| CPC A01N 63/38 (2020.01) [A01P 3/00 (2021.08); A01P 21/00 (2021.08); C12N 1/14 (2013.01); C12R 2001/885 (2021.05)] | 3 Claims |
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1. A method of growing and inducing resistance of Nicotiana tabacum (N. tabacum), comprising the following specific operation steps:
S1. experimental materials:
S1.1 test media:
a potato dextrose agar (PDA): potato: 200 g, glucose: 20 g, agar: 15 g to 20 g, and distilled water: 1,000 mL; and
an oatmeal agar (OA): oat kernel: 60 g, sucrose: 20 g, agar: 8 g, and distilled water: 1,000 mL; and
S1.2 preparation of bacterial solutions:
inoculating Trichoderma harzianum (T. harzianum) (CGMCC23294) on a PDA plate, cultivating the T. harzianum at 27±1° C. for 5 d to 7 d, and using sterile water to rinse spores from the T. harzianum off to prepare a 1×107 cfu/mL T. harzianum spore suspension for later use; and inoculating Phytophthora nicotianae (P. nicotianae) on an OA plate, cultivating the P. nicotianae at 26±1° C. for 6 d to 7 d, and using sterile water to rinse spores from the P. nicotianae off to prepare a 1×105 cfu/mL P. nicotianae spore suspension for later use;
S2. experimental treatments:
in a greenhouse, collecting a soil in a plough layer of a field as a potting soil, removing weeds and stones from the potting soil, and allowing a resulting soil to pass through a 1×1 cm screen mesh; and adding a compound fertilizer with m(N):m(P2O5):m(K2O)=1:1.5:3 at 1.83 g/kg, mixing, and placing a resulting mixture in pots to obtain a resulting potting soil, wherein each of the pots has an inner opening diameter of 20.5 cm and a height of 13.5 cm, 3 kg of the resulting potting soil is placed per pot;
S2.1 a control treatment:
subjecting first N. tabacum seeds to a surface disinfection to obtain first disinfected N. tabacum seeds, and sowing and cultivating the first disinfected N. tabacum seeds for 50 plants on a first floating seedling tray;
S2.2 a seed soaking treatment:
subjecting second N. tabacum seeds to the surface disinfection to obtain second disinfected N. tabacum seeds, and soaking the second disinfected N. tabacum seeds in the T. harzianum spore suspension for 48 h to obtain soaked seeds; rinsing the soaked seeds with sterile water to obtain rinsed seeds, and sowing the rinsed seeds on a second floating seedling tray to obtain first N. tabacum seedlings; and when the first N. tabacum seedlings reach a seedling establishment stage, transplanting the first N. tabacum seedlings in the pots to obtain first resulting pots, and placing the first resulting pots in the greenhouse;
S2.3 a root irrigation treatment:
disinfecting third N. tabacum seeds to obtain third disinfected N. tabacum seeds, and subjecting the third disinfected N. tabacum seeds to a conventional floating seedling treatment to obtain second N. tabacum seedlings; when the second N. tabacum seedlings reach the seedling establishment stage, transplanting the second N. tabacum seedlings in the pots, with 50 plants in total; and subjecting the second N. tabacum seedlings to the root irrigation treatment with 20 mL of the T. harzianum spore suspension per plant; and
S2.4 a foliar inoculation treatment:
when the second N. tabacum seedlings reach the seedling establishment stage, transplanting the 50 second N. tabacum seedlings, and on a day of the transplanting, evenly spraying 20 mL of the T. harzianum spore suspension on leaves of each of the 50 second N. tabacum seedlings until a leaf surface is covered with a layer of fine water droplets without dripping;
S3. test determination indices and methods:
S3.1 a determination of biological traits:
a determination of growth indices on day 28 after the transplanting: selecting 5 plants from each treatment, determining a plant height, a stem circumference, and a leaf length and a leaf width, and calculating a leaf area of a 5th leaf from a top to a bottom of each plant according to a formula of leaf area=0.6345×leaf length×leaf width, wherein the 5th leaf is the leaf that is counted starting from the top of the plant and proceeding towards the bottom of the plant; pouring the resulting potting soil in the pots out, gently shaking off a soil on a root system, rinsing with clean water, absorbing the water used for rinsing with an absorbent paper, and measuring fresh weights of the aboveground part of the plant and the underground part of the plant; completely scanning the root system by a root scanner for imaging, storing a resulting image in a computer, and using an image analysis system to analyze a total root length, a root surface area, an average root diameter, a root volume, and a branch number; and after the scanning is completed, deactivating the aboveground part and the underground part in a 105° C. oven for 15 min, oven-drying the aboveground part and the underground part at 70° C. to obtain a resulting aboveground part and a resulting underground part, and measuring dry weights of the resulting aboveground part and the resulting underground part and a root-shoot ratio;
S3.2 a determination of physiological and biochemical indexes:
on day 7, day 14, day 21, and day 28 after the transplanting, collecting 0.5 g of a fourth leaf from the top to the bottom in each treatment with a leaf vein avoided, wherein the fourth leaf is the leaf that is counted starting from the top of the plant and proceeding towards the bottom of the plant, and determining a chlorophyll content by an acetone-ethanol extraction colorimetric method; measuring an activity of the root system by a triphenyltetrazolium chloride (TTC) method; and determining an activity of a root nitrate reductase (NR) by in vivo spectrophotometry, wherein 3 replicates are set for each treatment; and
S3.3 a determination of disease resistance and induced resistance indexes:
on day 28 after the transplanting in each treatment, evenly inoculating 20 mL of the 1×105 cfu/mL P. nicotianae spore suspension into the soil around the root system of each plant through the root irrigation treatment, and 14 days later, investigating an incidence of each treatment and calculating a disease index and a control effect of each treatment; and
collecting a root sample from an N. tabacum plant in each treatment, and determining activities of a peroxidase (POD), a polyphenol oxidase (PPO), a phenylalanine ammonia lyase (PAL), and a catalase (CAT), wherein 3 replicates are set for each treatment; and
S4. data processing:
subjecting data to a difference significance test.
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