Range Of Molecular Weight Distribution Research Articles

Characterization and functional evidence for Orf2 of Streptomyces sp. 139 as a novel dipeptidase E

Aspartyl dipeptidase (dipeptidase E) can hydrolyze Asp-X dipeptides (where X is any amino acid), and the enzyme plays a key role in the degradation of peptides as nutrient sources. Dipeptidase E remains uncharacterized in Streptomyces. Orf2 from Streptomyces sp. 139 is located in the exopolysaccharide biosynthesis gene cluster, which may be a novel dipeptidase E with “S134-H170-D198” catalytic triad by sequence and structure comparison. Herein, recombinant Orf2 was expressed in E. coli and characterized dipeptidase E activity using the Asp-ρNA substrate. The optimal pH and temperature for Orf2 are 7.5 and 40 ℃; Vmax and Km of Orf2 are 0.0787 mM·min−1 and 1.709 mM, respectively. Orf2 exhibits significant degradation activities to Asp-Gly-Gly, Asp-Leu, Asp-His, and isoAsp-Leu and minimal activities to Asp-Pro and Asp-Ala. Orf2 contains a Ser-His-Asp catalytic triad characterized by point mutation. In addition, the Asp147 residue of Orf2 is also proven to be critical for the enzyme’s activity through molecular docking and point mutation. Transcriptome analysis reveals the upregulation of genes associated with ribosomes, amino acid biosynthesis, and aminoacyl-tRNA biosynthesis in the orf2 mutant strain. Compared with the orf2 mutant strain and WT, the yield of crude polysaccharide does not change significantly. However, crude polysaccharides from the orf2 mutant strain exhibit a wider range of molecular weight distribution. The results indicate that the Orf2 links nutrient stress to secondary metabolism as a novel dipeptidase E.Key points• A novel dipeptidase E with a Ser-His-Asp catalytic triad was characterized from Streptomyces sp. 139.• Orf2 was involved in peptide metabolism both in vitro and in vivo.• Orf2 linked nutrient stress to mycelia formation and secondary metabolism in Streptomyces.

Response mechanism of soil leachate and disinfection by-product formation to extreme precipitation events under continuous drought scenario

In this study, a rainfall simulation device was employed to investigate the response mechanism of soil leachate and disinfection by-products formation potential (DBPsFP) to extreme precipitation events. The results revealed that the aromaticity of dissolved organic matter (DOM) and the concentration of hydrophobic DOM containing aromatic carbon groups in leachate decreased with rising temperature. The humification degree of DOM decreased at 25 °C (99 mm/h), while the humification degree and protein-like level of DOM increased under high temperatures droughts (45 °C and 65 °C). Higher temperatures resulted in the leach of more microbial-derived humus and low molecular phenolic compounds from soil and broadened the range of molecular weight distribution. Increasing temperature increased DBPsFP and DBPs species and caused the precursors of haloacetic acids (HAAs) in leachate to become more hydrophobic, while the precursors of trihalomethanes (THMs) became more hydrophilic. Most importantly, the increased temperature attenuated the rainfall-mediated dilution of organic pollutant concentration, and temperature has a more significant effect than extreme rainfall in DOM abundance and the formation potential (or species) of DBPs. The results help to better understand the impact of climate change on the physicochemical processes of water quality.

Structural, functional and mechanistic insights uncover the role of starch in foxtail millet cultivars with different congee-making quality

Ten foxtail millet cultivars with different congee-making quality were investigated for relationships between starch structures, functional properties and congee-making qualities. Swelling power, pasting peak viscosity (PV) and setback (SB), gel hardness and resilience, and gelatinization onset (To), peak (Tp) and range (R) temperature were correlated with congee-making performance significantly. Good eating-quality cultivars with these parameters were in the range of 15.41–18.58 %, 3095–3279 cp, 1540–1745 cp, 430–491 g, 0.47–0.57, 64.43–65.28 °C, 69.97–70.32 °C and 23.38–24.52 °C, respectively. Correlation analysis showed that amylose, amylopectin B2 chains and A21 were essential parameters controlling the functional properties. Amylose molecules with linear molecular morphology would cause crystal defects and a wide range of molecular weight distribution. Additionally, they were more prone to re-association, which influenced the PV, SB, To, Tp and gel hardness. B2 chains impacted the gelatinization temperature range (R), gel resilience and swelling behavior by affecting the alignment of double helices and the size of starch particles and pores. Starch with more binding sites of bound water (A21) tended to leach from the swelling granules easily and contributed to higher values of PV. The content of amylose, B2 chains and A21 of good eating-quality cultivars were 16.19–18.46 %, 11.60–11.69 % and 96.50–97.02 %, respectively.

