Xiang Gao

Prof. Dr. Xiang Gao

Shaanxi University of Science & Technology
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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1 February 2008 in Phytochemistry
Verified
Journal Article
Closed access
ZZZhongchun Zhang
Zhongchun Zhang
XGXiang Gao
Xiang Gao
BQBaosheng Qiu
Baosheng Qiu

1 September 2006 in Plant and Cell Physiology
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Journal Article
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XGXiang Gao
Xiang Gao
FRFeng Ren
Feng Ren
YLYingtang Lu
Yingtang Lu
Plant salt tolerance is a complex trait involving many genes. To identify new salt tolerance determinants during seed germination, we have screened a population of chemically inducible activation-tagged Arabidopsis mutants. A mutant, designated stg1 ( s alt t olerance during g ermination 1 ), was obtained. The stg1 mutant is less sensitive than the wild type to NaCl and osmotic stress inhibition of germination in the presence of the inducer. Germination assays on media containing various salts upon inducer application indicate that the stg1 mutation enhances tolerance to Na + and K + . Under salt stress, stg1 maintains a higher K + /Na + ratio and accumulates less proline than the wild-type control, suggesting that its salt tolerance mechanisms are mainly involved in the regulation of ion balance. STG1 encodes a putative Arabidopsis TATA box-binding protein (TBP)-associated factor 10 (atTAF10), which constitutes the transcriptional factor IID (TFIID) complex. Overexpression of atTAF10 under the control of the 35S promoter in Arabidopsis improves seed tolerance to salt stress during germination and the knocked-down mutant is more sensitive to salt stress, indicating the transcription initiation factor as a physiological target of salt toxicity in plants.

1 November 2004 in Biotechnology Letters
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Journal Article
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XPXue-Wu Pan
Xue-Wu Pan
HXHeng-Hao Xu
Heng-Hao Xu
XLXin Liu
Xin Liu
XGXiang Gao
Xiang Gao
YLYingtang Lu
Yingtang Lu

27 February 2021 in Marine Drugs
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Journal Article
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XGXiang Gao
Xiang Gao
XJXin Jing
Xin Jing
XLXufeng Liu
Xufeng Liu
PLPeter Lindblad
Peter Lindblad
Scytonemin is a promising UV-screen and antioxidant small molecule with commercial value in cosmetics and medicine. It is solely biosynthesized in some cyanobacteria. Recently, its biosynthesis mechanism has been elucidated in the model cyanobacterium Nostoc punctiforme PCC 73102. The direct precursors for scytonemin biosynthesis are tryptophan and p-hydroxyphenylpyruvate, which are generated through the shikimate and aromatic amino acid biosynthesis pathway. More upstream substrates are the central carbon metabolism intermediates phosphoenolpyruvate and erythrose-4-phosphate. Thus, it is a long route to synthesize scytonemin from the fixed atmospheric CO2 in cyanobacteria. Metabolic engineering has risen as an important biotechnological means for achieving sustainable high-efficiency and high-yield target metabolites. In this review, we summarized the biochemical properties of this molecule, its biosynthetic gene clusters and transcriptional regulations, the associated carbon flux-driving progresses, and the host selection and biosynthetic strategies, with the aim to expand our understanding on engineering suitable cyanobacteria for cost-effective production of scytonemin in future practices.

15 November 2017 in Applied and Environmental Microbiology
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Journal Article
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WLWen Liu
Wen Liu
LCLijuan Cui
Lijuan Cui
HXHaiyan Xu
Haiyan Xu
ZZZhaoxia Zhu
Zhaoxia Zhu
XGXiang Gao
Xiang Gao
A dense exopolysaccharide (EPS) matrix is crucial for cyanobacterial survival in terrestrial xeric environments, in which cyanobacteria undergo frequent expansion and shrinkage processes during environmental desiccation-rehydration cycles. However, it is unclear how terrestrial cyanobacteria coordinate the structural dynamics of the EPS matrix upon expansion and shrinkage to avoid potential mechanical stress while benefiting from the matrix. In the present study, we sought to answer this question by investigating the gene expression, protein dynamics, enzymatic characteristics, and biological roles of WspA, an abundantly secreted protein, in the representative terrestrial cyanobacterium Nostoc flagelliforme . The results demonstrated that WspA is a novel β-galactosidase that facilitates softening of the EPS matrix by breaking the polysaccharide backbone under substantial moisture or facilitates the thickening and relinkage of the broken matrix during the drying process, and thus these regulations are well correlated with moisture availability or desiccation-rehydration cycles. This coordination of flexibility and rigidity of the cyanobacterial extracellular matrix may contribute to a favorable balance of cell growth and stress resistance in xeric environments. IMPORTANCE How the exopolysaccharide matrix is dynamically coordinated by exoproteins to cope with frequent expansion and shrinkage processes in terrestrial colonial cyanobacteria remains unclear. Here we elucidated the biochemical identity and biological roles of a dominant exoprotein in these regulation processes. Our study thus gained insight into this regulative mechanism in cyanobacteria to combat periodic desiccation. In addition, the filamentous drought-adapted cyanobacterium Nostoc flagelliforme serves as an ideal model for us to explore this issue in this study.

1 September 2010 in Phycologia
Verified
Journal Article
Closed access
YLYinghui Liu
Yinghui Liu
LYLan Yu
Lan Yu
WKWenting Ke
Wenting Ke
XGXiang Gao
Xiang Gao
BQBaosheng Qiu
Baosheng Qiu
Liu Y., Yu L., Ke W., Gao X. and Qiu B. 2010. Photosynthetic recovery of Nostoc flagelliforme (Cyanophyceae) upon rehydration after 2 years and 8 years dry storage. Phycologia 49: 429–437. DOI: 10.2216/09-01.1 The photosynthetic recovery of Nostoc flagelliforme (Berkeley & Curtis) Bornet & Flahault upon rehydration was investigated with the 2-year and 8-year dried samples. It was found that the 2-year sample absorbed water much faster compared with the 8-year sample during 3–24-h rehydration. The 2-year sample recovered its photosynthesis and respiration fully upon 24-h rehydration. However, the 8-year sample almost lost its ability to recover dark respiration, net photosynthetic activity, maximal quantum yield and photosystem II (PSII) electron transport activity. The F645/F685 ratio of the 8-year sample increased significantly from 1.70 to 3.09 during 24-h rehydration, which suggested damage to the coupling between phycobiliprotein and the PSII reaction centers. The 8-year sample retained PSI a...