Fertilizer or plant growth regulator containing lactic acid bacteria fermentation product
A lactic acid bacteria fermentation composition with mannitol, acetic acid, and monosodium glutamate effectively suppresses bolting in vegetables, enhancing yield by promoting nutrient assimilation and utilization.
Patent Information
- Application Number
- JP2021000315
- Authority / Receiving Office
- JP · JP
- Patent Type
- Patents
- Current Assignee / Owner
- Filing Date
- 2021-01-05
- Publication Date
- 2025-01-10
- Estimated Expiration
- 2041-01-05
AI Technical Summary
Bolting in leafy and root vegetables leads to reduced growth and commercial value due to environmental stresses, and existing methods are inadequate in addressing this issue.
Application of a lactic acid bacteria fermentation composition containing specific ingredients, including mannitol, acetic acid, and monosodium glutamate, to suppress bolting in vegetables.
Reduces bolting rate, allowing for adjusted harvest times and improved yield of leafy and root vegetables by promoting nutrient assimilation and utilization.
Smart Images

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Abstract
Description
[Technical field]
[0001] The present invention relates to an inhibitor for inhibiting bolting in root vegetables and leafy vegetables, utilizing a composition containing a lactic acid bacteria fermentation product, and a method thereof. [Background technology]
[0002] It is known that leafy and root vegetables will develop flower stalks due to changes in temperature and day length, or an extended cultivation period, a phenomenon known as bolting. In leafy and root vegetables, bolting causes the growth of the leaves and roots used as edible parts to stop or become shaped differently than desired, and the taste deteriorates, resulting in a significant decrease or loss of commercial value.
[0003] There are various known causes of flower bolting, but it is known that it occurs more due to environmental stresses such as low light, low temperature, high temperature, lack of fertilizer, lack of water, or excess water rather than optimal environmental factors.
[0004] Known methods for suppressing bolting include applying 5-aminolevulinic acid, its derivatives or its salts (Patent Document 1), adjusting the hours of sunlight using LED lighting or the like (Patent Document 2), using callus induction (Patent Document 3), and using abscisic acid, which is known as a plant hormone (Patent Document 4).
[0005] In addition, various methods for regulating plant growth have been investigated. For example, because phenyllactic acid has a root-promoting effect, methods utilizing lactic acid bacteria have been investigated (Patent Document 5).
[0006] In the food industry, lactic acid bacteria are utilized in a variety of ways, including utilizing the intestinal regulating effects of lactic acid bacteria and using lactic acid bacteria fermentation compositions as seasonings (Patent Documents 6 and 7). [Prior art documents] [Patent documents]
[0007] [Patent Document 1] Patent Publication 2011-121878 [Patent Document 2] Patent Publication No. 2007-252211 [Patent Document 3] JP 6-343360 [Patent Document 4] Patent Publication No. 4-217603 [Patent Document 5] Patent Publication 2014-080398 [Patent Document 6] WO2018 / 110633 [Patent Document 7] Patent Publication No. 2020-103045 Summary of the Invention [Problem to be solved by the invention]
[0008] An objective of the present invention is to provide a method for imparting resistance to plants, such as leafy vegetables and root vegetables, to resistance to biological stress, physical stress, or chemical stress that affects plant growth, in order to improve the yield of the plants. [Means for solving the problem]
[0009] In light of the current situation, the present inventors have conducted intensive research and discovered that application of a lactic acid bacteria fermentation composition containing specific components to root vegetables under normal culture conditions significantly reduces the bolting rate of onions. This led to the completion of the present invention, a composition and method for imparting resistance to plants against biological, physical or chemical stresses that affect growth.
