Shengqiu Feng

Dr. Shengqiu Feng


Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 July 2017 in Plant Biotechnology Journal
Verified
Journal Article
Open access
PDF file
CFChunfen Fan
Chunfen Fan
YLYing Li
Ying Li
ZHZhen Hu
Zhen Hu
HHHuizhen Hu
Huizhen Hu
GWGuangya Wang
Guangya Wang
SFShengqiu Feng
Shengqiu Feng
Summary: Plant lodging resistance is an important integrative agronomic trait of grain yield and quality in crops. Although extensin proteins are tightly associated with plant cell growth and cell wall construction, little has yet been reported about their impacts on plant lodging resistance. In this study, we isolated a novel extensin‐like (OsEXTL) gene in rice, and selected transgenic rice plants that expressed OsEXTL under driven with two distinct promoters. Despite different OsEXTL expression levels, two‐promoter‐driven OsEXTL‐transgenic plants, compared to a rice cultivar and an empty vector, exhibited significantly reduced cell elongation in stem internodes, leading to relatively shorter plant heights by 7%–10%. Meanwhile, the OsEXTL‐transgenic plants showed remarkably thickened secondary cell walls with higher cellulose levels in the mature plants, resulting in significantly increased detectable mechanical strength (extension and pushing forces) in the mature transgenic plants. Due to reduced plant height and increased plant mechanical strength, the OsEXTL‐transgenic plants were detected with largely enhanced lodging resistances in 3 years field experiments, compared to those of the rice cultivar ZH11. In addition, despite relatively short plant heights, the OsEXTL‐transgenic plants maintain normal grain yields and biomass production, owing to their increased cellulose levels and thickened cell walls. Hence, this study demonstrates a largely improved lodging resistance in the OsEXTL‐transgenic rice plants, and provides insights into novel extensin functions in plant cell growth and development, cell wall network construction and wall structural remodelling.

21 March 2018 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
YLYing Li
Ying Li
PLPeng Liu
Peng Liu
JHJiangfeng Huang
Jiangfeng Huang
RZRan Zhang
Ran Zhang
ZHZhen Hu
Zhen Hu
Liangcai PengLiangcai Peng
Liangcai Peng
Rice is a major food crop containing large amounts of lignocellulose residues usable for biofuels. In this study, we collected transgenic rice plants that over-produced Trichoderma reesei β-1,4-D-glucosidase (BGL I) into the cell walls in the mature straws. Without any pretreatment, the transgenic rice straws showed a consistently higher biomass enzymatic saccharification than the wild-type (WT) cultivar, in particular when 1% Tween-80 or 0.5% PEG-4000 was co-supplied into the enzymatic hydrolysis. Notably, under mild alkali pretreatment (1% NaOH at 50 °C for 2 h), the desirable transgenic line exhibited complete biomass enzymatic hydrolysis, resulting in the highest bioethanol yield of 21% (% dry matter) when compared with the rice and other bioenergy crops subjected to stronger pretreatment conditions reported in previous studies. Meanwhile, despite relatively low hexose yields obtained under 1% H2SO4 pretreatment, the transgenic rice straw also showed high bioethanol production at 18% due to an almost complete sugar–ethanol conversion rate. Chemical analyses indicated that the transgenic rice straw had significantly increased biomass porosity and reduced cellulose features (CrI, DP), which contributed to the largely enhanced biomass enzymatic hydrolysis. In addition, the raised arabinose level in hemicellulose and the lignin H-monomer proportion may also positively affect the biomass enzymatic saccharification in the transgenic rice straw. Hence, this study demonstrated a cost-effective and green lignocellulose conversion technology for high bioethanol production in the transgenic rice straw. It also provided a strategy for the potential genetic modification of plant cell walls in bioenergy crops.

Verified
Journal Article
Open access
PDF file
CFChunfen Fan
Chunfen Fan
GWGuangya Wang
Guangya Wang
YWYoumei Wang
Youmei Wang
RZRan Zhang
Ran Zhang
YWYanting Wang
Yanting Wang
Liangcai PengLiangcai Peng
Liangcai Peng
Grain size and weight are two important determinants of grain yield in rice. Although overexpression of sucrose synthase (SUS) genes has led to several improvements on cellulose and starch-based traits in transgenic crops, little is reported about SUS enhancement of hull size and grain weight in rice. In this study, we selected transgenic rice plants that overexpressed OsSUS1-6 genes driven with the maize Ubi promoter. Compared to the controls (wild type and empty vector line), all independent OsSUS homozygous transgenic lines exhibited considerably increased grain yield and grain weights. Using the representative OsSUS3 overexpressed transgenic plants, four independent homozygous lines showed much raised cell numbers for larger hull sizes, consistent with their enhanced primary cell wall cellulose biosynthesis and postponed secondary wall synthesis. Accordingly, the OsSUS3 transgenic lines contained much larger endosperm volume and higher starch levels than those of the controls in the mature grains, leading to increased brown grain weights by 15–19%. Hence, the results have demonstrated that OsSUS overexpression could significantly improve hull size and grain weight by dynamically regulating cell division and starch accumulation in the transgenic rice.

1 February 2015 in Bioresource Technology
Verified
Journal Article
Closed access
LWLeiming Wu
Leiming Wu
MLMeng Li
Meng Li
JHJiangfeng Huang
Jiangfeng Huang
HZHui Zhang
Hui Zhang
WZWeihua Zou
Weihua Zou
SFShengqiu Feng
Shengqiu Feng

12 June 2024 in Science Bulletin
Verified
Journal Article
Closed access
YAYuanhang Ai
Yuanhang Ai
HWHailang Wang
Hailang Wang
PLPeng Liu
Peng Liu
HYHua Yu
Hua Yu
MSMengdan Sun
Mengdan Sun
Liangcai PengLiangcai Peng
Liangcai Peng

1 March 2020 in Carbohydrate Polymers
Verified
Journal Article
Closed access
CFChunfen Fan
Chunfen Fan
GWGuangya Wang
Guangya Wang
LWLeiming Wu
Leiming Wu
PLPeng Liu
Peng Liu
JHJiangfeng Huang
Jiangfeng Huang
SFShengqiu Feng
Shengqiu Feng