KR20080101148A - The manufaturing process of plant growth promoter composition using fermetation productions of effective microorganisms - Google Patents

The manufaturing process of plant growth promoter composition using fermetation productions of effective microorganisms Download PDF

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KR20080101148A
KR20080101148A KR1020070047496A KR20070047496A KR20080101148A KR 20080101148 A KR20080101148 A KR 20080101148A KR 1020070047496 A KR1020070047496 A KR 1020070047496A KR 20070047496 A KR20070047496 A KR 20070047496A KR 20080101148 A KR20080101148 A KR 20080101148A
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plant growth
composition
plant
fermentation product
bacteria
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차준철
김용환
송정우
김은경
조재영
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
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    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/225Lactobacillus
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    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/38Pseudomonas

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Abstract

A method of manufacturing a composition for promoting growth of plant is provided to increase a chlorophyll in a plant body using nature fermentation product of useful microorganism such as lactobacillus, photosynthetic bacteria, yeast and Bacillus, to make color of stem and leaf deep, to accelerate growth of the leaf and root, to promote coloring of fruit and to prevent failure of the growth of plant. A method of manufacturing a composition for promoting growth of plant comprises steps of: obtaining many fermentation products 1 containing a material promoting growth of plant by cultivating independently photosynthetic bacteria which is a useful microorganism in a fermentation medium; obtaining a fermentation product 2 in which many bioactive substances, enzymes, antioxidants, organic acids are contained by forming a symbiotic relation by mixing and inoculating various useful microorganism such as lactobacillus, photosynthetic bacteria, yeast and Bacillus to the other fermentation medium; and mixing the fermentation product 1 and the fermentation product 2 at a regular rate.

Description

유용미생물의 천연 발효산물을 이용한 식물 생장촉진용 조성물의 제조방법{The manufaturing process of plant growth promoter composition using fermetation productions of effective microorganisms}The manufaturing process of plant growth promoter composition using fermetation productions of effective microorganisms}

도 1은 본 발명의 식물 생장촉진용 조성물 처리에 따른 열무의 엽록소 함량을 비교한 그래프이다. 1 is a graph comparing the chlorophyll content of radish according to the treatment method for plant growth promoting composition of the present invention.

도 2는 본 발명의 식물 생장촉진용 조성물 내에 함유되어 있는 각종 유기산을 HPLC로 분석한 그래프이다.Figure 2 is a graph analyzing the various organic acids contained in the plant growth promoting composition of the present invention by HPLC.

도 3은 본 발명의 식물 생장촉진용 조성물 처리에 따른 열무의 생육정도를 비교한 사진도이다.Figure 3 is a photograph showing a comparison of the growth of radish according to the treatment method for plant growth promotion of the present invention.

본 발명은 식물 생장촉진용 조성물의 제조방법에 관한 것으로서, 보다 구체 적으로는 일정한 조성의 발효배지에 유용미생물인 광합성세균을 단독 배양하여 식물 생장촉진 물질을 다량 함유한 발효산물 1을 얻고 또 다른 발효배지에 유산균, 광합성세균, 효모, 바실러스 등 다양한 유용미생물을 혼합 접종하여 공생관계를 형성케 함으로써 천연의 생리활성물질, 효소, 항산화물질, 유기산이 다량 함유된 발효산물 2를 얻어 각각 일정한 비율로 혼합함으로써 식물 생장촉진용 조성물을 제조하는 방법에 관한 것이다. The present invention relates to a method for preparing a composition for promoting plant growth, and more specifically, to obtain a fermentation product 1 containing a large amount of plant growth promoting material by culturing photosynthetic bacteria, which is useful for fermentation medium of a certain composition, alone. By inoculating mixed fermentation medium with various useful microorganisms such as lactic acid bacteria, photosynthetic bacteria, yeast, and Bacillus to form a symbiotic relationship, obtain fermentation products 2 containing a large amount of natural physiologically active substances, enzymes, antioxidants, and organic acids. It relates to a method for producing a composition for promoting plant growth by mixing.

