellular metabolic process Effects 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000004665 defense response Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000006353 environmental stress Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000004345 fruit ripening Effects 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- NDFKTBCGKNOHPJ-UHFFFAOYSA-N hex-2-enal Natural products CCCCC=CC=O NDFKTBCGKNOHPJ-UHFFFAOYSA-N 0.000 description 1
- AILKHAQXUAOOFU-UHFFFAOYSA-N hexanenitrile Chemical compound CCCCCC#N AILKHAQXUAOOFU-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 230000035800 maturation Effects 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000004065 mitochondrial dysfunction Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 150000005856 steroid saponins Chemical class 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- LVBXEMGDVWVTGY-UHFFFAOYSA-N trans-2-octenal Natural products CCCCCC=CC=O LVBXEMGDVWVTGY-UHFFFAOYSA-N 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention discloses a compound preservation method of Lanzhou lily bulbs, which comprises the following steps: (1) Selecting, stripping and flushing fresh picked lily bulbs; (2) carrying out UV-C irradiation treatment within 24 hours after lily bulb picking; (3) And (3) soaking the whole treated lily bulb in L-cysteine solution, naturally airing, storing in a preservative film, and placing in a refrigeration house. The method disclosed by the invention can achieve the purposes of resisting bacteria and corrosion, ensures the safety of the lily bulbs, accords with the pursuit of modern people on nature, safety, green, nutrition and health, can also prolong the storage period of the lily bulbs, and is suitable for popularization and application.
Description
Technical Field
The invention relates to a preservation method of lily bulbs, in particular to a compound preservation method of Lanzhou lily bulbs.
Background
Lily (Lilium davidii var. Unicolor) is a variety of Sichuan lily, a natural plant widely planted in Lanzhou, gansu province, china. The lily bulb has rich meat quality, white scales are held and overlapped, is rich in various nutritional ingredients and active substances such as carbohydrate, protein, vitamins, minerals, polyphenol, steroid saponin, alkaloid and the like, has unique aromatic flavor, and is a medicine and food dual-purpose plant for the first pass of the ministry of health in China. According to the records of the pharmacopoeia of the people's republic of China, the lily has the effects of nourishing yin, moistening lung, clearing heart fire and soothing nerves, can be used for treating cough due to yin deficiency, insomnia and dreaminess, and in recent years, domestic and foreign researches prove that the lily has anti-tumor, anti-inflammatory and anti-oxidation activities. However, because lily bulbs have high water content, high respiration rate, poor photosensitivity and the like, phenomena such as water loss, purple, brown stain, mildew, decay and the like are easy to occur, and the industrial development of fresh lily in Lanzhou is hindered.
The preservation technology of lily bulbs is realized mainly by controlling the following four aspects: (1) Reducing the respiration intensity of lily bulbs, reducing nutrition loss and delaying post maturation aging; (2) The transpiration is reduced, and the higher water content of lily bulbs is maintained; (3) preventing microbial infection and inhibiting microbial growth; (4) Avoiding mechanical damage and environmental stress, and membrane lipid peroxidation. At present, the traditional fresh-keeping technology of lily bulbs comprises common refrigeration fresh-keeping, air-conditioned storage fresh-keeping and sulfur fumigation technology fresh-keeping, but the fresh-keeping method has the defects of common fresh-keeping effect, high fresh-keeping cost and potential safety hazard. Aiming at the problems of deterioration of quality, microbial growth, short shelf life and the like of lily products in Lanzhou, the research on a novel fresh-keeping technology is very necessary, and the method is green, convenient and low in cost.
Disclosure of Invention
The invention aims to solve the technical problem of providing a compound preservation method for Lanzhou lily bulbs, and relates to a green compound preservation method for whole bulb UV-C irradiation treatment, bulb chemical preservative (L-cysteine) soaking treatment and refrigeration.
The invention relates to a compound fresh-keeping method for Lanzhou lily bulbs, which comprises the following steps:
(1) Selecting, stripping and flushing fresh picked lily bulbs;
(2) Carrying out UV-C irradiation treatment within 24 hours after lily bulb picking;
(3) And (3) soaking the whole treated lily bulb in L-cysteine solution, naturally airing, storing in a preservative film, and placing in a refrigeration house.
The invention relates to a compound preservation method of Lanzhou lily bulbs, which comprises the following steps before the step (1): the stripped lily scales are treated by adopting weight loss rate, color difference screening UV-C dosage and L-cysteine concentration, wherein the UV-C dosage is 3.0kJ/m 2、3.5kJ/m2、4.0kJ/m2、4.5kJ/m2 and 5.0kJ/m 2 respectively, the L-cysteine solution concentration is 0.5g/L, 1.0g/L, 1.5g/L, 2.0g/L and 2.5g/L respectively, the screened UV-C irradiation dosage is 4.5kJ/m -2, and the L-cysteine solution concentration is 2.0g/L.