[0010] The present invention is as follows. (1) A plant growth regulator containing a lactic acid bacteria fermentation liquid. (2) A plant growth regulator according to (1), comprising 5 to 70% by mass of mannitol, 1 to 10% by mass of acetic acid, and 1 to 10% by mass of monosodium glutamate. (3) A method for producing the plant growth regulator according to (1) or (2), comprising a step of fermenting a lactic acid bacterium expressing mannitol-2-dehydrogenase in a medium containing a yeast extract containing 5% by mass or more of glutamic acid and fructose. (4) A method for inhibiting bolting in leafy vegetables or root vegetables, which comprises applying the plant growth regulator according to (1) or (2). Effect of the Invention
[0011] According to the present invention, the bolting rate of leafy vegetables or root vegetables can be reduced, and therefore the harvest time of the leafy vegetables or root vegetables can be adjusted, which contributes to improving the rate of high-quality products. Although the mechanism by which the bolting rate is reduced by the present invention has not been elucidated, it is speculated that the application of the lactic acid bacteria fermentation product promotes the assimilation, conversion, and use of nutrients by the plants. [Brief description of the drawings]
[0012] [Figure 1] Results of high quality rate when applied to onions [Diagram 2] Results of bolting rate by application to onion DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0013] The lactic acid bacteria fermentation liquid contained in the plant growth regulator of the present invention is obtained by culturing lactic acid bacteria having mannitol-2-dehydrogenase in a medium containing fructose and yeast extract, and concentrating the culture supernatant. If powdering is required, drying is possible by using an appropriate excipient. The plant growth regulator of the present invention contains 5 to 70% by mass of mannitol, 1 to 10% by mass of acetic acid, and 1 to 10% by mass of sodium glutamate. Lactic acid may be contained in an amount of 1.5 to 20% by mass.
[0014] The mannitol of the present invention is obtained from the fructose used in the medium by the lactic acid bacteria expressing mannitol-2-dehydrogenase in the latter stage. Therefore, the lactic acid bacteria fermentation is performed so that the mannitol content of the present invention becomes the above-mentioned content. The mannitol content can also be adjusted by using an excipient such as dextrin.
[0015] The lactic acid bacteria used in the present invention are not particularly limited as long as they express mannitol-2-dehydrogenase and can be used in food production. For example, lactic acid bacteria expressing mannitol-2-dehydrogenase, such as Lactobacillus or Leuconostoc, can be used.
[0016] Yeast extract is added to the medium used for the lactic acid bacteria fermentation of the present invention. The yeast extract used contains 5% or more glutamic acid. Yeast extract containing 15% or more, and more preferably 20% or more glutamic acid is used. The content of the yeast extract added to the medium may be the same as that of yeast extract normally used in lactic acid bacteria fermentation, and can be adjusted as desired. Such yeast extracts are produced from Torula yeast, brewer's yeast, baker's yeast, and the like. Commercially available yeast extracts may also be used. Commercially available yeast extracts include "Ajitop" from Mitsubishi Corporation Life Sciences, "Hyper Meest" from Asahi Group Foods, and "Himax GL" from Fuji Foods. In the present invention, the glutamic acid content refers to the free glutamic acid in the dry powdered yeast extract, and was measured by an amino acid analyzer L8800 (manufactured by HITACHI) in a conventional manner. By using such yeast extract in the medium, a plant growth regulator containing sodium glutamate can be obtained in the lactic acid fermentation liquor of the present invention. The sodium glutamate content in the lactic acid fermentation liquor of the present invention varies depending on the amount of yeast extract added to the medium, but if the amount added is as in the examples of the present application, the content can be 2 mass% or more.
[0017] In addition to the yeast extract, fructose is used as a medium composition for fermenting the lactic acid bacteria in the previous step. Fructose and glucose can also be used in combination. Liquid sugars containing these can also be used.
[0018] In producing the seasoning of the present invention by fermentation, magnesium chloride, bittern, and other components necessary for lactic acid bacteria fermentation, such as a nitrogen source, a carbon source, vitamins, etc., which are added to a medium during normal lactic acid bacteria fermentation, may be added. The amount of each component added may be appropriately selected from the amounts and types that a person skilled in the art can select for lactic acid bacteria culture.
[0019] The method for producing the plant growth regulator of the present invention will be described below with more specific examples. The above-mentioned medium composition is mixed by a method generally used for lactic acid bacteria fermentation. For example, 100-150 g / L of fructose and 10-50 g / L of yeast extract are mixed and heat sterilized. When minerals necessary for lactic acid bacteria fermentation are added, 0.05-5 ml / L of bittern or the like may be further mixed. After cooling, lactic acid bacteria are cultured. 10-60 g / L of glucose can also be used as a medium component.
