• 한국균학회지
• /
• 제41권4호
• /
• pp.218-224
• /
• 2013

한국 전통 발효식품에서 분리한 효모로부터 인산 가용화 활성이 우수한 5균주를 선발하였다. 선발한 균주 중 2균주는 Pichia anomala로 동정되었고, 3균주는 각각 Pichia farinosa, Candida versatilis, Pichia subpelliculosa로 동정되었다. 인산 가용화 효모는 $20{\sim}35^{\circ}C$의 온도에서 잘 자라는 중 온성 효모였으며 P. farinosa Y669는 $45^{\circ}C$의 고온에서도 생장하였다. C. versatilis Y907 균주는 pH 5~6의 좁은 pH 범위에서 생장하였고 15%의 NaCl 농도까지 내성을 나타내는 호염성 균주였다. 그 외 4균주는 pH 4.0~8.0에서 생장하였으며 NaCl 10% 농도에서 내성을 나타내었다. 인산 가용화 균주는 토양에서도 8주 동안 $10^7{\sim}10^8$ cfu/g의 밀도를 유지하며 생존하였다. 분리균주 중 인산 가용화 활성은 P. subpelliculosa Y1101가 가장 우수하였으며 배양 11일 후 697.2 ug/mL의 유리인산을 생성하였다.

• 한국토양비료학회지
• /
• 제40권6호
• /
• pp.442-446
• /
• 2007

토양에 고정되어 축적된 난용성 인산염을 가용화하는 유용세균을 선발하여 생물비료로 이용하고자 고추, 토마토, 상추, 오이, 목초, 잔디의 근권토양 및 뿌리표면에서 인산가용화능이 있는 세균을 분리하였다. 선발된 인산가용화균은 16S rRNA 염기서열과 생화학적특성 등에 의해 동정되었으며, 난용성인산 가용화기능이 우수한 세균 Pseudomonas sp. CL-1 및 Kluyvera sp. CL-2균주를 선발하였다. Pseudomonas sp. CL-1균주는 esculin과 gelatin, casein을 가수분해하였고, 그리고 glucose, arabinose, mannose, mannitol, N-acetyl-glucosamine, gluconate, caprate, adipate, malate, citrate 등을 이용하였다. Kluyvera sp. CL-2 균주는 esculin과 CM-cellulose를 가수분해 하였고 acetoin을 생성하였다. 그리고 glucose, arabinose, mannose, mannitol, N-acetyl-glucosamine, maltose, gluconate, malate, citrate 등을 이용하였다. Pikovskaya's medium에서 선발균주의 난용성인산 $Ca_3(PO_4)_2$의 인 가용화량을 정량한 결과 Pseudomonas sp. CL-1과 Kluyvera sp. CL-2 균주는 접종후 1일, 3일에 각각 148.0, $193.4(P\;mg\;L^{-1})$와 482.8 mg, 493.6 mg의 인 가용화량을 나타내었다

• Journal of Ginseng Research
• /
• 제46권1호
• /
• pp.1-10
• /
• 2022

Ginseng has been well-known as a medicinal plant for thousands of years. Bacterial endophytes ubiquitously colonize the inside tissues of ginseng without any disease symptoms. The identification of bacterial endophytes is conducted through either the internal transcribed spacer region combined with ribosomal sequences or metagenomics. Bacterial endophyte communities differ in their diversity and composition profile, depending on the geographical location, cultivation condition, and tissue, age, and species of ginseng. Bacterial endophytes have a significant effect on the growth of ginseng through indole-3-acetic acid (IAA) and siderophore production, phosphate solubilization, and nitrogen fixation. Moreover, bacterial endophytes can protect ginseng by acting as biocontrol agents. Interestingly, bacterial endophytes isolated from Panax species have the potential to produce ginsenosides and bioactive metabolites, which can be used in the production of food and medicine. The ability of bacterial endophytes to transform major ginsenosides into minor ginsenosides using β-glucosidase is gaining increasing attention as a promising biotechnology. Recently, metabolic engineering has accelerated the possibilities for potential applications of bacterial endophytes in producing beneficial secondary metabolites.