The invention relates to a compound preservation method for Lanzhou lily bulbs, which comprises the following specific steps: to hang the UV-C lamp tube with an emission wavelength of 254nm horizontally on the radiation container.
The invention relates to a compound preservation method for Lanzhou lily bulbs, wherein the irradiation dose of UV-C is 4.5kJ/m -2.
The invention relates to a compound preservation method for Lanzhou lily bulbs, wherein the distance between a UV-C lamp tube and a tray is 15cm, the lily bulbs are placed on the tray, and the lily bulbs are slightly and horizontally rotated for 180 degrees in the middle of irradiation time.
The invention relates to a compound preservation method for lily bulbs, wherein the concentration of L-cysteine solution in the step (3) is 2.0g/L, and the lily bulbs are soaked for 15min.
The invention relates to a compound preservation method for Lanzhou lily bulbs, wherein the preservative film has good air permeability and water permeability.
The invention relates to a compound fresh-keeping method for Lanzhou lily bulbs, wherein the temperature of a refrigeration house is 2+/-0.5 ℃ and the humidity is 90%.
The compound application of UV-C irradiation and L-cysteine in lily bulb preservation.
The compound fresh-keeping method of the Lanzhou lily bulbs is different from the prior art in that: the compound preservation method of the Lanzhou lily bulbs provided by the invention has the advantages that the UV-C irradiation dose and the L-cysteine concentration of the after-harvest treatment of the Lanzhou lily bulbs are clear, the low-temperature refrigeration is combined, and then the storage period is effectively prolonged through the quality change after the harvest, the removal of active oxygen and the activity of self-defense enzymes, so that a novel preservation method is provided for the preservation of the Lanzhou lily bulbs.
The picked lily bulbs are subjected to 4.5kJ/m -2 UV-C irradiation treatment, and the decay of the lily bulbs can be effectively inhibited by combining 2.0g/L L-cysteine treatment with cold storage preservation, so that the color, appearance and smell of the lily bulbs are kept, the loss of nutrient components is prevented, the aging process is delayed, and the storage period can reach 50 days. After the preparation, UV-C irradiation is combined with L-cysteine treatment, the fresh-keeping modes are different, and the irradiation dose and the L-cysteine concentration obtained by the method are obtained by analyzing the quality, nutrition, flavor, aging and other indexes on the basis of multiple experiments, and the method has reliability and operability.
The invention has the beneficial effects that:
(1) The lily bulbs are subjected to UV-C irradiation treatment, so that the color difference change and weight loss of the lily bulbs are inhibited, and the fresh-keeping effect of the lily bulbs can be effectively improved.
(2) The lily bulbs subjected to UV-C irradiation treatment are soaked in L-cysteine solution, so that the decay phenomenon of the lily bulbs is inhibited, the quality of the lily bulbs is maintained, and the storage period is prolonged.
The lily bulb preservation method disclosed by the invention can achieve the purposes of resisting bacteria and preventing corrosion, ensures the safety of lily bulbs, accords with the pursuit of modern people on nature, safety, green, nutrition and health, can also prolong the storage period of the lily bulbs, and is suitable for popularization and application.
The method for preserving the Lanzhou lily bulbs in a composite manner is further described below with reference to the accompanying drawings.
