scholarly journals Overexpression of Soybean Isoflavone Reductase (GmIFR) Enhances Resistance to Phytophthora sojae in Soybean

2015 ◽  
Vol 6 ◽  
Author(s):  
Qun Cheng ◽  
Ninghui Li ◽  
Lidong Dong ◽  
Dayong Zhang ◽  
Sujie Fan ◽  
...  
Keyword(s):  
Phytophthora Sojae ◽  
Soybean Isoflavone ◽  
Isoflavone Reductase

scholarly journals An FYVE-Domain-Containing Protein, PsFP1, Is Involved in Vegetative Growth, Oxidative Stress Response and Virulence of Phytophthora sojae

2021 ◽  
Vol 22 (12) ◽  
pp. 6601
Author(s):  
Jinhui Zhang ◽  
Xiaoran Du ◽  
Xin Zhou ◽  
Duo Jin ◽  
Jianqiang Miao ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Membrane Trafficking ◽  
Vegetative Growth ◽  
Genome Mining ◽  
Gene Replacement ◽  
Wide Distribution ◽  
Stress Sensitivity ◽  
Phytophthora Sojae ◽  
Knock Out ◽  
Fyve Domain

Proteins that contain the FYVE zinc-finger domain are recruited to PtdIns3P-containing membranes, participating in numerous biological processes such as membrane trafficking, cytoskeletal regulation, and receptor signaling. However, the genome-wide distribution, evolution, and biological functions of FYVE-containing proteins are rarely reported for oomycetes. By genome mining of Phytophthora sojae, two proteins (PsFP1 and PsFP2) with a combination of the FYVE domain and the PX domain (a major phosphoinositide binding module) were found. To clarify the functions of PsFP1 and PsFP2, the CRISPR/Cas9-mediated gene replacement system was used to knock out the two genes respectively. Only heterozygous deletion mutants of PsFP1 were recovered, and the expression level of PsFP1 in the heterozygous knockout transformants was significantly down-regulated. These PsFP1 mutants showed a decrease in mycelial growth and pathogenicity and were more sensitive to hydrogen peroxide. These phenotypes were recovered to the level of wild-type by overexpression PsFP1 gene in the PsFP1 heterozygous knockout transformant. In contrast, deletion of PsFP2 had no significant effect on vegetative growth, asexual and sexual reproduction, pathogenicity, or oxidative stress sensitivity. PsFP1 was primarily localized in vesicle-like structures and both the FYVE and PX domains are important for its localization. Overall, our results indicate that PsFP1 plays an important role in the vegetative growth and virulence of P. sojae.

scholarly journals A CRISPR/Cas9‐mediated in situ complementation method for Phytophthora sojae mutants

2021 ◽  
Vol 22 (3) ◽  
pp. 373-381
Author(s):  
Min Qiu ◽  
Yaning Li ◽  
Wenwu Ye ◽  
Xiaobo Zheng ◽  
Yuanchao Wang
Keyword(s):  
Phytophthora Sojae

Identification of three closely linked loci conferring broad-spectrum Phytophthora sojae resistance in soybean variety Tosan-231

2021 ◽  
Author(s):  
Jun-ichi Matsuoka ◽  
Mami Takahashi ◽  
Tetsuya Yamada ◽  
Yuhi Kono ◽  
Naohiro Yamada ◽  
...  
Keyword(s):  
Broad Spectrum ◽  
Phytophthora Sojae ◽  
Soybean Variety

Analysis of pathogenicity and genetic variation among Phytophthora sojae isolates using RAPD

1999 ◽  
Vol 103 (2) ◽  
pp. 173-178 ◽  
Author(s):  
X.Q. Meng ◽  
R.C. Shoemaker ◽  
X.B. Yang
Keyword(s):  
Genetic Variation ◽  
Phytophthora Sojae

Borrelidin, a Potent Antifungal Agent: Insight into the Antifungal Mechanism against Phytophthora sojae