[0020] The culture conditions in the present invention can be the temperature and pH generally employed in lactic acid bacteria fermentation. Although the temperature varies depending on the species of bacteria used, the culture is generally performed at 20°C to 40°C, preferably 25°C to 30°C. Furthermore, semi-anaerobic conditions are preferred. During culture, the pH of the culture solution decreases due to the production of organic acids, so the pH during culture may be adjusted with sodium hydroxide, potassium hydroxide, or the like to maintain a pH suitable for the growth of lactic acid bacteria. For example, sodium hydroxide is appropriately added to adjust the medium pH to, for example, pH 5.0 to 6.0.
[0021] The plant growth regulator of the present invention can be obtained by recovering the culture supernatant, which is a lactic acid bacteria fermentation liquid. Specifically, after the end of the culture, the pH of the medium is appropriately adjusted using sodium hydroxide, potassium hydroxide, or the like, if necessary. After the heat treatment, the bacterial cells are removed by centrifugation or filtration, and the culture supernatant is recovered, thereby obtaining the product of the present invention. The recovered culture supernatant may be used as is, or it can be concentrated and dried. There are no particular limitations on the drying method, and known drying methods such as spray drying, drum drying, and freeze drying can be used.
[0022] The lactic acid bacteria fermentation liquid of the present invention produced by the above-mentioned method contains 5 to 70% by mass of mannitol, 1 to 10% by mass of acetic acid, and 1 to 10% by mass of sodium glutamate. The lactic acid content may be 1.5 to 20% by mass. Those skilled in the art of lactic acid bacteria fermentation can appropriately adjust the content of each component within the above range.
[0023] Furthermore, the plant growth regulator of the present invention may be blended with other plant growth regulators, sugars, nitrogen-containing compounds, acids, alcohols, vitamins, trace elements, metal salts, chelating agents, preservatives, antifungal agents, etc., as necessary. These blends can be blended without limitation within a range that does not affect the effects of the present application, and those that can be appropriately selected by a person skilled in the art can be blended. Some examples of other plant growth regulators include indole acetic acid, indole butyric acid, 1-naphthylacetamide agents, 4-CPA agents, gibberellin, cloxifonac, bezylaminopurine, forchlorfenuron, paclobutrazol, uniconazole, inapenfide, chlormequat, calcium carbonate agents, etc. Examples of sugars include glucose, sucrose, galactose, xylose, arabinose, etc., and further, in addition to mannitol produced by lactic acid bacteria fermentation, mannitol may be further added within the range of the content of the present invention. Examples of nitrogen-containing compounds include amino acids and ammonia. Examples of acids include lactic acid, acetic acid, etc., which are produced by lactic acid bacteria fermentation, and may be further added within the range of the content of the present invention, as well as other organic acids, sulfuric acid, phosphoric acid, polyphosphoric acid, etc. Examples of alcohols include methanol, ethanol, etc. Examples of vitamins include vitamin C, vitamin B, nicotinamide, nicotinic acid, folic acid, etc. Examples of metal salts include calcium salts, potassium salts, magnesium salts, etc. Examples of trace elements include boron, manganese, zinc, copper, iron, molybdenum, chlorine, etc.
[0024] The plant growth regulator of the present invention can be used as a fertilizer. The method of application to plants is not particularly limited as long as it is a method that contacts plant bodies such as roots, stems, and leaves, and any application method known in the agricultural and horticultural fields can be adopted. In addition, the method of application to plants can be appropriately determined depending on the type of target plant, etc. For example, application by foliage spray, immersion treatment, soil irrigation, seed treatment, hydroponic solution treatment, fumigation treatment, room temperature fume treatment, etc. can be mentioned as preferred examples. The method of the present invention can be used without being limited by the cultivation form such as soil cultivation or hydroponic cultivation. The application amount can be appropriately determined by those skilled in the art depending on the weather conditions, formulation form, application time, application method, application location, target crop, etc. There is no limit to the number of applications, and it may be applied once or multiple times. When applying multiple times, the methods described in the present specification can be combined. For onions, a method of foliar spraying at the stem and leaf recovery period after the first wintering and at the start of bulb thickening for the second time can be exemplified.
[0025] The cultivation conditions for the plant to which the composition is applied are not particularly limited, and may be cultivation conditions that can be appropriately selected by a person skilled in the art depending on the type of plant to which the composition is applied, the region, the season, and the like.