Drawings
FIG. 1 is the effect of different doses of UV-C treatment on lily bulb weight loss rate;
FIG. 2 is a graph showing the effect of different concentrations of L-cysteine on lily bulb weight loss rate;
FIG. 3 is the effect of different doses of UV-C treatment on color differences during cold storage of lilium;
FIG. 4 is a graph showing the effect of different concentrations of L-cysteine on color differences during cold storage of lily of Lanzhou;
FIG. 5 is the effect of different treatments on the appearance of lily bulbs;
FIG. 6 is the effect of different treatments on the rotting rate of lily bulbs;
FIG. 7 is the effect of different treatments on lily bulb weight loss rate;
FIG. 8 is the effect of different treatments on lily bulb hardness;
FIG. 9 is the effect of different treatments on lily bulb chromatic aberration;
FIG. 10 is the effect of different treatments on lily bulb starch;
FIG. 11 is the effect of different treatments on lily bulb reducing sugars;
FIG. 12 is the effect of different treatments on lily bulb total phenols;
FIG. 13 is the effect of different treatments on lily bulb ascorbic acid;
FIG. 14 is the effect of different treatments on lily bulb volatile components; wherein, the numbers 1-36 respectively represent the following substances: ethyl acetate-M, trans-2-hexenyl acetate, ethyl acetate-D, 2-heptanone, isoamyl alcohol-D, ethyl valerate, nonanal, n-octanal, heptanal, dipentene, 4-isopropyltoluene, capronitrile, trans-2-nonanal, isopentyl aldehyde, isobutyraldehyde, trans-2-pentenal, 1-penten-3-one, tetrahydrofuran-D, tetrahydrofuran-M, styrene, 3-hydroxy-2-butanone, 2, 3-butanediol, isoamyl alcohol-M, ethyl butyrate, 1-penten-3-one, isopropyl acetate, 2-hexenal, n-hexanal-M, n-hexanal-D, isopropylidene acetone, (E) -2-heptenal, trans-2-octenal, 2-hexenal, methyl acetate and 2-n-amyl furan;
FIG. 15 is the effect of different treatments on lily bulb hydrogen peroxide;
FIG. 16 is the effect of different treatments on lily bulb superoxide anions;
FIG. 17 is the effect of different treatments on lily bulb lipoxygenase;
FIG. 18 is the effect of different treatments on lily bulb malondialdehyde;
FIG. 19 is the effect of different treatments on lily bulb superoxide dismutase;
FIG. 20 is the effect of different treatments on lily bulb catalase;
FIG. 21 is the effect of different treatments on the oxidation resistance of lily bulbs;
FIG. 22 is the effect of different treatments on lily bulb ultrastructure;
All english chinese translations that appear in the figures are as follows:
DECAY RATE: decay rate;
Time: time;
Weight loss: weight loss;
Firmness: hardness;
Starch: starch;
Reducing sugamer: reducing sugar;
Total phenolic content: total phenol content;
Ascorbic acid: ascorbic acid;
h 2O2 content:H2O2 content;
o 2 production rate:O2 ·- content;
LOX activity: LOX activity;
MDA content: MDA content;
SOD activity: SOD activity;
CAT ACTIVITY: CAT activity;
ABTS SCAVENGING CAPACITY: ABTS purge capability.
Detailed Description
Example 1
A fresh-keeping method of lily bulbs comprises the following steps:
(1) Selecting, stripping and flushing fresh picked lily bulbs; it is to be reminded that the freshly harvested lily bulbs are pretreated by the horses, so that the freshness of the lily bulbs is maintained.
(2) The UV-C irradiation treatment is carried out within 24h after picking the bulb of lily, wherein the treatment method is to horizontally hang a UV-C lamp tube with the emission wavelength of 254nm (TUV, 30W, philips) on a radiation container, the distance from the tray is 15cm, place the bulb of lily on the tray, and slightly horizontally rotate the bulb of lily by 180 degrees in the middle of irradiation time so as to ensure uniform irradiation. UV-C optimum irradiation dose: 4.5kJ/m -2.
(3) Immersing the whole lily bulb after treatment in L-cysteine solution for 15min, wherein the optimal concentration of the L-cysteine is as follows: 2.0g/L. Naturally airing, storing in a preservative film with good air permeability and water permeability, and placing in a refrigeration house with the temperature of 2+/-0.5 ℃ and the humidity of 90 percent to obtain the UV-C/L-cys group lily bulbs.
Preferably, before step (1), the method further comprises the following steps:
screening UV-C dosage and L-cysteine concentration by adopting weight loss rate and chromatic aberration to treat the stripped lily scales;
UV-C dose: 3.0, 3.5, 4.0, 4.5, 5.0kJ/m 2;
L-cysteine: 0.5, 1.0, 1.5, 2.0, 2.5g/L;
As can be seen from FIG. 1, the weight loss rate of lily increases gradually with the storage time. The weight loss rate of the ultraviolet treated lily was lower than that of the control sample throughout the storage period. On day 15 of storage, the weight loss rates of the control and UV dose treated samples were 9.43.+ -. 0.28% and 4.48.+ -. 0.13% respectively at 4.5kJ/m 2. The uv dose was 5.0kJ/m 2 with the lowest weight loss rate, significantly different (P < 0.05) compared to the weight loss rate of the control sample, but not significantly different (P > 0.05) from the 4.0kJ/m 2,4.5kJ/m2,5.0kJ/m2 treated group.
As can be seen from FIG. 2, the weight loss rate of lily increases gradually with the storage time. The weight loss of L-cysteine treated lily was lower than that of the control samples throughout the storage period. On day 15 of storage, the weight loss rates of the control and L-cysteine treated samples at concentrations of 2.0g/L were 12.14.+ -. 0.35% and 6.31.+ -. 0.62%, respectively. The L-cysteine treatment group concentration was the lowest at 2.0g/L weight loss rate, with a significant difference (P < 0.05) compared to the weight loss rate of the other treated samples.