종래에 상용화되고 있는 식물 생장촉진제는 식물호르몬을 화학적 합성과 같은 일련의 제조 과정을 거쳐 제품화한 경우와 식물호르몬을 분비하는 특성을 가진 특정 미생물을 직접 제품화하는 경우가 있다. 식물호르몬은 영양소가 아닌 유기물질로써 특정농도에서 특정한 생리, 생화학적 또는 형태학적 반응을 일으키는 물질로써 현재 식물생장촉진물질로 상업적으로 이용되는 물질은 지베렐린(gibberellin), 오옥신(auxin), 사이토키닌(cytokinin), ABA, 에틸렌 등 다양한 물질들이 있으며, 국내에는 상기 물질을 포함한 25종의 물질이 식물생장조절제로 고시되어 있다. 그러나 식물호르몬은 다양한 작물이 아닌 특정 작물에만 작용되는 단점이 있을 수 있으며, 처리농도, 적용시기, 적용방법 등을 달리하였을 경우 작물의 이상 비대화 등의 원인이 되어 품질 및 높은 수확량을 기대하기가 어려운 경우가 있다. 또한 식물호르몬의 대부분이 수입품으로서 고가일 뿐만 아니라 용액 제조 시 지베렐린 이외에는 물에 잘 용해되지 않아 용해제로서 알콜을 사용해야함으로 알콜이 식물체 내로 침투하여 열을 발생시켜 식물을 시들게 하는 등 여러가지 문제점을 가지고 있다. Plant growth promoters that are conventionally commercialized may be produced when a plant hormone is produced through a series of manufacturing processes, such as chemical synthesis, and directly commercialized a specific microorganism having a characteristic of secreting plant hormones. Phytohormones are organic substances that are not nutrients and cause specific physiological, biochemical or morphological reactions at specific concentrations. Currently, commercially available plant growth promoters are gibberellin, auxin and cytokinin. There are various substances such as (cytokinin), ABA, and ethylene, and 25 kinds of substances including the above are reported in the plant growth regulators in Korea. However, phytohormones may have disadvantages that affect only specific crops, not various crops, and it is difficult to expect high quality and high yield due to abnormal enlargement of crops if the treatment concentration, application time, and application method are different. There is a case. In addition, most of the plant hormones are expensive as imports, and since they are not soluble in water other than gibberellin when preparing the solution, alcohol must be used as a dissolving agent, so that alcohol penetrates into the plant and generates heat, causing the plant to wither.

이를 개선하기 위한 방법 중의 하나로 대한민국 공개특허공보 10-2007-0015528(5-아미노레블린산염, 이의 제조방법 및 이의 용도), 10-2006-0016685(고기능성 작물 생장조절제 및 제초제로서 델타아미노레블린산의 신규한 용도)와 농림부 연구보고서(δ-Aminolevulinic acid (ALA) 작용기작규명 및 생물농약 개발)에서는 유전자 재조합균주에 의해 생성시킨 5-아미노레블린산 또는 5-아미노레블린산염을 이용하여 다양한 작물에 대하여 생장촉진 효과를 밝힌바 있으나, 유전자재조합 균주에 의해 생성된 발효산물은 5-아미노레블린산 이외에 식물생장촉진 인자로 작용할 수 있는 천연의 각종 생리활성물질을 포함하기 힘들다는 특징이 있고, 제조 cost가 높으며, 재조합균주에 의해 생성된 물질을 이용하여 생산될 경우 농산물의 이미지에 악영향을 줄 수 있다는 한계가 있었다.As one of the methods for improving this, Korean Unexamined Patent Publication No. 10-2007-0015528 (5-aminolevulinate, a preparation method thereof and use thereof), 10-2006-0016685 (deltaaminolevulin as a high-functional crop growth regulator and herbicide Novel Use of Acids) and the Ministry of Agriculture Research Report (determining the mechanism of action of δ-Aminolevulinic acid (ALA) and the development of biopesticides) using 5-aminolevulinic acid or 5-aminolevulinate produced by recombinant strains. Although the growth promoting effect has been revealed for various crops, fermented products produced by genetically modified strains are difficult to contain various natural bioactive substances that can act as plant growth promoting factors in addition to 5-aminolevulinic acid. In addition, the manufacturing cost is high, and when produced using the material produced by the recombinant strain, there was a limit that may adversely affect the image of agricultural products All.

따라서 본 발명의 목적은 유산균, 광합성세균, 효모, 바실러스 등 유용미생물에 의한 천연 발효산물을 이용하여 안전하고 사용방법이 간단하며, 경제성 있는 식물 생장촉진용 조성물의 제조방법을 제공하는 것이다.Accordingly, an object of the present invention is to provide a method for preparing a plant growth promoting composition, which is safe and simple to use, and economical using natural fermentation products by useful microorganisms such as lactic acid bacteria, photosynthetic bacteria, yeast, and Bacillus.

상기 본 발명의 목적을 달성하기 위하여, In order to achieve the object of the present invention,

1) 탄소영양원을 약 0.1~2.0중량%, 질소영양원을 0.1~1.0중량%, 인산영양원을 0.01~0.2중량%, 기타 영양원을 0.1~2.0중량%로 한 발효배지를 준비하여 지하수에 용해시킨 후 광합성세균을 접종하여 20~35℃를 유지하면서 3~5일간 배양하여 식물 생장촉진 물질로 알려진 5-아미노레블린산이 함유된 발효산물 1을 얻는다. 표 1에 5-아미노레블린산의 분석방법을 정리한다.1) Prepare fermentation medium containing about 0.1 ~ 2.0% by weight of carbon nutrient source, 0.1 ~ 1.0% by weight of nitrogen nutrient source, 0.01 ~ 0.2% by weight of phosphate nutrient source, and 0.1 ~ 2.0% by weight of other nutrient sources and dissolve in groundwater. Inoculate photosynthetic bacteria and incubate for 3 to 5 days while maintaining 20 ~ 35 ℃ to obtain a fermentation product 1 containing 5-aminolevulinic acid known as plant growth promoting material. Table 1 summarizes the analysis method for 5-aminolevulinic acid.

[표 1]TABLE 1

5-5- 아미노레블린산Aminolevulinic acid 분석  analysis methodmethod 1. 배양상등액 7㎖에 acetic acid buffer(pH 4.6) 2.8㎖과 0.2㎖의 acetylacetone을 첨가한 후 15분간 100℃에서 가열, 냉각하여 2㎖을 채취 2. 채위된 시료에 2㎖에 modified Ehrlich reagent를 가하여 15분간 실온에서 반응시킨 후 553㎚에서 흡광도 측정 가. acetic acid buffer(pH 4.6) : glacial acetic acid 57㎖에 sodium acetate trihydrate 136g을 첨가한 후 D.W. 로 1L를 맞춤. 나. modified Ehrlich reagent : DMAB(ρ-dimethylaminobenzaldehyde) 1g을 glacial acetic acid 42㎖과 70% perchloric acid 8㎖에 녹임1. Add 2.8 ml of acetic acid buffer (pH 4.6) and 0.2 ml of acetylacetone to 7 ml of the culture supernatant, heat and cool at 100 ° C for 15 minutes, and take 2 ml. 2. Modified Ehrlich reagent in 2 ml. After the reaction was conducted for 15 minutes at room temperature, the absorbance was measured at 553 nm. acetic acid buffer (pH 4.6): After adding 136 g of sodium acetate trihydrate to 57 ml of glacial acetic acid, D.W. Fit 1L. I. modified Ehrlich reagent: Dissolve 1 g of DMAB (ρ-dimethylaminobenzaldehyde) in 42 ml of glacial acetic acid and 8 ml of 70% perchloric acid.

2) 탄소영양원을 1~20중량%, 질소영양원을 0.1~1중량%, 인산영양원을 0.01~0.2중량%로 한 발효배지를 준비하여 지하수에 용해시킨 후 유산균 2종, 광합성세균, 효모균, 바실러스균을 혼합 접종하여 20~35℃를 유지하면서 5~20일간 배양하여 유기산 등 다량의 생리활성물질이 함유된 발효산물 2를 얻는다.2) Prepare fermentation medium containing 1 ~ 20% by weight of carbon nutrient source, 0.1 ~ 1% by weight of nitrogen nutrient source, 0.01 ~ 0.2% by weight of phosphate nutrient source, dissolve in groundwater, and then dissolve in lactic acid bacteria, photosynthetic bacteria, yeast, and Bacillus By inoculating the bacteria and incubated for 5 to 20 days while maintaining 20 ~ 35 ℃ to obtain a fermentation product 2 containing a large amount of bioactive substances such as organic acids.

3) 상기 1)의 발효산물 1과 2)의 발효산물 2를 적당한 비율로 혼합하여 식물 생장촉진용 조성물을 제조하는 방법을 제공한다.3) It provides a method for producing a plant growth promoting composition by mixing the fermentation products 1 and 2) fermentation products 2 of 1) in an appropriate ratio.

이하, 본 발명을 상세히 설명한다.Hereinafter, the present invention will be described in detail.

상기 발효배지 중 탄소영양원으로 이용할 수 있는 성분은 포도당, 과당, 맥아당, 당밀, 유당 등이 있고, 질소영양원으로 이용할 수 있는 성분은 펩톤, 트립톤, 우레아, 효모추출물, 말트추출물, 비프추출물 등이 있으며, 인산영양원으로 이 용할 수 있는 성분은 인산칼륨, 인산나트륨 등이 있다.Among the fermentation broths, components that can be used as a carbon nutrient source include glucose, fructose, maltose, molasses, and lactose. The components that can be used as a nitrogen nutrient source are peptone, tryptone, urea, yeast extract, malt extract, beef extract, and the like. The phosphate nutrients can be used as potassium phosphate, sodium phosphate and the like.

본 발명의 접종 미생물 중 광합성세균은 로도슈도모나스속 균, 로도박터속 균, 로도스피릴륨속 균을 이용할 수 있으며, 유산균은 락토바실러스속 균, 루코노스톡속 균, 페디오코커스속 균을 이용할 수 있다.Photosynthetic bacteria of the inoculated microorganism of the present invention can be used Rhodo Pseudomonas bacteria, Rhodobacter bacteria, Rhodophyllium bacteria, Lactobacillus bacteria, Lactobacillus bacteria, Pediococcus bacteria can be used have.

상기 단계 1)의 배양 조건은 통기량을 0.1~0.5vvm으로 유지하여 ORP가 -70~0mv가 되도록 유지시키는 것을 특징으로 한다. Culture conditions of step 1) is characterized in that the ORP is maintained at -70 ~ 0mv by maintaining the aeration amount to 0.1 ~ 0.5vvm.

이하, 본 발명을 실시예에 의해 상세히 설명하고자 한다. 단, 하기 실시예는 본 발명을 예시하는 것일 뿐 본 발명의 권리범위가 이들 실시예에만 한정되는 것은 아니다.Hereinafter, the present invention will be described in detail by way of examples. However, the following examples are only for illustrating the present invention, and the scope of the present invention is not limited only to these examples.

실시예Example : 유용미생물의  Useful microorganisms 발효산물을Fermented products 이용한 식물 생장촉진용 조성물의 생산 Production of plant growth promoting composition using

발효조에 지하수와 포도당 1.0중량%, 효모추출물 0.5중량%, 일인산칼륨 0.05중량%, 이인산나트륨 0.2중량%, 글루탐산나트륨 0.5중량%, 사과산 0.5중량%, 황산암모늄 0.3중량%, 황산마그네슘 0.05중량%에 해당되는 발효배지를 함께 넣어 용해시킨 후 로도슈도모나스속 균을 접종하여 30~35℃를 유지하고 ORP를 -70~0mv를 유지할 수 있도록 통기량을 조절하면서 4일간 배양하여 식물 생장촉진 물질인 5-아미노레블린산이 함유된 발효산물 1을 얻었으며, 표1에 의한 방법으로 5-아미노레블린산을 측정한 결과 1g/L가 함유되어 있음을 확인하였다. 또다른 발효조에 지하수와 당밀 10 중량%, 효모추출물 1중량%, 과당 10중량%에 해당되는 발효배지를 함께 넣어 용해시킨 후 락토바실러스속 균 1종, 루코노스톡속 균 1종, 로도박터속 균 1종, 사카로마이세스속 균 1종, 바실러스속 균 1종을 혼합 접종하고 30~35℃를 유지하면서 10일간 배양하여 뛰어난 생리활성물질, 효소, 항산화물질, 유기산이 다량 함유된 발효산물 2를 얻었다(도2 참조). 그 다음 각 발효산물을 50:50으로 혼합하여 식물 생장촉진용 조성물을 제조하였다.Groundwater and glucose 1.0% by weight, yeast extract 0.5% by weight, potassium monophosphate 0.05% by weight, sodium diphosphate 0.2% by weight, sodium glutamate 0.5% by weight, malic acid 0.5% by weight, ammonium sulfate 0.3% by weight, magnesium sulfate 0.05% by weight After dissolving the fermentation broth together with%, inoculated with Rhodoshudomonas bacteria to maintain 30 ~ 35 ℃ and to control ORP to maintain -70 ~ 0mv by incubating for 4 days while controlling the plant growth material Fermentation product 1 containing 5-aminolevulinic acid was obtained. As a result of measuring 5-aminolevulinic acid by the method according to Table 1, it was confirmed that 1g / L was contained. In another fermentation tank, ground water and molasses, 10% by weight of yeast extract, and 1% by weight of fructose were added together to dissolve, followed by dissolution of one strain of Lactobacillus, one species of genus Lukonostoc, and one of Rhodobacter. Fermented product containing a large amount of excellent bioactive substances, enzymes, antioxidants and organic acids by inoculating 1 species, 1 species of Saccharomyces and 1 species of Bacillus, and incubating for 10 days while maintaining at 30-35 ℃ 2 was obtained (see Fig. 2). Each fermentation product was then mixed at 50:50 to prepare a composition for promoting plant growth.

실험예Experimental Example 1 : 열무의 생육에 대한 효과 1: effect on the growth of young radish

비닐하우스에 75cm*40cm*45cm 원예용포트 3개를 준비하고 원예용 상토[(주)토비테크 : '메리트']와 마사토를 1:1로 섞어서 동일하게 각 포트에 채운 후 열무를 500개체 이상씩 파종하였다. 20~30℃를 유지하면서 일주일 간격으로 1개의 포트는 대조구로서 지하수만을 엽면 살포하였고, 포트 1과 포트 2에는 각각 실시예에 의해 생산된 식물 생장촉진용 조성물의 5,000배 희석액과 10,000배 희석액을 엽면 살포하였다. 21일 후의 식물생장촉진 효과를 확인하여 표 2에 정리하였다. Prepare three 75cm * 40cm * 45cm garden pots in a plastic house, mix gardening clay [Toby Tech Co., Ltd .: 'Merrit'] and Masato 1: 1 and fill each pot equally, and then heat radish more than 500 Sowing was soy. At one week intervals, one pot was sprayed with only groundwater as a control while maintaining a temperature of 20 to 30 ° C. Ports 1 and 2, respectively, were sprayed with 5,000-fold dilutions and 10,000-fold dilutions of the plant growth-promoting compositions produced by the examples. Sprayed. Confirmation of plant growth promoting effect after 21 days was summarized in Table 2.

[표 2]TABLE 2

대조구 (무처리)Control (no treatment) 10,000배 희석액 처리10,000-fold dilution 5,000배 희석액 처리5,000-fold dilution 엽장(cm)Leaf length (cm) 5.25.2 7.87.8 7.67.6 엽폭(cm)Leaf width (cm) 2.72.7 3.43.4 3.53.5 엽수(개)Leaves () 3.13.1 3.43.4 3.23.2 지상부 총무게(g)Ground weight (g) 10.310.3 12.412.4 12.712.7 뿌리길이(cm)Root Length (cm) 5.95.9 6.36.3 6.36.3 지하부 총무게(g)Underground gross weight (g) 4.54.5 6.06.0 6.256.25

표 2의 결과로부터 본 발명의 식물 생장촉진용 조성물이 열무 잎과 뿌리의 생장을 촉진함을 확인하였다. 또한 도 1에 나타난 바와 같이 10,000배 처리구와 5,000배 처리구의 열무가 대조구에 비해 엽록소 함량이 증가되었음을 확인할 수 있다.From the results of Table 2 it was confirmed that the composition for promoting plant growth of the present invention promotes the growth of radish leaves and roots. In addition, as shown in Figure 1 it can be seen that the heat chlorophyll content of 10,000 times treatment and 5,000 times treatment compared to the control.

실험예Experimental Example 2 : 사과의 수확량 및 비대/착색에 대한 효과 2: Effect on apple yield and hypertrophy / coloring

동일한 조건을 가진 5년생 사과나무[품종"후지"] 4그루 중 각각 2그루씩 대조구와 처리구로 선택하였다. 처리구에는 개화한 4월 만개 시부터 7월까지 3주에 1회씩 총 5회에 걸쳐 실시예에 의해 생산된 식물 생장촉진용 조성물의 10,000배 희석액을 엽면 살포하였고 대조구에는 같은 양의 지하수를 엽면 살포하였다. 수확 후 열매의 착색상태, 총 과수량, 무게 등을 비교하여 표 3에 정리하였다.Two out of four five-year-old apple trees [variety "Fuji"] with the same conditions were selected as controls and treatments. The treatment area was sprayed with 10,000-fold dilution of the plant growth promoting composition produced by the example five times, once every three weeks, from full bloom in April to July, and the control area was sprayed with the same amount of groundwater. It was. After harvesting, the coloring status of the fruit, the total amount of fruit, the weight, etc. were compared and summarized in Table 3.

[표 3]TABLE 3

총수확량 (개) Total yield () 총 무게 (kg) Total weight (kg) 착색도(개)Coloring degree () 착색비율 60% 이상60% or more coloring ratio 착색비율 50~59%50 ~ 59% coloring ratio 착색비율 50% 미만Coloration ratio less than 50% 대조구 Control AA 185185 46.2546.25 3232 8787 6666 A'A ' 190190 49.4049.40 3434 9090 6666 처리구 Treatment BB 210210 55.6555.65 5252 9595 6363 B'B ' 200200 55.0055.00 5151 9292 5757

* 착색비율은 전체면적에 대한 착색된 면적의 비율을 말한다. * Coloration ratio is the ratio of the colored area to the total area.

표 3의 결과로부터 본 발명의 식물 생장촉진용 조성물이 사과의 수확량 증대, 착색 및 비대촉진 효과를 나타냄을 확인하였다.From the results of Table 3, it was confirmed that the composition for promoting plant growth of the present invention showed an increase in yield, coloring and hypertrophy of apples.

실험예Experimental Example 3 : 오이의 생육 및 수확량에 대한 효과 3: effect on the growth and yield of cucumbers

비닐하우스에 종묘를 이식한지 1달 된 오이[품명"다다기"]를 각각 대조구와 처리구로 나누어 10일에 1회 처리구에는 실시예에 의해 생산된 식물 생장촉진용 조성물의 10,000배 희석액을 엽면 살포하였고 대조구에는 같은 양의 지하수를 엽면 살포하였 다. 15일간의 수확량을 조사하여 표 4에 정리하였다.One month after transplanting the seedlings (named "Tadada"), which had been transplanted to the plastic house, were divided into control and treatment, and once every 10 days, 10,000-fold dilutions of the plant growth-promoting composition produced by the example were foliarly sprayed. The control area was sprayed with the same amount of groundwater. The yield of 15 days was investigated and summarized in Table 4.

[표 4]TABLE 4

대조구( 무처리 ) (단위 : 개) Control ( Non-treated ) (Unit: pieces) 처리구 (단위 : 개) Treatment Unit (Unit: unit) 1일차Day 1 4545 4646 2일차Day 2 4444 5151 3일차Day 3 4242 5252 4일차Day 4 4545 5151 5일차Day 5 4040 5353 6일자Date 6 3131 4747 7일자Date 7 2525 4747 8일자Date 8 3838 5050 9일자Date 9 3838 5050 10일자Date 10 4040 5252 11일자Date 11 4040 5252 12일자Date 12 4545 5656 13일자Date 13 4444 5656 14일자Date 14 4444 5454 15일자Date 15 4141 5656 합 계Sum 602602 722722

* 상품성 있는 열매만 수확량으로 집계하였음. * Only fruit that is commercially available is counted as the yield.

표 4의 결과로부터 본 발명의 식물 생장촉진용 조성물이 오이의 생육촉진 및 수확량 증대 효과가 있음을 확인하였다.From the results of Table 4 it was confirmed that the composition for promoting plant growth of the present invention has the effect of promoting the growth and yield of cucumber.

실험예Experimental Example 4 : 토마토의 염해에 대한 효과 4: effect on salting of tomatoes

원예용 포트 2개를 준비하고 원예용 상토[(주)토비테크 : '메리트']와 마사토를 1:1로 섞어서 동일한 중량으로 각 포트에 채운 후 토마토 모종을 10포기씩 이식하였다. 두 포트 중 1개의 포트는 처리구로서 실시예에 의해 생산된 식물 생장촉진용 조성물의 5,000배 희석액을 주 1회씩 엽면 살포하였고 대조구 포트는 동일량의 지하수를 엽면 살포하면서 7주간 온실에서 재배하였다. 이때 4주 경과 시점에서 대조구, 처리구의 포트 바닥 배수구멍 20개중 15개를 막고 각 포트에 토양 중량당 1.5 중량%에 상당하는 양의 염화나트륨을 물에 용해시켜 토양에 관주 처리 한 후 나머지 3주동안 토마토의 염해정도를 하기에 기재한 6단계로 평가하여 표 5에 정리하였다.Two horticultural pots were prepared, mixed with horticultural soil [Toby Tech Co., Ltd .: 'Merit'] and Masato 1: 1, and filled in each pot with the same weight, and 10 seedlings of tomato seedlings were transplanted. One of the two pots was sprayed once a week with foliar spray of a 5,000-fold dilution of the plant growth promoting composition produced in Example as a treatment, and the control pot was grown in a greenhouse for 7 weeks while spraying the same amount of groundwater. At this point, after 15 weeks, 15 of 20 port bottom drainage holes of control and treatment ports were blocked, and sodium chloride was dissolved in water in an amount equivalent to 1.5% by weight of soil in each port. The degree of salting of the tomatoes was summarized in Table 5 by evaluating in six steps described below.

■평가단계Evaluation stage

0: 전혀 염해가 보이지 않는다.   0: No salt is seen at all.

1: 전체적으로 매우 약한 염해가 보인다.   1: A very weak salt is seen overall.

2: 3포기 미만에서 약한 염해가 보인다.   2: A weak salt is seen in less than 3 aeration.

3: 5포기 이상에서 명백한 염해가 보인다.   3: Over 5 aerations, apparent salting is seen.

4: 7포기 이상에서 강한 염해가 보인다.   4: Strong salting is seen above 7 aeration.

5: 5포기 이상이 염해에 의해 고사 한다.   5: More than 5 aerations are killed by salting.

[표 5]TABLE 5

대조구(Control ( 무처리No treatment )) 처리구Treatment 염화나트륨 처리 1일차Day 1 Sodium Chloride Treatment 00 00 염화나트륨 처리 3일차Day 3 of Sodium Chloride Treatment 1One 00 염화나트륨 처리 5일차Day 5 of sodium chloride treatment 1One 00 염화나트륨 처리 7주차Week 7 of Sodium Chloride Treatment 22 1One 염화나트륨 처리 9일차Day 9 of Sodium Chloride Treatment 22 1One 염화나트륨 처리 11일차Day 11 of sodium chloride treatment 33 1One 염화나트륨 처리 13주차Week 13 of Sodium Chloride Treatment 33 22 염화나트륨 처리 15일차Day 15 of sodium chloride treatment 44 22 염화나트륨 처리 17일차Day 17 of sodium chloride treatment 44 22 염화나트륨 처리 19일차Day 19 of sodium chloride treatment 55 22 염화나트륨 처리 21일차Day 21 of Sodium Chloride Treatment 55 33

표 5의 결과로부터 본 발명의 식물 생장촉진용 조성물이 토마토의 염해에 대한 내성을 향상시켰음을 확인하였다.From the results in Table 5, it was confirmed that the composition for promoting plant growth of the present invention improved resistance to salting of tomatoes.

실험예Experimental Example 5 : 토마토의 냉해에 대한 효과 5: effect on the coldening of tomatoes

원예용 포트 3개를 준비하고 원예용 상토[(주)토비테크 : '메리트']와 마사토를 1:1로 섞어서 동일한 중량으로 각 포트에 채운 후 토마토 모종을 10포기씩 이식하였다. 두 포트 중 1개의 포트는 처리구로서 실시예에 의해 생산된 식물 생장촉진용 조성물의 5,000배 희석액을 주 1회씩 엽면 살포하였고 대조구 포트는 동일량의 지하수를 엽면 살포하면서 4주간 온실에서 재배하였다. 그리고 대조구와 처리구를 저온(4℃) 조건으로 옮겨 4일간의 냉해정도를 하기에 기재한 6단계로 평가하여 표 6에 정리하였다.Three horticultural pots were prepared, mixed with horticultural soil [Toby Tech Co., Ltd .: 'merit'] and Masato in a 1: 1 weight and filled in each pot, and then 10 tomato seedlings were transplanted. One of the two pots was sprayed once a week with foliar spray of a 5,000-fold dilution of the plant growth promoting composition produced in Example as a treatment and the control pot was grown in a greenhouse for 4 weeks while spraying the same amount of groundwater. And the control and treatment were moved to a low temperature (4 ℃) condition and evaluated the degree of cold thaw of 4 days in six steps described below summarized in Table 6.

■평가단계Evaluation stage

0: 전혀 냉해가 보이지 않는다.   0: There is no cold at all.

1: 전체적으로 매우 약한 냉해가 보인다.   1: Very mild cold overall.

2: 3포기 미만에서 약한 냉해가 보인다.   2: A mild cold sea is seen below 3 aeration.

3: 5포기 이상에서 명백한 냉해가 보인다.   3: Over 5 aerations, apparent cold water is seen.

4: 7포기 이상에서 강한 냉해가 보인다.   4: Strong cold sea is seen at 7 or more wastes.

5: 5포기 이상이 냉해에 의해 고사 한다.   5: Five or more air bubbles die by cold sea.

[표 6]TABLE 6

대조구(Control ( 무처리No treatment )) 처리구Treatment 저온조건 1일차Day 1 of Low Temperature 22 1One 저온조건 2일차Day 2 of cold conditions 33 22 저온조건 3일차Day 3 of cold conditions 55 22 저온조건 4일차Day 4 of low temperature condition 55 33

표 6의 결과로부터 본 발명의 식물 생장촉진용 조성물이 토마토의 냉해에 대한 내성을 향상시켰음을 확인하였다.From the results of Table 6, it was confirmed that the composition for promoting plant growth of the present invention improved resistance to cold damage of tomatoes.

상기 실시예 및 실험예에서 나타난 바와 같이, 본 발명의 식물 생장촉진용 조성물은 식물의 잎과 줄기에 살포 처리하였을 경우 식물체내 엽록소를 증가시켜 잎과 줄기의 색을 진하게 하고 뿌리와 잎의 생장을 촉진하며, 과일의 착색 및 비대를 촉진하고, 저일조·저온·염류집적 등 불량환경 하에서의 식물생장 장애를 예방하는 효과가 있다. 특히 엽록소의 증가는 식물체의 광합성능력을 향상시키는 역할을 하므로 상기 효과 이외에도 다양한 생장촉진효과를 기대할 수 있다.As shown in the above examples and experimental examples, the composition for promoting plant growth according to the present invention increases the chlorophyll in the plant when sprayed on the leaves and stems of the plant to increase the color of the leaves and stems, and to increase the growth of the roots and leaves. It has the effect of promoting the coloring and enlargement of fruits, and preventing plant growth disorders under poor conditions such as low sunshine, low temperature, and salt accumulation. In particular, the increase in chlorophyll plays a role in improving the photosynthetic capacity of the plant, in addition to the above effects can be expected a variety of growth promoting effect.

Claims (3)

일정한 조성의 발효배지에 유용미생물인 광합성세균을 단독 배양하여 식물 생장촉진 물질을 다량 함유한 발효산물 1을 얻고 또 다른 발효배지에 유산균, 광합성세균, 효모, 바실러스 등 다양한 유용미생물을 혼합 접종하여 공생관계를 형성케 함으로써 천연의 생리활성물질, 효소, 항산화물질, 유기산이 다량 함유된 발효산물 2를 얻어 각각 일정한 비율로 혼합함을 특징으로 하는 식물 생장촉진용 조성물의 제조방법.By cultivating the photosynthetic bacteria, which are useful microorganisms in a certain composition, fermentation product 1 containing a large amount of plant growth-promoting substances is obtained. Method for producing a composition for promoting plant growth, characterized in that to obtain a fermentation product 2 containing a large amount of natural physiologically active substances, enzymes, antioxidants, organic acids by mixing to form a relationship. 제 1 항에 있어서, The method of claim 1, 상기 발효산물 1 배양에 사용되는 접종 미생물은 로도슈도모나스속 균, 로도박터속 균, 로도스피릴륨속 균 중에서 1종을 선택하며, 배양 조건은 통기량을 0.1~0.5vvm으로 유지하여 ORP가 -70~0mv가 되도록 배양함으로써 5-아미노레블린산이 0.5~10g/L가 함유됨을 특징으로 하는 식물 생장촉진용 조성물의 제조방법. The inoculated microorganism used in the fermentation product 1 culture is selected from Rhodoschudomonas bacteria, Rhodobacterium bacteria, and Rhodophyllium bacteria, and the culture condition is ORP is -70 by maintaining aeration rate of 0.1 ~ 0.5vvm A method for producing a composition for promoting plant growth, characterized by containing 0.5 to 10 g / L of 5-aminolevulinic acid by culturing to ˜0 mv. 제 1 항에 있어서, The method of claim 1, 상기 발효산물 2에 사용되는 접종미생물 중 광합성세균은 로도슈도모나스속 균, 로도박터속 균, 로도스피릴륨속 균 중에서 1종, 유산균은 락토바실러스속 균, 루코노스톡속 균, 페디오코커스속 균 중에서 2종을 선택하여 배양하는 것을 특징으로 하는 식물 생장촉진용 조성물의 제조방법. Among the inoculated microorganisms used in the fermentation product 2, photosynthetic bacteria are one of the genus Rhodoschudomonas, Rhodobacter, and Rhodophyllium, and the lactic acid bacteria are Lactobacillus, Luconostok, and Pdiococcus. Method for producing a composition for promoting plant growth, characterized in that the culture of two selected from.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20160147022A (en) * 2014-04-28 2016-12-21 아사히 그룹 홀딩스 가부시키가이샤 Method for applying reducible fertilizer to plant body, and agent used in deciduous fruit tree
KR102558135B1 (en) * 2022-03-15 2023-07-24 이승근 Composition for Improving Plant Growth Using Co-culture of Effective Microorganisms

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20160147022A (en) * 2014-04-28 2016-12-21 아사히 그룹 홀딩스 가부시키가이샤 Method for applying reducible fertilizer to plant body, and agent used in deciduous fruit tree
KR102558135B1 (en) * 2022-03-15 2023-07-24 이승근 Composition for Improving Plant Growth Using Co-culture of Effective Microorganisms

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