Analysis and control of products obtained from pyrolysis of polypropylene using a reflux semi-batch reactor and GC-MS/FID and FT-ICR MS

Pyrolysis of plastic waste allows to produce liquid fractions, but their molecular weight distributions are typically very large whereas it would be interesting to focus on light hydrocarbons. In this study, the pyrolysis of polypropylene (PP) was investigated using a semi-batch, vertical glass reactor heated at 480 °C equipped with a reflux condenser. The pyrolysis was performed with and without a reflux condenser. The temperature at the top of this reflux condenser was ranged from 125 °C to 200 °C depending on the heating power at the wall of this condenser. The permanent gas yield (C1 to C4) ranged between 20.9 wt% and 25.8 wt% when the reflux was used. The gas contained mainly hydrocarbons with a carbon range from C1 to C4 and H2 in a smaller extent. Their kinetic profiles followed a similar trend, i.e they exhibited a maximum with time. The GC-MS/FID detected mainly olefinic hydrocarbons (olefins) with less than 28 carbons. The major hydrocarbons obtained were light and heavy naphtha cuts when the reflux was used. The range of light naphtha (C5-C7) was between 13.1 and 16.7 wt% and the range of heavy naphtha (C8-C12) was between 69.1 and 87.2 wt% of the total mass fraction detected. The experiments demonstrated that the presence of the reflux has a significant impact on the liquid and gas yields. It allows to narrow the molecular weight distribution range of the liquid, which was confirmed by FT-ICR MS. As a consequence, the molecules of interest are maximised, especially those corresponding to the naphtha cuts.

Thermo- and Light-Responsive Polymer-Coated Magnetic Nanoparticles as Potential Drug Carriers.

A series of thermo- and light-responsive copolymers of poly (N-isopropylacrylamide) (PNIPAM) and 6-[4-(4-methoxy phenyl azo)-phenoxyl-hexyl methacrylate) (AzoMA) (PNIPAM-b-PAzoMA) were synthesized via reversible addition–fragmentation chain transfer (RAFT) radical polymerization. The resulting copolymers had a narrow molecular weight distribution range of 1.06–1.24, in which M n changed regularly with the monomer concentration. Subsequently, the diblock copolymers were successfully modified on the surface of iron oxide nanoparticles through the interaction between the chemical bonds to prepare Fe3O4@(PNIPAM-b-PAzoMA) nanoparticles. The size of fabricated nanoparticles with excellent thermo-sensitivity and photo-sensitivity was controlled at about 40–50 nm. Cell viability assays suggested that the nanoparticles showed no significant cytotoxicity and potential drug delivery in the tumor microenvironment.

Suppression of Chain Transfer at High Temperature in Catalytic Olefin Polymerization

AbstractLiving polymerization by suppressing chain transfer is a very useful method for achieving precise molecular weight and structure control. However, the suppression of chain transfer at high temperatures is extremely challenging in any catalytic polymerization. This has been a severe limitation for catalytic olefin polymerization, which is one of the most important chemical reactions. Here, we report the unprecedented living polymerization of ethylene at 130 °C, with a narrow molecular weight distribution range of 1.04 to 1.08. This is a significant increase in the reaction temperature. Tailor‐made α‐diimine nickel catalysts that exhibit both the steric shielding and fluorine effects play an essential role in this breakthrough. These nickel catalysts are even active at 200 °C, and enable the formation of semi‐crystalline, ultrahigh‐molecular‐weight polyethylene at 150 °C. Mechanistic insights into the key chain transfer reaction are elucidated by density functional theory calculations.

Suppression of Chain Transfer at High Temperature in Catalytic Olefin Polymerization

Living polymerization by suppressing chain transfer is a very useful method for achieving precise molecular weight and structure control. However, the suppression of chain transfer at high temperatures is extremely challenging in any catalytic polymerization. This has been a severe limitation for catalytic olefin polymerization, which is one of the most important chemical reactions. Here, we report the unprecedented living polymerization of ethylene at 130 °C, with a narrow molecular weight distribution range of 1.04 to 1.08. This is a significant increase in the reaction temperature. Tailor-made α-diimine nickel catalysts that exhibit both the steric shielding and fluorine effects play an essential role in this breakthrough. These nickel catalysts are even active at 200 °C, and enable the formation of semi-crystalline, ultrahigh-molecular-weight polyethylene at 150 °C. Mechanistic insights into the key chain transfer reaction are elucidated by density functional theory calculations.