As can be seen from fig. 3, during storage, the Δe value of lilium martagon increased with increasing storage time, and the Δe value of the control sample was always higher than that of the UV-C treated sample. This is probably due to the fact that the ultraviolet treatment inhibits the activity of the enzyme activity related to the color change, thereby inhibiting the enzymatic browning and delaying the browning of the lily scales. The delta E value of 4.5kJ/m 2 was 6.29.+ -. 0.88% for the UV treatment at day 15 of storage, significantly lower than for the other treated samples (P < 0.05). Therefore, the ultraviolet light of 4.5kJ/m 2 can well reduce the color change of the lily.
As can be seen from fig. 4, during storage, the Δe value of lilium martagon increased with increasing storage time, and the Δe value of the control sample was always higher than that of the L-cysteine treated sample. This is probably due to the fact that the L-cysteine treatment inhibits the activity of the enzyme activity related to the color change, thereby inhibiting the enzymatic browning and delaying the browning of the lily scales. On day 15 of storage, L-cysteine treated 2.0g/L had a ΔE value of 5.63.+ -. 0.39% which was significantly lower than that of the other treated samples (P < 0.05). Therefore, the L-cysteine treatment of 2.0g/L can well reduce the change of the color of the lily.
Comparative example 1
A fresh-keeping method of lily bulbs comprises the following steps:
Naturally airing the whole cleaned and finished lily bulbs, carrying out uniform UV-C irradiation treatment, and placing the whole cleaned and finished lily bulbs into a refrigerator with the temperature of 2+/-0.5 ℃ and the humidity of 90% at the irradiation dose of 4.5kJ/m -2 to obtain the UV-C group lily bulbs.
Comparative example 2
A fresh-keeping method of lily bulbs comprises the following steps:
Soaking the whole cleaned and finished lily bulbs in L-cysteine solution for 15min, naturally airing, storing in a preservative film with good air permeability and water permeability, and placing in a refrigerator with the temperature of 2+/-0.5 ℃ and the humidity of 90% to obtain L-cys group lily bulbs.
Comparative example 3
A fresh-keeping method of lily bulbs comprises the following steps:
And naturally airing the cleaned and finished whole lily bulbs, storing the whole lily bulbs in a preservative film with good air permeability and water permeability, and putting the preservative film in a cold storage with the temperature of 2+/-0.5 ℃ and the humidity of 90% to obtain the CK-group lily bulbs.
The lily bulbs treated in example 1 and comparative examples 1 to 3 were observed, analyzed and detected, and are specifically shown in fig. 1 to 18.
1. Comparison of Lily bulb appearance during storage
The surface color of a fruit or vegetable is one of the criteria reflecting consumer purchase decisions. As shown in fig. 5, the control bulbs became purple and began to brown when stored for 10 days, while the UV-C/L-cys treated bulbs remained white at 30 days and slightly purple when stored for 40 days, indicating that UV-C/L-cys treatment delayed the degradation of the lily bulb appearance by about 30 days.
2. Comparison of Lily bulb rot Rate during storage
The decay rate is a main parameter for evaluating the quality of the picked lily bulbs. The decay rate of all groups increased with increasing storage time. As shown in FIG. 6, decay of the UV-C treated group was delayed by 10 days, and decay of the L-cys treated group and UV-C/L-cys treated group were delayed by 20 days, as compared to the control group. At the end of the storage time (50 days), the decay rates of the UV-C, L-cys-treated and UV-C/L-cys-treated groups were 60.00.+ -. 5.00%, 50.00.+ -. 0.00% and 33.33.+ -. 2.89%, respectively, the control group was 81.67.+ -. 2.89%, with a significant difference (P < 0.05).
3. Comparison of the weight loss ratio of Lily bulb during storage
Weight loss is one of important indexes for evaluating edible quality of lily bulbs. In general, weight loss of fruits and vegetables can affect their appearance, texture, flavor and nutrition and accelerate their deterioration during storage. As shown in fig. 7, the weight loss of both control and treatment lily bulbs continuously increased during storage, which is mainly related to higher transpiration and respiration rates. There was a significant difference between the control and treatment groups (P < 0.05) over the first 10 days of storage, whereas there was no significant difference between single and composite fresh keeping (P > 0.05). After 15 days of storage, the UV-C/L-cys treated group had the lowest weight loss (5.80.+ -. 0.37%), followed by the L-cys treated group (6.45.+ -. 0.08%), the UV-C treated group (7.01.+ -. 0.26%) and the control group (8.98.+ -. 0.52%). These results indicate that UV-C/L-cys treatment is a potential method of preserving lily bulb weight during storage.