2012 ◽  
Vol 60 (39) ◽  
pp. 9874-9881 ◽  
Author(s):  
Ya-Mei Gao ◽  
Xiang-Jing Wang ◽  
Ji Zhang ◽  
Ming Li ◽  
Chong-Xi Liu ◽  
...  
Keyword(s):  
Antifungal Agent ◽  
Phytophthora Sojae ◽  
Antifungal Mechanism ◽  
Insight Into

scholarly journals A Novel Thermostable GH3β-Glucosidase fromTalaromyce leycettanuswith Broad Substrate Specificity and Significant Soybean Isoflavone Glycosides-Hydrolyzing Capability

2018 ◽  
Vol 2018 ◽  
pp. 1-9
Author(s):  
Xinxin Li ◽  
Wei Xia ◽  
Yingguo Bai ◽  
Rui Ma ◽  
Hong Yang ◽  
...  
Keyword(s):  
Amino Acid ◽  
Glycoside Hydrolase ◽  
Animal Feed ◽  
Amino Acid Residues ◽  
Calculated Molecular Mass ◽  
Substrate Specificities ◽  
Soybean Isoflavone ◽  
Food Animal ◽  
Isoflavone Glycoside ◽  
Hydrolysis Rates

A novelβ-glucosidase gene (Bgl3B) of glycoside hydrolase (GH) family 3 was cloned from the thermophilic fungusTalaromyce leycettanusJM12802 and successfully expressed inPichia pastoris. The deduced Bgl3B contains 860 amino acid residues with a calculated molecular mass of 91.2 kDa. The purified recombinant Bgl3B exhibited maximum activities at pH 4.5 and 65°C and remained stable at temperatures up to 60°C and pH 3.0−9.0, respectively. The enzyme exhibited broad substrate specificities, showingβ-glucosidase, glucanase, cellobiase, xylanase, and isoflavone glycoside hydrolase activities, and its activities were stimulated by short-chain alcohols. The catalytic efficiencies of Bgl3B were 693 and 104/mM/s towardspNPG and cellobiose, respectively. Moreover, Bgl3B was highly effective in converting isoflavone glycosides to aglycones at 37°C within 10 min, with the hydrolysis rates of 95.1%, 76.0%, and 75.3% for daidzin, genistin, and glycitin, respectively. These superior properties make Bgl3B potential for applications in the food, animal feed, and biofuel industries.

scholarly journals Genetic Mapping and Molecular Characterization of a Broad-spectrum Phytophthora sojae Resistance Gene in Chinese Soybean

2019 ◽  
Vol 20 (8) ◽  
pp. 1809 ◽  
Author(s):  
Chao Zhong ◽  
Yinping Li ◽  
Suli Sun ◽  
Canxing Duan ◽  
Zhendong Zhu
Keyword(s):  
Genetic Mapping ◽  
Candidate Gene ◽  
Broad Spectrum ◽  
Genomic Region ◽  
Phytophthora Sojae ◽  
Genetic Population ◽  
Phytophthora Root Rot ◽  
Different Origins ◽  
Lrr Domain

Phytophthora root rot (PRR) causes serious annual soybean yield losses worldwide. The most effective method to prevent PRR involves growing cultivars that possess genes conferring resistance to Phytophthora sojae (Rps). In this study, QTL-sequencing combined with genetic mapping was used to identify RpsX in soybean cultivar Xiu94-11 resistance to all P. sojae isolates tested, exhibiting broad-spectrum PRR resistance. Subsequent analysis revealed RpsX was located in the 242-kb genomic region spanning the RpsQ locus. However, a phylogenetic investigation indicated Xiu94-11 carrying RpsX is distantly related to the cultivars containing RpsQ, implying RpsX and RpsQ have different origins. An examination of candidate genes revealed RpsX and RpsQ share common nonsynonymous SNP and a 144-bp insertion in the Glyma.03g027200 sequence encoding a leucine-rich repeat (LRR) region. Glyma.03g027200 was considered to be the likely candidate gene of RpsQ and RpsX. Sequence analyses confirmed that the 144-bp insertion caused by an unequal exchange resulted in two additional LRR-encoding fragments in the candidate gene. A marker developed based on the 144-bp insertion was used to analyze the genetic population and germplasm, and proved to be useful for identifying the RpsX and RpsQ alleles. This study implies that the number of LRR units in the LRR domain may be important for PRR resistance in soybean.

Sign in / Sign up

Export Citation Format

Share Document