Production and Chemical Characterization of Exopolysaccharides by Antarctic Yeasts Vishniacozyma victoriae and Tremellomycetes sp.

The study aimed to investigate exopolysaccharides (EPSs) produced by two Antarctic yeasts isolated from Livingston Island. The species were identified as Vishniacozyma victoriae (V) and Tremellomycetes sp. (T) based on a molecular genetic analysis of ITS1-5.8S-ITS4 regions of the 18S rRNA gene. The EPS production was investigated under stress conditions in culture flasks and a bioreactor. Different chromatographic (HPLC-RID, HPSEC-RID) and spectral (FT-IR) analyses were employed to characterize EPSs. Tremellomycetes sp. accumulated 7 g/L biomass and 4.5 g/L EPS after 120 h of cultivation. The total carbohydrate content of V-EPS and T-EPS was 75.4% and 79.0%, respectively. The EPSs mainly consisted of mannose (30–32%), which was followed by glucose, xylose, galactose, and small amounts of uronic acids (6.3–7.0%). EPSs had appreciable amounts of proteins (11–12%). The FT-IR spectra contained absorption bands typical for hetero-mannans and β-glucans (797–1033 cm−1). EPSs were heterogeneous with a broad molecular weight distribution range (47 × 104–68 × 104 g/mol). In conclusion, both yeasts synthesized high-molecular-weight heteromannans, and Tremellomycetes sp. stood out as being a better producer than V. victoriae. The current study also formed a basis for a better assessment of the potential for practical application of EPSs and yeasts in biochemical engineering and biotechnology.

Feasibility Study of Gelatin Preparation from the Bioinspired Collagen Aggregates by a "Two-step" Facile Degradation Method.

Gelatin is the putative research hotspot of natural products, but gelatin prepared by traditional alkali methods has seriously affected its applications due to the worryingly low molecular weight and poor gel strength. Herein, we took the lead to extract the distinct gelatin from a kind of bioinspired collagen aggregate (CA) by a two-step controlled degradation method. Structural analysis suggested that the CA better preserves the natural aggregated structure of nature collagen (typical D-periodic cross-striated pattern). Compared with the gelatin gelatinized by the conventional alkali method (G-Al) and commercial gelatin (CG), the gelatin (G-CA) from CA had a wide molecular weight distribution range, high transparency, high viscosity, and strong gel strength as expected. Meanwhile, the G-CA film exhibited better mechanical performance and thermostability than CG and G-Al films, and water vapor permeability was also higher in the G-CA film, whereas water solubility was higher in the CG and G-Al films. Thus, the G-CA film is more conducive to the use of food packaging or edible films, exhibiting more potential market application prospects. Notably, G-CA based on CA from waste hide offal provides a way to reuse leather waste resources and further realize green and clean production in leather industry.

Lignin extraction from waste biomass with deep eutectic solvents: Molecular weight and heating value

Abstract Separating lignin from cellulose in biomass is a necessary pretreatment step prior to converting them to biofuels or bioproducts. If byproducts from food production can be separated in an ecofriendly solvent at low pressures, biomass specifically grown for biorefining will not need to be shipped long distances. Using deep eutectic solvents (DES) can separate out lignin from the non-food components remaining after agricultural production. This work investigated the efficacy of three DES on four food processing residues on lignin separation, characterizing the molecular weight and fuel value of the extracted lignins. DES pretreatments reduced molecular weight and increased the molecular weight distribution range (PDI) compared to the control black liquor derived lignin. The DES acetic acid: choline chloride (AACC) was most effective for reducing molecular weight and increasing PDI for rice husks and sugarcane bagasse, but a lactic acid: choline chloride DES improved these properties for coffee chaff, and formic acid: choline chloride DES improved them for corn stover. Higher heating values that were higher than the control black liquor derived lignin were found for lignins extracted from rice husks, sugarcane bagasse, and corn stover with AACC.

Surface water treatment benefits from the presence of algae: Influence of algae on the coagulation behavior of polytitanium chloride

Titanium-based coagulation has proved to be effective for algae-laden micro-polluted water purification processes. However, the influence of algae inclusion in surface water treatment by titanium coagulation is barely reported. This study reports the influence of both Microcystis aeruginosa and Microcystis wesenbergii in surface water during polytitanium coagulation. Jar tests were performed to evaluate coagulation performance using both algae-free (controlled) and algae-laden water samples, and floc properties were studied using a laser diffraction particle size analyzer for online monitoring. Results show that polytitanium coagulation can be highly effective in algae separation, removing up to 98% from surface water. Additionally, the presence of algae enhanced organic matter removal by up to 30% compared to controlled water containing only organic matter. Polytitanium coagulation achieved significant removal of fluorescent organic materials and organic matter with a wide range of molecular weight distribution (693–4945 Da) even in the presence of algae species in surface water. The presence of algae cells and/or algal organic matter is likely to function as an additional coagulant or flocculation aid, assisting polytitanium coagulation through adsorption and bridging effects. Although the dominant coagulation mechanisms with polytitanium coagulant were influenced by the coagulant dosage and initial solution pH, algae species in surface water could enhance the charge neutralization capability of the polytitanium coagulant. Algae-rich flocs were also more prone to breakage with strength factors approximately 10% lower than those of algae-free flocs. Loose structure of the flocs will require careful handling of the flocs during coagulation-sedimentation-filtration processes.

Fabrication of starch blend films with different matrices and their mechanical properties

The objective of the study was to determine the effects of molecular sizes of amylose (AM) and starch granules on the mechanical properties of thermoplastic starch (TPS) blend films. Leached amylose solution from cassava (CS_ AM) and mung bean (MB_AM), and two forms of amylopectin (AP) (granular; g and non-granular; ng) of waxy cassava (WxCS) starch were used. Four types of film matrices were fabricated and all TPS blend films contained same amount of AM and glycerol. Results displayed that molecular weight profiles of starch films and presence of granule remnants significantly controlled the film matrix formation, types of crystal formation, and percent of relative crystallinity (%RC) (p < 0.05). Tensile property of TPS films was controlled by %RC and presence of granule remnants. Percent elongation at break (%Eb) of TPS films increased when the films had a large range of molecular weight distribution (from 5.5 × 107 g/mol to 0.4 × 105 g/mol) and contained a high weight fraction (~58%) of starch molecules with Mw~0.4 × 105 g/mol.

Recognition and characterization of active fractions from petroleum sulfonate

Petroleum sulfonates are widely used in chemical flooding in China. The samples are complicated and not all the fractions are effective. To recognize effective fraction with excellent interfacial activity and emulsifying property, a preparative liquid chromatography technology was adopted to perform the fraction separation for petroleum sulfonate. Structural composition, interfacial activity，emulsifying property and flooding efficiency of obtained fractions were also analyzed and discussed. It was shown that petroleum sulfonate can be effectively separated into different fractions with obvious structural differences, among which one fraction with the most excellent interfacial activity and the emulsifying property was recognized. The average molecular weight and molecular weight distribution range of this active fraction were 455.5 and 428–468, respectively, which are both crucial for activities. Alkylbenzene dicyclohexane sulfonates, alkyl indan sulfonates, and alkyl naphthalene sulfonates are major structure types, and alkyl chain length is mainly distributed between 12–15, 15–17 and 15–17 respectively. Besides, this active fraction is universal, and it can produce ultralow interfacial tension (~10−3 mN/m) and good emulsifying property against different crude oils including Xinjiang, Changqing, Liaohe Oilfields, etc. in China. The developed technology herein can be used to track and confirm the characteristics and/or active fraction in petroleum sulfonate accurately.