4. Comparison of Lily bulb hardness during storage
Hardness is a key parameter that reflects the ripeness and softness of fruit and also affects consumer acceptance of fruit. Figure 8 reflects the effect of different treatments on the hardness during storage of lily bulbs. The hardness of the control group decreased with increasing storage time, reaching a minimum of 55.72.+ -. 0.58N at 50 days. The hardness of the UV-C and L-cys groups was higher than that of the control group at the same time, but significantly (P < 0.05) lower than that of the UV-C/L-cys treated group (66.94.+ -. 2.03N), consistent with the weight loss results.
5. Comparison of lily bulb color differences during storage
Fig. 9 shows that the Δe values of the control bulbs increased sharply during storage and then reached a peak at 40 days. All treatment groups remained at a lower level during 50 days of storage with no significant increase and no significant difference (P > 0.05) between single and composite fresh keeping. The results also show that the bulbs of the control group begin to become purple and brown after 10 days of storage, and the single fresh-keeping treatment and the compound fresh-keeping treatment can effectively delay the trend.
6. Comparison of Lily bulb starch content during storage
Lily bulbs are a kind of fruit rich in starch, which is the main energy storage substance for carbohydrates in vegetables and fruits. As shown in fig. 10, the starch content of the bulbs continuously decreases during storage, which can be explained by the fact that starch is easily hydrolyzed in the presence of amylase and converted to soluble sugars, resulting in bulbs that taste sweeter and softer in texture during aging. The control group was reduced from 78.12.+ -. 0.24g/kg to 41.72.+ -. 1.02g/kg when stored for 50 days. However, the UV-C treatment, L-cys treatment and UV-C/L-cys treatment groups were 48.52.+ -. 0.82g/kg, 49.41.+ -. 0.47g/kg and 56.87.+ -. 1.91g/kg, respectively, significantly delayed starch degradation. These results indicate that UV-C/L-cys treatment is more advantageous in delaying the conversion of starch to sugar than UV-C treatment and L-cys treatment, thereby slowing down the senescence and softening of lily bulbs.
7. Comparison of the content of lily bulb reducing sugar during storage
Reducing sugars play an important role in plant architecture and metabolism at the cellular and whole organism level and can also be involved in plant defense responses under adverse environmental conditions. In the control and treatment groups, the reducing sugar content was reduced and then increased throughout the storage period (fig. 11). This decrease may be due to the continuous consumption of reducing sugars during the initial stages of storage to maintain normal physiological activity of the plant, while the increase during the later stages of storage may be related to starch degradation. The results also show that control and UV-C treated bulbs start to increase at 20 days of storage, and that L-cys and UV-C/L-cys treatments can effectively retard this trend, which starts to increase at 30 days of storage. The CK group was elevated and reached a peak of 1.15.+ -. 0.04g/kg on day 50. All treatments delayed their accumulation and the UV-C/L-cys treatment group performed best in maintaining a relatively stable level of reducing sugar water, consistent with the variation in starch content.
8. Comparison of the Total phenol content of Lily bulb during storage
Phenolic compounds are considered as members of the non-enzymatic antioxidant system, which can effectively scavenge reactive oxygen species and prevent oxidative damage. As shown in fig. 12, the total phenol content in the control and treated fruits tended to rise from 0-30 days, which can be explained by the accelerated senescence of lily bulbs with prolonged storage time, resulting in an increase in total phenol content. After 30 days of storage, the CK group declined sharply, with the lowest decline rate in the UV-C/L-cys treated group, which may be related to oxidation of phenols to quinones later in storage. These results indicate that UV-C/L-cys treatment can increase the total phenol content of lily bulbs to combat postharvest senescence.
9. Comparison of the content of Lily bulb ascorbic acid during storage
The content of the ascorbic acid can be used as an important index for resisting aging of fruits and evaluating the quality of the fruits. Figure 13 reflects the effect of different treatments on the ascorbic acid content of lily bulbs. It can be seen that the ascorbic acid content of the different treatments tended to decrease, whereas the ascorbic acid content of the UV-C/L-cys treated group was significantly higher than that of the other groups after 50 days of storage (P < 0.05). These results indicate that the UV-C/L-cys treatment is effective in delaying the decrease of the ascorbic acid content in the lily bulbs, thereby maintaining the oxidation resistance of the lily bulbs during storage.
