Kangming Tian

ORCID: 0009-0007-5648-8286
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Microbial Metabolic Engineering and Bioproduction
  • Enzyme Catalysis and Immobilization
  • Biofuel production and bioconversion
  • Enzyme Production and Characterization
  • Bacterial Genetics and Biotechnology
  • Enzyme Structure and Function
  • Viral Infectious Diseases and Gene Expression in Insects
  • Protein Hydrolysis and Bioactive Peptides
  • Gene Regulatory Network Analysis
  • RNA and protein synthesis mechanisms
  • Peptidase Inhibition and Analysis
  • Proteins in Food Systems
  • Bacteriophages and microbial interactions
  • Animal Genetics and Reproduction
  • Microplastics and Plastic Pollution
  • biodegradable polymer synthesis and properties
  • Microbial Metabolites in Food Biotechnology
  • Graphene and Nanomaterials Applications
  • Food Chemistry and Fat Analysis
  • Heat shock proteins research
  • Alcoholism and Thiamine Deficiency
  • Food composition and properties
  • Analytical Chemistry and Chromatography
  • Studies on Chitinases and Chitosanases
  • Recycling and Waste Management Techniques

Tianjin University of Science and Technology
2014-2024

Durban University of Technology
2021

Jiangnan University
2010-2013

L-Lactic acid, one of the most important chiral molecules and organic acids, is produced via pyruvate from carbohydrates in diverse microorganisms catalyzed by an NAD+-dependent L-lactate dehydrogenase. Naturally, Escherichia coli does not produce noticeable amounts, but can catabolize it a dehydrogenation reaction mediated FMN-dependent In aims to make E. strain L-lactate, three dehydrogenase genes different bacteria were cloned expressed. The producing strains, 090B1 (B0013-070,...

10.1186/1475-2859-13-78 article EN cc-by Microbial Cell Factories 2014-01-01

Current commercial production of isomalto-oligosaccharides (IMOs) commonly involves a lengthy multistage process with low yields. To improve the efficiency for IMOs, we developed simple and efficient method by using enzyme cocktails composed recombinant Bacillus naganoensis pullulanase produced licheniformis, α-amylase from amyloliquefaciens, barley bran β-amylase, α-transglucosidase Aspergillus niger to perform simultaneous saccharification transglycosylation liquefied starch. After 13 h...

10.1016/j.ejbt.2016.12.002 article EN cc-by-nc-nd Electronic Journal of Biotechnology 2016-12-13

Biodiesel has attracted considerable attention as one of the best choices among alternative and renewable fuels. Large quantities crude glycerol are produced a main co-product with increasing biodiesel production. Currently, problem waste utilization needs to be crucially addressed, not only for environmental protection but also economy industry. In this paper, use production D-lactate by engineered Escherichia coli was investigated. Engineered E. B0013-070 homolactic pathway synthesis...

10.1039/c3gc41769g article EN Green Chemistry 2013-11-07

Lignocellulosic ethanol could offer a sustainable source to meet the increasing worldwide demand for fuel. However, efficient and simultaneous metabolism of all types sugars in lignocellulosic hydrolysates by ethanol-producing strains is still challenge. An engineered strain Escherichia coli B0013-2021HPA with regulated glucose utilization, which use monosaccharides except cell growth production, was constructed. In E. B0013-2021HPA, pta-ackA, ldhA pflB were deleted block formation acetate,...

10.1186/s12934-018-0915-x article EN cc-by Microbial Cell Factories 2018-05-02

Escherichia coli strain CICIM B0013 was genetically engineered to efficiently produce optically pure D-lactate (higher than 99.9%) from glycerol with a minimum of by-products. When E. coli B0013-070 (DackA, Dpta, Dpps, DpflB, Ddld, DpoxB, DadhE,DfrdA) was cultivated aerobically for 9 h followed by 27 under microaerobic fermentation, it produced 98.5 g l-1 of no more 2 l-1 total by-products glycerol. During the phase, the average productivity and yield were 3.45 l-1 h-1 and 64 g/100 glycerol,...

10.5897/ajb11.3464 article EN AFRICAN JOURNAL OF BIOTECHNOLOGY 2012-03-13

Burdock (Arctium lappa L.) is a fructan-rich plant with prebiotic potential. The aim of this study was to develop an efficient enzymatic route prepare fructooligosaccharides (FOS)-rich and highly antioxidative syrup using burdock root as raw material. Endo-inulinase significantly improved the yield FOS 2.4-fold while tannase pretreatment further increased 2.8-fold. Other enzymes, including endo-polygalacturonase, endo-glucanase endo-xylanase, were able increase total soluble sugar by 11.1%...

10.1016/j.ejbt.2019.04.009 article EN cc-by-nc-nd Electronic Journal of Biotechnology 2019-05-15

Efficient production of D-lactate by engineered Escherichia coli entails balancing cell growth and product synthesis. To develop a metabolic switch to implement desirable transition from fermentation, thiamine auxotroph B0013-080A was constructed in highly efficient producer E. strain B0013-070. This achieved inactivation thiE, gene encoding phosphate synthase for biosynthesis monophosphate. The resultant mutant failed grow on the medium absence yet restored when exogenous provided. A linear...

10.1002/bit.25699 article EN Biotechnology and Bioengineering 2015-07-07

Abstract Ammonium hydroxide is conventionally used as an alkaline reagent and cost-effective nitrogen source in enzyme manufacturing processes. However, few ammonia-inducible expression systems have been described thus far. In this study, genomic-wide transcriptional changes Bacillus licheniformis CBBD302 cultivated media supplemented with ammonia were analyzed, resulting identification of 1443 differently expressed genes, which 859 genes upregulated 584 downregulated. Subsequently, the...

10.1093/jimb/kuab037 article EN cc-by Journal of Industrial Microbiology & Biotechnology 2021-06-01

Bacillus licheniformis is a well-known platform strain for production of industrial enzymes. However, the development genetically stable recombinant B. high-yield enzyme still laborious. Here, pair plasmids, pUB-MazF and pUB'-EX1, were firstly constructed. thermosensitive, self-replicable plasmid. It was able to efficiently cure from host cell through induced expression an endoribonuclease MazF, which lethal cell. pUB'-EX1 nonreplicative integrative Its replication dependent on...

10.1093/jimb/kuac009 article EN cc-by-nc-nd Journal of Industrial Microbiology & Biotechnology 2022-03-19
Coming Soon ...