Fabricating mechanically improved silk-based vascular grafts by solution control of the gel-spinning process

There is a large unmet need for off-the-shelf biomaterial options to supplant venous autografts in bypass and reconstructive surgical procedures. Existing graft alternatives formed from non-degradable synthetic polymers are not capable of maintaining long-term patency and are thus not indicated for <6 mm inner diameter bypass procedures. To fill this void, degradable silk-based biomaterials have been proposed that can maintain their mechanical properties (i.e. compliance) while facilitating slow but progressive biomaterial remodeling and host integration mediated by cellular colonization. The goal of the present study was to enhance the porosity of gel-spun silk tubes, to facilitate faster degradation rates and improve cellularity, and thus improve host integration over time in vivo, while maintaining requisite mechanical functions. Silk solutions with a range of molecular weight distributions and, in turn, viscosities were used to generate tubes of varying porosities. A decrease in solution concentration correlated with an increase in mean pore size and overall porosity through a density-dependent mechanism. Tubes were mechanically analyzed, and these properties were the basis of an analytical model used to correlate tube formulations to structural compliance, which were shown to be similar to the saphenous vein. Tubes were also tested for suture retention to ensure surgical utility despite increased porosity. Tubes were implanted in the abdominal aorta of Sprague-Dawley rats via an end-to-end anastomosis model. Tubes with higher porosities showed early improvements in cell colonization that progressively increased over time; conversely, the dense architecture of less porous grafts (20MB) inhibited cell ingrowth and resulted in minimal biomaterial degradation at the 6-month time point. None of the highly porous tubes (5 MB and 10MB) remained patent at 6 months, likely due remodeling inducing bulk mechanical failure or a compromised blood-material interface.

Optimization of Hydrolysis Conditions for the Isolation of Angiotensin-I Converting Enzyme (ACE) Inhibitory Peptides from Rhopilema hispidum

To obtain the maximum angiotensin-I converting enzyme (ACE) inhibitory activity, the protein hydrolysis conditions of the jellyfish Rhopilema hispidum were optimized using response surface methodology (RSM). Trypsin was selected to produce R. hispidum protein hydrolysates (RPH) with ACE inhibitory activity. The optimal parameters for producing protein hydrolysates with the highest ACE inhibitory activity were as follows: hydrolysis time 5 h, hydrolysis temperature 50°C, and the enzyme-to-substrate ratio 6%. Under these conditions, the ACE inhibitory rate of RPH could reach 64.28% ± 5.72%. In addition, RPH contained high levels of Gly, Glu, Pro, Ala, Asp and Arg, with a molecular weight distribution range of 0.32–6.84 kDa. The following three novel ACE inhibitory peptides were isolated and identified: Ile-Gly-Glu-Thr-Gly-Pro, Gly-Ala-Thr-Gly-Pro-Ala-Gly-Tyr-Val and Gly-Ala-Phe-Gly-Pro-Gly-Gly-Leu-Val-Gly-Arg-Pro. The IC50 values of the ACE inhibitory activity of these three purified peptides were 19.07, 27.42 and 31.26 μmol L−1, respectively. These results suggested that proteins and peptides isolated from R. hispidum could be utilized as antihypertensive functional food sources.

Preparation, characterization of polysaccharides fractions from Inonotus obliquus and their effects on α-amylase, α-glucosidase activity and H2O2-induced oxidative damage in hepatic L02 cells

In the present study, three homogeneous protein bounded acidic polysaccharides fractions (IOPS-1, IOPS-2 and IOPS-5) were isolated from I. obliquus using DEAE-52 cellulose chromatography. The relationship between their physicochemical properties and bioactivities was comparatively investigated. Results showed that IOPS-1, IOPS-2 and IOPS-5 were composed of rhamnose, arabinose, xylose, mannose, glucose and galactose with the molecular weight distribution range from 75.94 kDa to 114.30 kDa. Congo red assay and CD spectra revealed that these three polysaccharides had ordered triple-helical conformations. Among the three polysaccharides, IOPS-2 exhibited the highest enzymes inhibitory activity and protective effects against the H2O2 induced oxidative damages in hepatic L02 cells, which would be related to its specific molecular weight (97.12 kDa), protein and uronic acid contents, rough appearance and triple-helical conformation. These results might facilitate the development of polysaccharides from I. oblqiuus as alternative antioxidants and provide significant insights into the relationship of structure-bioactivity of natural polysaccharides.

Extensive chemical characterization of a heavy fuel oil

This paper presents procedures for determining the fractions, chemical compositions and combustion characteristics of Heavy Fuel Oil (HFO). This chemical characterization is requisite for better prediction of thermodynamic behaviour of multicomponent fuel such as HFO which consist of thousands of different components. Detailed chemical and physical compositions, molecular weight range and mean molecular weight of individual fractions of fuel enable to use more advanced approaches such as continuous thermodynamics for simulation and modelling. Sequential elution solvent chromatography was used to separate a HFO into Saturates, Aromatics, Resins and Asphaltenes (SARA) as gas chromatographic analysis was unsatisfactory to reveal the overall composition of a HFO, due to the insufficient volatility in most of the heavy compounds. Subsequent mass spectrometric and elemental analysis showed a wide range of molecular weight distributions for the fractions. The results also indicate that the saturates fraction contains cyclic structures with aliphatic side chains while the aromatics fraction contains tetracyclic aromatic rings with aliphatic side chains. The degree of difference between the Thermo-Gravimetric Analysis (TGA) scans of the fractions in inert and oxidizing atmospheres observed at high temperatures also increases with the degree of functionality of the fractions due to the presumably greater extent of free radical chemistry occurring in an oxidizing environment. The Infrared spectra of the fractions are consistent with what would be expected from a consideration of the solvents used to elute them in column chromatography and supported the classification of the fractions.

Effects of pH, conductivity, host cell protein, and DNA size distribution on DNA clearance in anion exchange chromatography media.

Flowthrough anion exchange chromatography is commonly used as a polishing step in downstream processing of monoclonal antibodies and other therapeutic proteins to remove process‐related impurities and contaminants such as host cell DNA, host cell proteins, endotoxin, and viruses. DNA with a wide range of molecular weight distributions derived from Chinese Hamster Ovary cells was used to advance the understanding of DNA binding behavior in selected anion exchange media using the resin (Toyopearl SuperQ‐650M) and membranes (Mustang® Q and Sartobind® Q) through DNA spiking studies. The impacts of the process parameters pH (6–8), conductivity (2–15 mS/cm), and the potential binding competition between host cell proteins and host cell DNA were studied. Studies were conducted at the least and most favorable experimental conditions for DNA binding based on the anticipated electrostatic interactions between the host cell DNA and the resin ligand. The resin showed 50% higher DNA binding capacity compared to the membrane media. Spiking host cell proteins in the load material showed no impact on the DNA clearance capability of the anion exchange media. DNA size distributions were characterized based on a “size exclusion qPCR assay.” Results showed preferential binding of larger DNA fragments (>409 base pairs). © 2017 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers Biotechnol. Prog., 34:141–149, 2018

Tunable Large Pore Mesoporous Carbons for the Enhanced Adsorption of Humic Acid.

Tunable large pore soft templated mesoporous carbons (SMC) were obtained via the organic self-assembly of resorcinol/formaldehyde with the triblock copolymer F127 and by investigating the effect of carbon precursor to surfactant (p/s) ratio and carbonization temperature on the material characteristics. The p/s ratio and carbonization temperature were varied respectively from 0.83 to 0.25 and from 400 to 1200 °C. The resulting SMCs had various average pore sizes, tunable from 7 up to 50 nm. At lower p/s ratios, the pore size increased, pore size distributions broadened, and pore volumes increased. An increase of hydrophobicity was observed at elevated carbonization temperatures. A 2D hexagonal ordered SMC with a narrow pore size distribution was obtained at a ratio of 0.83. Lower ratios (0.5 and 0.25) transformed into disordered porous carbons containing micropores, mesopores, and even macropores. The SMCs were tested for adsorption of a large organic molecule, humic acid (HA), from water. The material characteristics that significantly affected HA adsorption capacity were pore size and mass % (wt %) carbon. The novel SMCs showed an unprecedented high adsorption of HA in the entire molecular weight distribution range. SMCs with large mesopores resulted in higher maximum adsorption capacities and improved HA adsorption kinetics compared to activated carbon.

Synthesis of well-defined telechelic trans-1,4-polyisoprene by oxidative cleavage

Synthesis of telechelic trans-1,4-polyisoprenes (TPI: trans-structure > 95%) was evaluated based on two different methods of oxidative cleavage (indirect cleavage: first epoxidation of TPI, then the selective cleavage of epoxidized units in epoxidized trans-1,4-polyisoprene (ETPI) and direct cleavage of isoprene units in TPI). The influence of solvents and the ratio of oxidative agents was investigated by 1H-NMR and 13C-NMR. A series of well-defined telechelic TPI with double terminated functional groups and less side reaction (molecular weight distribution range: 1.96?2.26) were synthesized by indirect cleavage in chloroform. Telechelic TPI showed similar crystallization behavior with TPI and interesting cold crystallization behavior characterized by DSC.