10. Comparison of the content of volatile components of Lily bulb during storage
The changes in volatile components of lily bulbs in different treatment groups of 0 day, 30 day, and 50 day were analyzed by HS-GC-IMS method, and as shown in FIG. 14, after 50 days of storage, the contents of ethyl acetate, trans-2-hexenyl acetate, ethyl valerate, 2-hexenal, nonanal, octanal, isopentanol, and 2-heptanone were higher than those in the groups of CK, UV-C, and L-cys. Most of these compounds are typical fruity volatile compounds, and the odor is pleasant, which may be responsible for the fresh bulb flavor, suggesting that UV-C/L-cys treatment may protect the aromatic volatile compounds or may facilitate their release. During storage, the CK group produces some irritating substances with bad flavors, such as isopentyl aldehyde, isobutyraldehyde, trans-2-pentenal, 1-penten-3-one, and tetrahydrofuran. In contrast, UV-C/L-cys treatment inhibited the production of these substances.
11. Comparison of the Hydrogen peroxide (H 2O2) content of Lily bulb during storage
The close relationship between fruit senescence and active oxygen (e.g., H 2O2 and O 2 ·-) is considered a by-product of normal cellular metabolism. As shown in fig. 15, the H 2O2 content of all groups of lily bulbs gradually increased throughout the storage period. The control group increased sharply during its storage period, especially from 40 days to 50 days, however, the UV-C, L-cys and UV-C/L-Cy treated groups significantly delayed this trend of increase (P < 0.05).
12. Comparison of the content of superoxide anions (O 2 ·-) in Lily bulb during storage
O 2 ·- is an important index for detecting active oxygen. As shown in fig. 16, the O 2 ·- production rate of the control lily bulb gradually increased with the increase of the storage time. Despite the large fluctuations of the UV-C and L-cys treated groups, the overall trend was still rising and O 2 ·- was significantly suppressed. When the UV-C/L-cys treated group was stored for 50 days, the O 2 ·- production rate was 5.62.+ -. 0.28mmol/min/kg, which was reduced by 44% compared to the control group. These results indicate that UV-C/L-cys treatment can delay senescence and degradation of lily bulbs by reducing the O 2 ·- production rate, i.e., accumulation of active oxygen.
13. Comparison of Lily bulb Lipoxygenase (LOX) Activity during storage
Reactive Oxygen Species (ROS) increase the permeability of cell membranes and the hydrolysis of cell membrane phospholipids, leading to peroxidation and degradation of cell membranes. Lipoxygenase (LOX) catalyzes membrane lipids, the major component of cell membranes, and produces small hydrocarbon fragments. As shown in fig. 17, LOX activity was gradually increased in the control group and the treatment group. The control group had higher LOX activity, which is consistent with high H 2O2 content and O 2 ·- production rate. In contrast, UV-C, L-cys and UV-C/L-cys treatments delayed the upward trend of LOX activity (P < 0.05), indicating that UV-C/L-cys treatment can delay membrane lipid peroxidation.
14. Comparison of the content of Malondialdehyde (MDA) in Lily bulb during storage
Malondialdehyde (MDA) is the end product of membrane lipid peroxidation and is considered an indicator of the severity of cell membrane damage. As shown in fig. 18, the MDA contents of the control group and the treatment group gradually increased. The control group had a higher MDA content, which is consistent with a high H 2O2 content and O 2 ·- production rate. In contrast, UV-C, L-cys and UV-C/L-cys treatment delayed the rising trend of MDA content (P < 0.05), indicating that UV-C/L-cys treatment can delay malondialdehyde accumulation and delay aging.
15. Comparison of Lily bulb superoxide dismutase (SOD) Activity during storage
When fruits and vegetables are subjected to abiotic stress, the dynamic balance of intracellular ROS production and clearance is disrupted, resulting in damage to proteins, nucleic acids, and cellular structures. Antioxidant enzymes are critical to the protection of fruits and vegetables from temperature stress by maintaining an antioxidant system. Superoxide dismutase (SOD) is a typical antioxidant enzyme. SOD can remove superoxide radical in biological cells to generate hydrogen peroxide and oxygen. FIG. 19 shows that the SOD activity of lily bulbs increases slightly from 0 days to 20 days, rises rapidly within the following 10 days, and decreases rapidly from 30 days to the end of storage. UV-C, L-cys and UV-C/L-cys treatment significantly increased the SOD activity during storage (P < 0.05).
16. Comparison of Lily bulb Catalase (CAT) Activity during storage
Catalase (CAT) is a typical antioxidant enzyme. CAT can catalyze the formation of oxygen and water from hydrogen peroxide catalyzed by SOD, and as shown in FIG. 20, CAT activity of all groups increased slightly from 0 days to 20 days and decreased rapidly from 20 days to the end of storage. UV-C, L-cys and UV-C/L-cys treatment significantly increased CAT activity during storage (P < 0.05).