[0026] The plants to which the present invention is applied are not particularly limited as long as they are leafy vegetables or root vegetables, but examples thereof include onion, garlic, shallot, Chinese chive, leek, chives, shallots, scallions, and other lily family plants, spinach, sugar beet, and other chenopodiaceae, canola, komatsuna, Chinese cabbage, cabbage, radish, turnip, and other Brassicaceae, lettuce, chrysanthemum, burdock, and other Asteraceae, carrot, celery, and other Umbelliferae, ginger, myoga, and other Zingiberaceae, as well as potato, Chinese yam, Chinese yam, taro, lotus root, sweet potato, and bamboo shoot. Furthermore, the varieties of these plants are not particularly limited and can be used. EXAMPLES
[0027] The present invention will now be described in more detail with reference to examples. However, these are merely illustrative and the present invention is not limited to these examples.
[0028] (Example of production of lactic acid bacteria fermentation composition) A medium was prepared by mixing and sterilizing 60g / L glucose, 150g / L fructose, and 50g / L Ajitop (Kohjin Life Sciences). Lactic acid bacteria (Leuconostoc pseudomesenteroides (ATC12291)) were pre-cultured in MRS liquid medium at 37°C for 1 day. 1L of the medium and 10ml of the pre-cultured lactic acid bacteria were placed in a 2L jar fermenter and cultured at 30°C. Aeration was not performed, and the stirring speed was 70 rpm under semi-anaerobic conditions. During the culture, the culture solution was controlled to pH 5.3 with sodium hydroxide, and cultured for 96 hours. After the culture was completed, the pH was adjusted to 6.0 with sodium hydroxide, heated at 90°C for 10 minutes, and then centrifuged at 8,000 rpm for 10 minutes to separate the bacteria and recover the culture supernatant. The collected supernatant was concentrated with an evaporator to obtain a seasoning with a Brix of 70%, which was used as the sample of Example 1. The mannitol content in this sample was 50% by mass. HPLC was used to analyze mannitol, and the measurement conditions were: detector: RI, mobile phase: ultrapure water, column: SUGAR SP0810, column temperature: 80°C, and flow rate: 0.7 ml / min. Dextrin was added to the obtained sample to adjust the mannitol content to 25% by mass, and the sodium glutamate content after the addition of dextrin was 2.7% by mass. In addition, the acetic acid content after the addition of dextrin was 4.0% by mass, and the lactic acid content was 7.0% by mass.
[0029] (Application test to onions) Onions (Neo Earth) were planted in a field and cultivated according to conventional methods. Slow-release fertilizer (sigmoid type) or slow-release fertilizer (linear type) (both from MC Ferticom) was used. The onions were planted three months after sowing, and harvested seven months later for the survey. The product of the present invention was applied in a rice seedling box (size: length 580 x width 280 mm x thickness 28 mm) at 2.0 g per seedling box, twice by foliar spraying after transplanting, the first time at 19 weeks (when stems and leaves recover after wintering) and the second time at 23 weeks (when bulbs start to thicken). For the products other than the present invention, the usual amount of the plant growth agent was applied. Cultivation was carried out on two sides (designated north and south). The results are shown in Figure 1 (excellent product rate) and Figure 2 (stalk bolting rate). 1: control area, 2: liquid fertilizer containing hydrogen peroxide, 3: fertilizer derived from plant extract, 4: seaweed extract fertilizer, and 5: product of the present invention.
[0030] In the test plots to which the product of the present invention was applied, the bolting rate significantly decreased and the rate of excellent products increased.
Claims
1. A plant growth regulator comprising a lactic acid bacteria fermentation liquid containing 5 to 70% by mass of mannitol, 1 to 10% by mass of acetic acid, and 1 to 10% by mass of monosodium glutamate.
2. The method for producing the plant growth regulator according to claim 1, comprising a step of fermenting a lactic acid bacterium expressing mannitol-2-dehydrogenase in a medium containing a yeast extract containing 5 mass% or more of glutamic acid and fructose.
3. A method for inhibiting bolting in leafy vegetables or root vegetables, which comprises applying the plant growth regulator of claim 1.
Citation Information
Patent Citations
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