• Journal of Microbiology and Biotechnology
• /
• 제21권6호
• /
• pp.556-566
• /
• 2011

A total of 31 Acinetobacter isolates were obtained from the rhizosphere of Pennisetum glaucum and evaluated for their plant-growth-promoting traits. Two isolates, namely Acinetobacter sp. PUCM1007 and A. baumannii PUCM1029, produced indole acetic acid (10-13 ${\mu}g$/ml). A total of 26 and 27 isolates solubilized phosphates and zinc oxide, respectively. Among the mineral-solubilizing strains, A. calcoaceticus PUCM1006 solubilized phosphate most efficiently (84 mg/ml), whereas zinc oxide was solubilized by A. calcoaceticus PUCM1025 at the highest solubilization efficiency of 918%. All the Acinetobacter isolates, except PUCM1010, produced siderophores. The highest siderophore production (85.0 siderophore units) was exhibited by A. calcoaceticus PUCM1016. Strains PUCM1001 and PUCM1019 (both A. calcoaceticus) and PUCM1022 (Acinetobacter sp.) produced both hydroxamate-and catechol-type siderophores, whereas all the other strains only produced catechol-type siderophores. In vitro inhibition of Fusarium oxysporum under iron-limited conditions was demonstrated by the siderophore-producing Acinetobacter strains, where PUCM1018 was the most potent inhibitor of the fungal phytopathogen. Acinetobacter sp. PUCM1022 significantly enhanced the shoot height, root length, and root dry weights of pearl millet seedlings in pot experiments when compared with controls, underscoring the plant-growth-promoting potential of these isolates.

• Journal of Applied Biological Chemistry
• /
• 제52권3호
• /
• pp.116-120
• /
• 2009

본 연구에서는 생물농약용으로 연구 개발된 길항미생물의 균주들을 이용하여 친환경농업용 길항미생물 컨소시엄을 개발하고자 하였으며, 개별 길항미생물의 항생능력, 항진균성 siderophore 및 ${\beta}$-glucannase 생산능, auxin생산능, 인산가용능 등 각 기작별 상호 보완형 미생물균주의 컨소시엄 후보군을 구성하였다. 구성된 컨소시엄 후보군 중 컨소시엄 No. 11이 in vivo pot test에서 가장 좋은 고추생장촉진능과 교추역병 방제능을 발휘하였다. 최적 컨소시엄인 No. 11 컨소시엄내 두 길항미생물인 B. subtilis AH18과 B. licheniformis K11은 기작별 상호보완형으로 모두 auxin생산능, 항진균성siderophore 및 ${\beta}$-glucannase생산능을 가지며, 특히 B. licheniformis K11는 고추역병을 길항하는 항생물질인 iturin을 생산한다. 고추역병방제용 최적컨소시엄 구성균주들간의 상호 비경쟁적 상리공생 여부를 조사하기 위하여 개별균주인 B. subtilis AH18과 B. licheniformis K11을 각각 단독으로 배양한 것과 두 균주를 동시에 접종하여 배양한 것 그리고, 각각 단독으로 배양한 것을 접종시에 혼용하는 것의 3가지 처리를 실시하였다. 그 결과 동시 배양한 것은 각각을 단독을 배양한 것과 비교하였을 때 방제능과 생육촉진능 모두 시너지 효과를 나타내지 않았다. 하지만, 단독배양 후 혼용한 처리구에서는 시너지 효과를 크게 나타내었는데 방제능도 가지면서 뿌리, 줄기, 잎의 생장촉진효과에서 모두 개별 단독배양 후 처리 또는 동시배양 후 처리에서 보다 50% 이상 시너지 효과를 발휘하였다.

• 한국미생물·생명공학회지
• /
• 제49권3호
• /
• pp.403-412
• /
• 2021

본 연구에서는 토양 및 근권에 존재하는 Bacillus 속의 식물 생장 촉진 활성, 식물 병원성 곰팡이의 생장 억제활성, 미네랄 가용화능 및 세포 외 효소활성을 확인해 보고자 하였다. 식물 병원성 곰팡이에 대한 항진균 활성에서 DDP257은 10종의 병원성 곰팡이에서 항진균 활성이 모두 나타났다. 식물 생장 촉진 인자인 indole-3-acetic acid 생성능에서는 ANG20이 70.97 ㎍/ml로 가장 높게 나타났다. 추가적으로 1-aminocyclopropane-1-carboxylate deaminase 생성능 조사에서는 총 10종에서 생성능을 확인하였고, 질소 고정능과 siderophore 생성능 조사에서는 대부분의 분리균주에서 활성을 확인하였다. 이후 분리된 균주에 대하여 phosphate, calcite, zinc과 같은 미네랄 가용화능을 확인하였으며 세포외 효소활성에서도 대부분의 효소에서 활성이 나타났다. 특히 alkaline phosphatase, esterase (C4), acid phosphatase, naphtol-AS-BI-phosphohydrolase에서 선별된 균주 모두 유사한 활성을 보였다. 이는 Bacillus 속이 다양한 유기물과 항생물질 및 세포 외 효소를 분비함으로써 이러한 결과가 나타난 것으로 판단된다. 따라서, 본 연구 결과를 통해 토양의 환경 개선에 기여하는 균주를 활용하여 미생물 제제로써의 가능성을 제시한다.

• 한국토양비료학회지
• /
• 제35권1호
• /
• pp.59-67
• /
• 2002

강한 인산 가용력을 가진 인산 용해 세균인 균주 60-2G를 잔디의 근권에서 분리하였다. GC-FAME구조와 탄소이용형태 및 16S rRNA의 부분 염기서열 분석을 통해 균주 60-2G는 Enterobacter intermedium으로 동정되었다. Hydroxyapatite를 첨가한 배지와 생장 시킨 균주 60-2G는 gluconic acid 와 2-ketogluconic acid 및 소량의 lactic acid를 생성하였다. 균주 60-2G의 생장 기간동안 배지의 pH는 3.8 까지 낮아지는 반면에 배지의 유효 인산 농도는 증가하였다. 배지의 낮은 pH와 유효인산농도의 증가는 역 상관관계이며, 이는 균주 60-2G가 생성하는 유기산에 의한 영향이다. E. intermedium 60-2G 균주는 유기산 생성에 관여하는 glucose dehydrogenase의 co-factor인 PQQ를 생성하였으며, pqq의 부분 염기서열 분석 결과 기존에 보고된 서열과 85% 이상의 상동성을 가지고 있었다.

• Journal of Microbiology and Biotechnology
• /
• 제27권3호
• /
• pp.480-491
• /
• 2017

Fluorescent pseudomonads have been isolated from halophytes, mesophytes, and xerophytes of Pakistan. Among these, eight isolates, GS-1, GS-3, GS-4, GS-6, GS-7, FS-2 (cactus), ARS-38 (cotton), and RP-4 (para grass), showed antifungal activity and were selected for detailed study. Based on biochemical tests and 16S rRNA gene sequences, these were identified as strains of P. chlororaphis subsp. chlororaphis and aurantiaca. Secondary metabolites of these strains were analyzed by LC-MS. Phenazine-1-carboxylic acid (PCA), 2-hydroxy-phenazine, Cyclic Lipopeptide (white line-inducing principle (WLIP)), and lahorenoic acid A were detected in variable amounts in these strains. P. aurantiaca PB-St2 was used as a reference as it is known for the production of these compounds. The phzO and PCA genes were amplified to assure that production of these compounds is not an artifact. Indole acetic acid production was confirmed and quantified by HPLC. HCN and siderophore production by all strains was observed by plate assays. These strains did not solubilize phosphate, but five strains were positive for zinc solubilization. Wheat seedlings were inoculated with these strains to observe their effect on plant growth. P. aurantiaca strains PB-St2 and GS-6 and P. chlororaphis RP-4 significantly increased both root and shoot dry weights, as compared with uninoculated plants. However, P. aurantiaca strains FS-2 and ARS-38 significantly increased root and shoot dry weights, respectively. All strains except PB-St2 and ARS-38 significantly increased the root length. This is the first report of the isolation of P. aurantiaca from cotton and cactus, P. chlororaphis from para grass, WLIP and lahorenoic acid A production by P. chlororaphis, and zinc solubilization by P. chlororaphis and P. aurantiaca.

• BMB Reports
• /
• 제29권3호
• /
• pp.253-260
• /
• 1996

An enzyme that hydrolyzes flavin-adenine dinucleotide (FAD) was found to be present in rat liver lysosomal membrane prepared from Triton WR-1339 filled lysosomes (tritosomes) purified by flotation on sucrose. This FAD phosphohydrolase (FADase) exhibited optimal activity at pH 8.5 and had an apparent Km of approximately 3.3 mM. The activity was decreased 50~70% by dialysis against EDTA and this was restored by $Zn^{2+}$, $Mg^{+2}$, $Hg^{+2}$, and $Ca^{+2}$ ions inhibited the enzyme, but $F^-$ and molybdate had no effect. The enzyme was also inhibited by p-chloromercuribenzoate (pCMB), reduced glutathione and other thiols, cyanide, and ascorbate. The presence of ATP, ADP, AMP. ${\alpha}-{\beta}-methylene$ ATP, AMP-p-nitrophenyl phosphate (PNP), GMP, and coenzyme A (CoA) decreased the activity on FAD, but pyrimidine nucleotides, adenosine, adenine, or $NAD^+$ were without effect. Phosphate stimulated the activity slightly. FAD phosphohydrolase activity was separated from ATPase and inorganic pyrophosphatase activities by solubilization with detergents and polyacrylamide gel electrophoresis and by linear sucrose density gradient centrifugation suggesting that the enzyme is different from ATPase, inorganic pyrophosphatase, and soluble lysosomal FAD pyrophosphatase. Paper chromatography showed that FAD was hydrolyzed to flavin mononucleotide (FMN) and AMP which were further hydrolyzed to riboflavin and AMP by phosphatases known to be present in lysosomal membranes. Incubation of the intact Iysosomes with pronase showed that the active site of FAD phosphohydrolase must be oriented to the cytosol. The FAD hydrolyzing activity was detected in Golgi, microsome, and plasma membrane, but not in mitochondria or soluble lysosomal preparations.

• 한국토양비료학회지
• /
• 제49권1호
• /
• pp.17-29
• /
• 2016

Though there is an abundant supply of nitrogen in the atmosphere, it cannot be used directly by the biological systems since it has to be combined with the element hydrogen before their incorporation. This process of nitrogen fixation ($N_2$-fixation) may be accomplished either chemically or biologically. Between the two elements, biological nitrogen fixation (BNF) is a microbiological process that converts atmospheric di-nitrogen ($N_2$) into plant-usable form. In this review, the genetics and mechanism of nitrogen fixation including genes responsible for it, their types and role in BNF are discussed in detail. Nitrogen fixation in the different agricultural systems using different methods is discussed to understand the actual rather than the potential $N_2$-fixation procedure. The mechanism by which the diazotrophic bacteria improve plant growth apart from nitrogen fixation such as inhibition of plant ethylene synthesis, improvement of nutrient uptake, stress tolerance enhancement, solubilization of inorganic phosphate and mineralization of organic phosphate is also discussed. Role of diazotrophic bacteria in the enhancement of nitrogen fixation is also dealt with suitable examples. This mini review attempts to address the importance of diazotrophic bacteria in nitrogen fixation and plant growth improvement.