17. Comparison of the antioxidant Properties of Lily bulb during storage
ABTS scavenging ability is one of the accepted methods for evaluating the total antioxidant capacity of fruits and vegetables. As shown in FIG. 21, all groups increased and decreased, UV-C, L-cys and UV-C/L-cys treatments significantly enhanced the ability of the ABTS to clear during storage (P < 0.05). This suggests that the treatment group not only activates the antioxidant defense system of the bulbs, which may be partially reflected in increasing SOD and CAT activity, but also may directly increase antioxidant capacity. Furthermore, some previous studies found that there is a good correlation between antioxidant capacity and total phenol, so the enhanced antioxidant capacity of UV-C/L-cys treatment may also be attributed to maintaining a higher total phenol content.
18. Comparison of ultrastructural control of lily bulbs during storage
In addition to peroxidation and degradation of cell membranes, mitochondria are particularly vulnerable to active oxygen. In general, excess reactive oxygen species can lead to mitochondrial dysfunction. To demonstrate the preservative effect of UV-C/L-cys, the ultrastructural structure of mitochondria was observed with a transmission electron microscope at the end of storage of lily bulbs. For the CK group (fig. 22A), the mitochondria were relatively few, the matrix density was low, the membrane structure was discontinuous, damaged in some places, and the intracellular compartments were destroyed. Most mitochondria swell and partially disintegrate, resulting in leakage of matrix. In addition, since the phenolic compound is oxidized to quinone, the black particles aggregate, and thus many black particles are formed. Less swollen and damaged mitochondria and black particles appear in the UV-C treated bulbs (fig. 22B). FIG. 18CD shows that L-cys-treated and UV-C/L-cys-treated bulbs contain a number of mitochondria. Most mitochondrial cristae were tightly aligned, the double membrane structure was clear, and there was no apparent swelling, consistent with the treatment of reducing H 2O2 content and O 2 ·- production rate. Notably, UV-C/L-cys treated bulbs contained spherical starch particles, which were associated with slow degradation of starch in the treated group. These results indicate that at the end of storage, control bulbs delayed this change in the UV-C/L-cys treated group due to ROS attack, mitochondrial rupture, metabolic disturbance.
The above examples are only illustrative of the preferred embodiments of the present invention and are not intended to limit the scope of the present invention, and various modifications and improvements made by those skilled in the art to the technical solution of the present invention should fall within the scope of protection defined by the claims of the present invention without departing from the spirit of the present invention.
Claims (4)
1. A compound preservation method of Lanzhou lily bulbs is characterized by comprising the following steps: the method comprises the following steps:
(1) Selecting, stripping and flushing fresh picked lily bulbs;
(2) Carrying out UV-C irradiation treatment within 24 hours after lily bulb picking;
(3) Soaking the whole lily bulb in L-cysteine solution, naturally airing, storing in a preservative film, and placing in a refrigeration house;
wherein the irradiation dose of the UV-C is 4.5 kJ/m 2, the concentration of the L-cysteine solution is 2.0g/L, the temperature of the refrigerator is 2+/-0.5 ℃ and the humidity of the refrigerator is 90 percent.
2. The method for composite preservation of lily bulbs in orchid according to claim 1, which is characterized in that: the UV-C irradiation treatment in the step (2) adopts the following method: a UV-C lamp tube with an emission wavelength of 254nm was suspended horizontally on the radiation container.
3. The method for composite preservation of lily bulbs in orchid according to claim 2, which is characterized in that: the UV-C lamp tube is 15cm away from the tray, the lily bulb is placed on the tray, and the lily bulb is gently and horizontally rotated for 180 degrees in the middle of the irradiation time.
4. The method for composite preservation of lily bulbs in orchid according to claim 1, which is characterized in that: the preservative film has good air permeability and water permeability.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211370586.1A CN115669717B (en) | 2022-11-03 | 2022-11-03 | Compound preservation method for Lanzhou lily bulbs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202211370586.1A CN115669717B (en) | 2022-11-03 | 2022-11-03 | Compound preservation method for Lanzhou lily bulbs |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115669717A CN115669717A (en) | 2023-02-03 |
CN115669717B true CN115669717B (en) | 2024-05-03 |
Family
ID=85047693
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202211370586.1A Active CN115669717B (en) | 2022-11-03 | 2022-11-03 | Compound preservation method for Lanzhou lily bulbs |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN115669717B (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102986861A (en) * | 2012-12-27 | 2013-03-27 | 甘肃农业大学 | Lanzhou dried lily bulb sulfur-free color fixative and using method thereof |
CN105475462A (en) * | 2015-11-27 | 2016-04-13 | 西北师范大学 | Method for cleaning, color protection and fresh keeping of fresh edible Lanzhou lily |
CN106615084A (en) * | 2016-12-15 | 2017-05-10 | 南宁学院 | Preservation method of fresh-cut Chinese yam |
CN107801770A (en) * | 2017-10-19 | 2018-03-16 | 双流县公兴三跨蔬菜农场 | A kind of method of fresh-keeping of vegetables |
CN115152837A (en) * | 2022-07-11 | 2022-10-11 | 西南科技大学 | Method for inhibiting browning of fresh-cut mushrooms |
-
2022
- 2022-11-03 CN CN202211370586.1A patent/CN115669717B/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102986861A (en) * | 2012-12-27 | 2013-03-27 | 甘肃农业大学 | Lanzhou dried lily bulb sulfur-free color fixative and using method thereof |
CN105475462A (en) * | 2015-11-27 | 2016-04-13 | 西北师范大学 | Method for cleaning, color protection and fresh keeping of fresh edible Lanzhou lily |
CN106615084A (en) * | 2016-12-15 | 2017-05-10 | 南宁学院 | Preservation method of fresh-cut Chinese yam |
CN107801770A (en) * | 2017-10-19 | 2018-03-16 | 双流县公兴三跨蔬菜农场 | A kind of method of fresh-keeping of vegetables |
CN115152837A (en) * | 2022-07-11 | 2022-10-11 | 西南科技大学 | Method for inhibiting browning of fresh-cut mushrooms |
Also Published As
Publication number | Publication date |
---|---|
CN115669717A (en) | 2023-02-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Mahunu et al. | Improving the biocontrol efficacy of Pichia caribbica with phytic acid against postharvest blue mold and natural decay in apples | |
Mirdehghan et al. | Effects of salicylic acid, jasmonic acid, and calcium chloride on reducing chilling injury of pomegranate (Punica granatum L.) fruit | |
Awad | Effect of post-harvest salicylic acid treatments on fruit quality of peach cv." Flordaprince" during cold storage. | |
Zhou et al. | The biocontrol of postharvest decay of table grape by the application of kombucha during cold storage | |
Liu et al. | Effect of ozone treatment on the quality and enzyme activity of Lentinus edodes during cold storage | |
Ravi et al. | Review on tropical root and tuber crops. II. Physiological disorders in freshly stored roots and tubers | |
Zhang et al. | Effect of lemon essential oil-enriched coating on the postharvest storage quality of citrus fruits | |
Chen et al. | The preharvest and postharvest application of salicylic acid and its derivatives on storage of fruit and vegetables: A review | |
Xie et al. | Melatonin treatment improves postharvest quality and regulates reactive oxygen species metabolism in “Feizixiao” litchi based on principal component analysis | |
CN113854352A (en) | Method for prolonging preservation period of square bamboo fresh bamboo shoots | |
CN112514984A (en) | Stress fresh-keeping method and flexible package suitable for storing and transporting thin-skin grapes | |
CN114600954B (en) | Leaf vegetable fresh-keeping method combining carrageenan oligosaccharide coating with LED composite illumination and air conditioning | |
Nazoori et al. | Carboxymethyl cellulose and carnauba wax treatments kept the pomegranate fruit (Punica granatum L.) quality during cold storage via improving enzymatic defense system and bioactive compounds | |
Hazarika et al. | Alteration of quality attributes and shelf-life in strawberry (Fragaria× ananassa) fruits during storage as influenced by edible coatings | |
Shakerardekani et al. | Enhancing the quality of fresh pistachio fruit using sodium alginate enriched with thyme essential oil | |
Steffens et al. | Quality of “Cripps Pink” apples following the application of 1‐MCP, ethanol vapor and nitric oxide as pretreatments for controlled atmosphere storage | |
Guo et al. | Effect of high O2 treatments on physiochemical, lycopene and microstructural characteristics of cherry tomatoes during storage | |
CN115152832A (en) | Essential oil microcapsule, preparation method thereof and grape storage method | |
Öz et al. | Postharvest hexanal application delays senescence and maintains quality in persimmon fruit during low‐temperature storage | |
CN115669717B (en) | Compound preservation method for Lanzhou lily bulbs | |
Devi et al. | Effect of calcium and salicylic acid on quality retention in relation to antioxidative enzymes in radish stored under refrigerated conditions | |
CN113349247B (en) | Pretreatment process for refrigerating and refreshing square bamboo fresh bamboo shoots | |
Shao et al. | Outcomes of 1‐MCP combined with aerosolization of ε‐polylysine antimicrobials on storage quality of flat peach | |
CN115812902A (en) | Method for improving quality of fresh waxy corn by inhibiting respiration and oxygen permeation | |
Lee et al. | Effects of pre-drying, delayed cooling, and carbon dioxide on skin blackening disorder in Asian pear (Pyrus pyrifolia Nakai)‘Chuhwangbae’ |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |